SciELO - Scientific Electronic Library Online

vol.39 número1Hereditary hemochromatosis: An opportunity for gene therapyVesicular transport of Fe and interaction with other metal ions in polarized Caco2 Cell monolayers índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados




Links relacionados


Biological Research

versión impresa ISSN 0716-9760

Biol. Res. v.39 n.1 Santiago  2006 


Biol Res 39: 125-142, 2006


Gene expression profiling in wild-type and metallothionein mutant fibroblast cell lines


1 Department of Nutritional Science and Toxicology, University of California, Berkeley, Berkeley, CA 94720
2 Laboratorio de Bioinformática y Expresión Génica. Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, Santiago, Santiago, Chile

Dirección para Correspondencia


The role of metallothioneins (MT) in copper homeostasis is of great interest, as it appears to be partially responsible for the regulation of intracellular copper levels during adaptation to extracellular excess of the metal. To further investigate a possible role of MTs in copper metabolism, a genomics approach was utilized to evaluate the role of MT on gene expression. Microarray analysis was used to examine the effects of copper overload in fibroblast cells from normal and MT I and II double knock-out mice (MT-/-). As a first step, we compared genes that were significantly upregulated in wild-type and MT-/- cells exposed to copper. Even though wild-type and mutant cells are undistinguishable in terms of their morphological features and rates of growth, our results show that MT-/- cells do not respond with induction of typical markers of cellular stress under copper excess conditions, as observed in the wild-type cell line, suggesting that the transcription initiation rate or the mRNA stability of stress genes is affected when there is an alteration in the copper store capacity. The functional classification of other up-regulated genes in both cell lines indicates that a large proportion (>80%) belong to two major categories: 1) metabolism; and 2) cellular physiological processes, suggesting that at the transcriptional level copper overload induces the expression of genes associated with diverse molecular functions. These results open the possibility to understand how copper homeostasis is being coordinated with other metabolic pathways.

Key terms: copper homeostasis, metallothionein, microarray


Copper is an essential nutrient that is a structural part in some proteins and part of the electron transfer system in many redox-enzymes involved in processes such as respiration, iron metabolism, and neurotransmitter biosynthesis (Uauy et al., 1999). Although essential metals are normally present in trace amounts in the cell, their levels can increase following environmental or nutritional changes. Metal overload can be toxic to the cell, causing a range of effects and leading to cell death when concentrations are extremely high (Pulido and Parrish, 2003; Oteíza et al., 2004; Leonard et al., 2004). To avoid metal-induced toxicity, most organisms have developed several cellular mechanisms of protection. Three general mechanisms, which typically work in combination for effective detoxification, include: reduction of metal uptake; enhanced metal export; and metal sequestration mechanisms (Dameron and Harrison, 1998). The third mechanism, the intracellular chelation or sequestration of metals into less reactive complexes or organelles to limit their toxicity, is a commonly used mechanism. In mammalian systems, excess metals, in particular copper, are partially detoxified by sequestration in the metal-binding metallothioneins (Dameron and Harrison, 1998; Bremner and Beattie, 1990; Nordberg, 1989).

Metallothioneins (MTs) are a class of low molecular weight, intracellular and cysteine-rich proteins that have high affinity for metal ions (Cousins, 1983; Park et al., 2001; Coyle et al., 2002). MT gene sequences are highly conserved in a wide range of species from bacteria to humans, which is a suggestive feature of a protein with a high biological importance. MTs have unique structural characteristics for their potent metal-binding and redox capabilities. Although the members of this family were discovered nearly 40 years ago, a primary role has not been identified, and new functions continue to be discovered (Palmiter, 1998). Currently, MTs are known to be involved in metal ion homeostasis and detoxification, protection against oxidative damage, cell proliferation and apoptosis, chemoresistance, and radiotherapy resistance (Palmiter, 1998; Coyle et al., 2002). MT expression has been implicated as a transient response to any form of stress or injury and may provide cytoprotective action. Four major MT isoforms _ MT I, MT II, MT III, and MT IV _ have been identified in mammals (Coyle et al., 2002; Theocharis et al., 2003). MT I and MT II are the two major forms in mammals; they are expressed in most tissues and stages of development. The analysis of mice with altered gene expression of MT I and II has enhanced our understanding of the multifaceted role of MT. MT I/II double knockout (MT-/-) mice demonstrated that MT expression is not essential for the normal development, growth, or reproductive capacity of these mice (Klaassen and Liu, 1998). These mutant mice and the cell lines derived from them have been used extensively in recent years to investigate the role of MT. Most results show that animals or cells lacking MT I/II are more sensitive to a wide range of stressors, such as oxidative stress; excess metals, such as cadmium, lead, copper and zinc; and infectious and inflammatory agents (Zheng et al., 1996; Kelly et al.,1996; Kelly and Palmiter, 1996; Liu et al., 1999; Rojas and Klaassen, 1999; Liu et al., 2000; Qu et al., 2002).

The role of MT in copper homeostasis is of great interest, as it appears to be responsible for the regulation of intracellular copper levels during adaptation to extracellular copper excess. It has been shown that MT protects cells against elevated levels of extracellular copper (Freedman and Peisach, 1989; Kawai et al., 2000). As copper toxicity involves its ability to catalyze the generation of free radicals and/or to directly interact with essential biomolecules, copper sequestering by MT is of critical importance for cell protection. Besides serving to detoxify excess copper, MT may play a role in normal copper metabolism, although currently this role is unknown.

In a recent study, we demonstrated notable changes in copper metabolism in a MT I/II mutant (MT-/-) fibroblast cell line (Tapia et al., 2004). We showed that MT-/- cells were more sensitive to increasing amounts of copper in the media than wild-type cells exposed to the same concentrations. Also, by measuring intracellular copper levels and by conducting uptake studies, we demonstrated that although both mutant and wild type cell lines accumulate copper upon treatment with copper, the MT-/- cells took up considerably less copper than the wild-type cells. Interestingly, in this condition, we observed that mutant cells died with lower intracellular copper content (2-fold lower), supporting a protective role for MT in the response to Cu excess. These results permitted us to deduce that copper toxicity does not rely on the increased amount of intracellular metal, but rather on the cellular ability to manage the metal, therefore, in the molecular interactions that copper establishes inside the cell. In this context, we showed that in the absence of MTs, the capacity of copper to induce gene expression of MT, SOD1 and its chaperone, Ccs, is lost. This observation could partially explain the increased vulnerability of MT null cells to lower intracellular copper concentrations and suggest that MT may be a modulator of gene expression (Tapia et al., 2004).

In the present study, we show that wild-type and mutant cells are undistinguishable in terms of their morphological features and rates of growth and define a minimal copper dose that provided a significant increment in the copper content of both cell lines. Using these conditions, we applied a genomic approach to further investigate a possible role of MTs as part of a pathway that induces gene expression in response to copper. As a first step in exploring the effects that loss of this important copper sequestering protein had on gene expression, we carried out microarray analysis to identify genes significantly up-regulated in wild-type and MT-/- cells exposed to an excess of copper and to determine which genes failed to be upregulated in MT mutant cells as compared to wild-type cells. The results of these analyses are presented here.


Cell lines and treatments

The cell lines used in the present study correspond to wild type and MT I/II mutant (MT-/-) fibroblasts obtained by trypsinization of mouse embryos from day 11 of gestation and immortalized with SV40 virus (Kelly and Palmiter, 1996). The mutation in the MT-/- cell line was achieved by introducing translation stop sequences in the MT I and II exons, thus the mutant cell line expresses a modified MT mRNA and fails to express the protein (Tapia et al., 2004). Culture and treatment conditions have been described (Tapia et al., 2004). Briefly, fibroblasts were incubated at 37 ºC in a 5% CO2 atmosphere and grown in plastic cell culture flasks (Nalge Nunc Int. Corp. IL, USA) containing Dulbecco's modification of Eagle's medium (DMEM) and 10% fetal bovine serum (SFB). The concentrations of elements in this basal culture medium were Cu 0.4, Fe 2.7 and Zn 3.8 μM (González et al., 1999). For all treatments, copper was supplemented in the cultured medium as Cu-His complex (1: 10 molar ratio) at the concentrations and times specified in the figure 2 legend. After the treatment, cells were processed for Cu, Zn and Fe quantification. To evaluate cell viability under copper treatment, cells were grown in 24-well cell culture plates (Nunc) and relative survival of the treated cells was evaluated using 3-[4,5-dimethylthiazol-2-yl]-2,5- diphenyltetrazolium bromide (MTT, Sigma) reduction assays as described (Denizot and Lang, 1986). The viability percentage was determined by comparing the measurements of the average absorbance from a given treatment group with that obtained from a reference sample of the same cell line treated for identical time with a control medium (100% of viability). To determine the population doubling time, the cell number was counted under a microscope daily for at least 5 days using a hemocytometer and the trypan blue (0.4%) exclusion method.

Immunofluorescence staining

Cells were washed three times with phosphate buffered saline (PBS), fixed for 10 min in 3.7% formaldehyde in PBS and permeabilized for 5 min with 0.2% triton X-100 in 3.7% formaldehyde. The fixed cells were re-hydrated with Tris buffered saline (TBS) and incubated for 1 h in blocking solution (3% BSA in TBS). To evidence the organization of microfilaments, cells were incubated with anti-actin monoclonal antibody (SIGMA) diluted 1: 500 in 3% BSA-TBS, and with the secondary antibody, FITC-conjugated rabbit-anti-mouse IgG (Rockland, Gilbertsville, PA), at a 1: 250 dilution in 3% BSA-TBS. Cells were incubated with primary or secondary antibodies for 1 h at 37°C. Finally, cells were rinsed in TBS, mounted in DABCO/mowiol, and examined with a epifluorescence microscope (40x objective, Nikon, Labophot-2, Tokyo, Japan). As controls, experiments were performed in which the first or second antibodies were omitted.

Cu, Fe and Zn quantification

For total metal content quantification, cells were processed as previously described (González et al., 1999; Tapia et al., 2004). Briefly, cells (2-4 x 105) at 80% of confluence were disrupted in concentrated suprapure nitric acid (Merck) in a vortex and diluted with distilled deionized water. Samples were digested at 60ºC overnight. The Cu determination was made by means of a graphite furnace atomic adsorption spectrophotometer (AAS, Perkin Elmer, SIMMA 6100). Calibration was against a standard curve made from dilutions of a Cu, Fe or Zn standard (J T Baker) and the sample values were normalized to the total protein content.

RNA isolation and cDNA labeling

Total RNA was extracted from wild-type and MT-/- mutant cell lines in the same passage number maintained under basal cell culture conditions or exposed to 100 mM Cu-His for 48 h using RNAWIZ reagent (Ambion). The indirect, or amino-allyl labeling protocol was adapted from the website ( // 25 μg total RNA and 5 μg of oligo dT were brought to a total volume of 15.5 μl and denatured for 10 min at 70ºC, then chilled on ice. An equal volume of reverse transcription reaction mix (2X first strand buffer, 20 mM DTT, 95 U SuperScript II, 1 mM dATP, 1 mM dGTP, 1 mM dCTP, 0.6 mM dTTP, and 0.4 mM amino-allyl-dUTP) was added, and the reaction was incubated at 42ºC overnight. The reaction was denatured by bringing it to 0.2 N NaOH, 0.1 M EDTA and incubating at 65ºC for 15 min, and neutralized by the addition of Tris-Cl pH 7.4 to a final concentration of 0.3 M. The buffer was removed, and the cDNA was concentrated by filtering through a Microcon-30. After drying in a speed vac, the cDNA was resuspended in 4.5 μl sterile water. The cDNA then was coupled to either monofunctional Cy3 or Cy5 dye (Amersham Pharmacia) in 0.1 M sodium bicarbonate buffer, pH 9.0, at room temperature, in the dark, for 1 h. The two dye reactions were purified separately with a Qia-Quick PCR purification kit (Qiagen). cDNA quantity and dye incorporation of each probe was assessed with a scanning spectrophotometer. The two dye probes were then combined and concentrated in a speed vac to a volume of 15-20 μl. SSC and SDS were added to a final concentration of 2.6X and 0.2% respectively. The probes were denatured for 2 min at 95ºC, allowed to cool, then placed on a post-processed microarray and incubated overnight at 60ºC. After hybridization, the microarray slides were washed at room temperature for 5 min in 1XSSC, and 0.05%SDS, then for 2 min in 0.2XSSC, and finally for 2 min in 0.1XSSC, and then were spin dried. The microarrays were fabricated at the College of Natural Resources Genomics Facility ( // These arrays contained 11,000 mouse cDNAs, randomly selected from the Brain Molecular Anatomy Project, BMAP ( // library (Research Genetics). Genes contained in this library are derived from 10 different adult mouse brain regions as well as spinal cord and retina.

Data analysis

Microarray slides were scanned on an ArrayWorx (Applied Precision) scanner. The intensity of hybridization values was determined using Genepix Pro 3.0 (Axon) image analysis software for each probe in both channels (Cy5- 695 nm, Cy3- 595 nm). All intensity values are background-subtracted, normalized by median of channel intensity (to account for dye bias), and log (base 2)- transformed. A recently developed method to identify differentially expressed genes between two mRNA samples, based on identification of outliers as candidate differentially expressed genes (Loguinov, et al., 2004), was used. The majority of data points after appropriate normalization lie in the vicinity of the line of equivalence in the scatter plot of log2(Cy5) vs. log2(Cy3) intensity values. Other data points, outliers, lie outside the vicinity of the line of equivalence and are considered to be data points of greatest interest, since they correspond to genes having noticeably different hybridization intensities. Robust scatter plot smoothers to quantify and take into account the distortion of the data set by heteroscedasticity (if any) were applied. Outliers from this analysis are considered to represent candidate differentially expressed genes. A confidence (p value) for each outlier is assigned by calculating simultaneous prediction confidence intervals (Loguinov et al., 2004). Sequence homology searches were done against mouse/rodent sequence databases, using the WU-BLAST 2.0 program at MouseBLAST ( // Differentially expressed genes were grouped according to their biological process using the Gene Ontology Classifications found at the Mouse Genome Informatics Website ( // and at the Gene Ontology Consortium Website ( //


The absence of MT does not modify the cellular morphology or the rate of growth of mutant fibroblasts

In order to assess whether the absence of MT affects the growth of mutant cells, the morphology and the rate of growth of both cell lines were compared. When wild-type and MT-/- cells were maintained in basal culture medium (0.4 μM Cu), they showed a monolayer growth pattern with similar sizes and morphological features (Fig. 1, upper panels), which is clearly observed by the organization of the microfilament network (Fig. 1, lower panels). After copper treatment, we did not detect changes in the morphological features of both cell lines (data not shown). In the absence of copper supplement, the growth curve of wild-type and MT-/- cells were nearly identical (Fig. 1). Once seeded, cells displayed a phase of slow growth (0-2 days) followed by of a phase of fast growth (3-5 days) until reaching confluence (>90% at day 5) at this time; their growth was inhibited by cellular contact. The deviation observed at day 5 was not statistically significant. From these curves, we calculated a population doubling time of 22 h. These results indicate that morphological features and proliferation rate of cells was unaffected by the absence of MT.


Figure 1. Comparison of morphological features and rate of growth between wild-type and MT-/- cells.
Microphotographs show the morphology of sub-confluent cultures of wild-type (A) and MT-/- (B) cells. Cells were analyzed using phase-contrast microscopy. Bar = 10 μm. Representative images of actin distribution patterns are shown for wild-type (C) and MT-/- (D). Microfilaments were stained as described in Materials and Methods. To determine the rate of growth, cells were cultured under basal conditions, and the total number of cells was quantified using trypan blue every day for 5 days. The experiment was performed in triplicate, and results are expressed as mean ± SD.


Differential Cu content and viability in wild type and MT-/- cells exposed to Cu-His

Wild-type and MT-/- cell lines growing in standard culture conditions showed no significant differences in the Cu, Fe and Zn content. When fibroblasts were exposed for 48 h with rising graded copper concentrations (up to 250 μM Cu-His), intracellular Cu content increased in both cell lines, but in wild-type fibroblasts, rose significantly more than in MT-/- fibroblasts (Fig. 2). Regarding the other trace metals, results show that Zn content remains unaffected and Fe content decreased about 2-fold in both cell lines. Thus, Cu exposure primarily affected intracellular Cu content, but also affected the Fe content to a lesser degree, providing further evidence for their metabolic interaction. Since we have shown that viability of wild-type and MT-/- cells exposed to an excess of Cu decreased in a time-dependent manner (Tapia et al., 2004), we selected a time of 48 hrs of copper-treatment for our gene expression analysis. The chosen extracellular copper concentration was 100 μM, a minimal dose of copper that generated a significant difference on intracellular Cu content between wild-type and MT-/- cells (Fig. 2). Under these conditions, cell viability of wild-type and MT-/- lines was 95.2% and 77.6%, respectively.

Figure 2. Cu, Fe and Zn content in wild-type and mutant MT-/- cells exposed to Cu-His.
Total metal content of wild-type cells and MT mutants determined by AAS in response to graded concentrations of Cu-His at 48 h. Filled bars correspond to wild-type cells and open bars to MT-/- cells. Each bar represents the mean value of triplicate experiments and corresponding standard deviation. ANOVA analysis for both cell types demonstrated a significant effect induced by Cu exposure. (*) denotes significant difference as compared to wild-type cells, p < 0.05; (**) denotes level of exposure in which the concentration effect was significant, p < 0.05.

Microarray experiment design

Gene expression in copper-treated wild type and MT-/- cells was compared to their untreated counterparts. RNA from four different cell conditions was used: 1) untreated wild-type cells; 2) 100 μM copper-treated wild-type cells; 3) untreated MT mutant cells; and 4) 100 μM copper-treated MT mutant cells. All copper-treated cells were treated for 48 hours prior to harvesting; the untreated cells were collected simultaneously. Wild-type was compared to copper-treated wild-type cells in four experiments; and MT-/- was compared to copper-treated MT-/- cells in four experiments. Although a total of eight microarray experiments were carried out, six were successfully completed and analyzed. Even though the repeated experiments were technical and not biological replicates, dye swaps were incorporated into some of them. The RNA used for each cell line was isolated on the same day; however, the microarray experiments (reverse transcription, labeling, and hybridizations) were done on different days.

Detection of differentially expressed genes

We identified differentially expressed genes from each hybridization using the outlier identification method described by Loguinov et al. (2004). We were interested in those genes, which were significantly upregulated in copper-treated cells (WT, 100 μM Cu and MT-/-, 100 μM Cu) as compared to untreated cells (WT and MT-/-). As shown in figure 3, the majority of the data points lie in the vicinity of a robust linear regression line of the scatter plot of log2(Cy5) v/s log2(Cy3) intensity values. These data points correspond to genes with similar hybridization intensity values in the two samples, while other data points lie outside the scatter plots and correspond to genes having noticeably different values of intensity. We determined Log2(Cy5/Cy3)/s(I) to estimate statistical significance (p values) for every gene to be a candidate for differential expression. s(I) is a robust scale estimator dependent on intensity and is used to build simultaneous prediction intervals for graphical representation of genes outside the intervals that are most likely outliers. Robust scatter plot smoothers are used to account for heteroscedasticity (variation in residual variance with intensity) in each data set. Red outliers on the top of the graph represent candidate up-regulated genes while the outlying spots of blue color, on the bottom, represent candidate down regulated genes. We considered data outliers with p-value 0.05 as candidate differentially expressed genes. We compared the candidate genes of each experiment and selected genes (i.e., outliers with a p-value < 0.05) identified in two or more repeat hybridizations as likely differentially expressed genes. In the WT, 100 μM Cu v/s WT experiments, there were 104 up-regulated genes in at least two of the three experiments, 31 of them were ESTs that had not yet been annotated. In the MT-/-, 100 μM Cu v/s MT-/- experiments there were 133 up-regulated genes, 37 of them corresponded to un-annotated genes. For each of the annotated genes, tables 1, 2 and 3 display the name, symbol and their GeneBank accession number. Genes upregulated in: a) both WT and MT -/- cells; b) only WT cells; and c) only MT -/- cells are listed in tables 1, 2 and 3, respectively.


Figure 3. Detection of differentially expressed genes.
Simultaneous prediction intervals (SPI) for the three WT,100 μM Cu v/s WT and the three MT-/-, 100 μM Cu v/s. MT-/- data sets (W1, W2 and W3 and M1, M2, and M3, respectively) are shown. For each experiment, the robust and resistant linear regression line (black) was calculated using the S-plus MM-estimator. Then the data was normalized by linear regression making slope = 1, intercept = 0 and subtracting the linear trend to deal with residuals that are log2(Cy5/Cy3). SPIs are corrected with the S-plus scatter plot smoother supsmu applied to absolute residuals, |log2(Cy5/Cy3)|, to reveal the dependence of residual variance on intensity values. The supsmu-based SPIs assume residual heteroscedasticity. Pink (cyan) points lie in the interval between the upper (lower) 90% and 95% SPIs. Red (blue) points lie above the upper (lower) 95% SPI. Black points lie below the upper and lower 90% SPI. The 90%, 95%, 99%, 99.9% and 99.99% SPIs are shown. The vertical dotted line marks the location of the minima of the empirical hyperbolas. Therefore, red/pink, blue/cyan and black points represent candidate upregulated, candidate downregulated and unchanged genes respectively.


Functional classification of differentially expressed genes

Functional annotation of the differentially expressed genes was performed aiming to discover features characteristic to the sets of genes up-regulated in 100 μM copper-treated WT and MT-/- cells. We classified genes from tables 1 and 2 according to their biological process using the GO database. GO provides a controlled vocabulary organized in a hierarchical fashion that can be applied to describe gene products from eukaryotic organisms regarding molecular function, biological process, and cellular component. GO terms for the biological process ontology were found for approximately 60% of the genes differentially expressed in 100 μM copper-treated WT and MT-/- cells. Pie graphs illustrating the biological process of genes up-regulated in 100 μM copper-treated WT and MT-/- cells are shown in figure 4A and B. Approximately 50% of the genes with known biological function are involved in cellular physiological processes. This group includes genes that play roles in signal transduction, transport, cytoskeleton organization, and regulation of transcription and translation. The next larger category (≈30%) corresponds to genes involved in metabolism. Within this category, 36% of the genes up-regulated in copper treated WT cells are involved in protein modification, whereas in copper-treated MT-/- cells the greatest percentage (36%) correspond to genes that play roles in protein biosynthesis. 15% of the genes up-regulated in copper-treated WT cells are involved in response to a stimulus (highlighted in grey, Tables 1 and 2), 75% of them correspond to genes with functions in stress response to temperature. In copper-treated MT-/- cells, there is a smaller portion of genes (9%) in this category (highlighted in grey, Tables 1 and 3), and only 25% of them correspond to those involved in response to temperature.


The role of MT has been extensively studied, however it remains elusive. Part of the reason is that MT has been implicated in a variety of physiological processes, such as metal storage, metal detoxification, oxidative scavenging, cell proliferation, and inflammatory response (Palmiter, 1998; Coyle et al., 2002).

In copper homeostasis, MT plays a role in the regulation of intracellular copper levels during adaptation to excess copper. It has been well demonstrated that MT protects cells against high levels of copper by sequestering excess amounts of the metal (Palmiter et al., 1992; Quaife et al., 1994; Haq et al., 2003). In addition to serving to detoxify excess copper, MT may play a role in normal copper metabolism. In a previous work (Tapia et al., 2004), we took advantage of the simultaneous generation of two fibroblast cell lines from littermate mouse fetuses (Kelly and Palmiter, 1996): one expresses MT, while the other expresses modified mRNA isoforms of MT I and II that are not able to be translated into proteins. In these cell lines, we evaluated the role of MT in Cu metabolism, monitoring a wide range of parameters such as viability, Cu content, Cu uptake and efflux, subcellular localization, and the expression of MT and some other Cu metabolism-related genes. Our results indicated that, within the physiological range, the role of MT is to provide a safe storage compartment for Cu. As a consequence of this function, at supra-physiological levels of Cu exposure MT has a role in detoxification. Additionally, MT is a modulator of gene expression, since in its absence, exposure to high Cu concentrations failed to induce the expression of MT and other Cu metabolism-related genes such as those encoding SOD1 and Ccs, suggesting a second mechanism by which MT may contribute to cellular resistance to Cu exposure.

In the present work, we further analyzed the effects that loss of MT had on gene expression using a genomic approach. In this study, we utilized cDNA microarray technology to evaluate the effects of copper excess on global gene expression in wild-type and MT-/- cells. In the microarray experiments, we compared transcripts from a wild-type to copper-treated wild-type cells, and from a MT-/- to copper-treated MT-/- cells. We were interested in determining genes that were upregulated in the two cell lines as a result of handling excess of copper and identifying which genes failed to be upregulated in MT null cells as compared to wild-type cells. We hypothesized that, by comparing the effects of copper overload in a normal cell to copper overload in a Mt deficient cell, insight into MT's normal role in copper homeostasis could be gained. We were interested in the differences/similarities in the handling of excess copper between the two cell types to understand what pathways are affected only in the MT deficient cells, as this might indicate areas where MT is required. Any similarities in affected pathways would likely indicate areas where MT is not important or uninvolved.

It is generally accepted that copper in excess, due to its redox cycling capacity, can give rise to the generation of reactive oxygen species capable of producing oxidative stress (Halliwell and Gutteridge, 1984) and that MT protects the cell from this oxidative stress by sequestering excess copper (Dameron and Harrison, 1998; Kaway et al., 2000). Thus, we expected that stress would be high in MT-/- cells exposed to excess levels of copper. When we analyzed the genes up-regulated in 100 mM copper-treated wild-type cells, we found that seven genes encoding heat shock proteins were induced. These heat shock proteins _ Hspb1, Hspca, Hsp105, Hspa1a, Hspa8, Dnajb6, and Dnajc10 _ are widely conserved and over-expressed at high temperatures or other stress conditions (Lindquist and Craig, 1988). Moreover, catalase (cat) and superoxide dismutase 3 (Sod3) were also upregulated in the 100 μM copper-treated cells, as compared to untreated wild-type cells. Induction of these genes generally indicates that the cell is undergoing stress (Whitley et al., 1999; Nollen and Morimoto, 2002; Bauer and Bauer, 2002; Otterbein et al., 2003). Surprisingly, only three of the stress-related genes (Hspa1a, Dnaja1, and Hspd1) were induced in 100 μM copper-treated MT-/- cells, indicating that the MT-/- cells are not responding with induction of typical markers of cellular stress under copper excess conditions, as compared to the wild-type cell line. In a previous work, using the same experimental approach, we utilized fibroblast cell lines from two mutant mice, C57BL/6-Atp7a (Mobr) and C57BL/6-Atp7a (Modap), to evaluate the effects of chronic copper overload on cellular gene expression (Armendáriz et al., 2004). These cells showed a severe loss-of-function in the ATP7a gene with a cellular defect in copper efflux that leads to high levels of intracellular copper accumulation in standard culture media. Similar results to those obtained in MT-/- cells exposed to copper were observed for both ATP7a mutant cell lines, showing no differential expression of oxidative stress genes, besides the up-regulation of MT. When taken together, these results suggest that the transcriptional regulation of stress genes is affected when the machinery that controls copper homeostasis is altered. It is possible that: 1) the cells are unable to sense stress; or 2) the untreated MT-/- cells are already stressed, thus explaining why there is no difference as compared to copper loaded MT-/- cells.

Figure 4. Functional classifications of up-regulated genes.
Up-regulated genes in 100 μM copper-treated WT (A) and MT-/- cells (B) with known functions were grouped according to their biological process in three major categories: Cellular physiological process, Metabolism, and Response to stimulus. Subcategories are labeled a to r.



Genes commonly up-regulated in 100 mM copper-treated WT and
MT-/- cells (p-value < 0.05)

GenBank Gene name Symbol


adenomatosis polyposis coli Apc


capping protein, alpha 2 Capza2
AI839184 DNA segment, Chr 3, MJeffers 1


AI839363 eukaryotic translation initiation factor 3, subunit 6



eukaryotic translation initiation factor 5 Eif5
AI841289 heat shock protein 1A Hspa1a

heterogeneous nuclear ribonucleoprotein A2/B1

AI850620 matrin 3


AI480893 metallothionein 2


AI846930 progesterone receptor membrane component 1


AI843656 protein kinase C, delta


AI838689 protein tyrosine phosphatase 4a2



RAB7, member RAS oncogene family

AI845039 RIKEN cDNA 1110038O08 gene


AI839993 scavenger receptor class B, member 2


AI840197 secreted acidic cysteine rich glycoprotein Sparc
AI841699 ubiquitin A-52 residue ribosomal protein fusion product 1


AI836012 t-complex-associated-testis-expressed 1-like


AI838607 thrombospondin 1


AI847817 tight junction protein 1


AI836699 zinc finger, A20 domain containing 2 Za20d2



Genes up-regulated in 100 μM copper-treated WT cells (p-value < 0.05)


Gene name Symbol


5'-3' exoribonuclease 2 Xrn2
AI839327 activating transcription factor 7 interacting protein



advanced glycosylation end product-specific receptor

AI838490 amyloid beta (A4) precursor-like protein 1


AI854771 angiomotin Amot
AI849453 arginyl-tRNA synthetase Rars


ATPase type 13A2 [Mus musculus] Atp13a2
AI844698 ATP-binding cassette, sub-family A, member 2 (Abca2)


AI527414 catalase Cat
AI835756 dendritic cell protein GA17


AI836002 DNA segment, Chr 13, Wayne State University 64, expressed


AI842025 DNA segment, Chr 5, Brigham & Women's Genetics 0860 expressed


AI845673 DnaJ (Hsp40) homolog, subfamily B, member 6 Dnajb6
AI838060 DnaJ (Hsp40) homolog, subfamily C, member 10 Dnajc10


erythrocyte protein band 4.1-like 2 Epb4.1l2


ferritin heavy chain Fth


Growth hormone inducible transmembrane protein Ghitm


heat shock protein 1 Hspb1
AI836122 heat shock protein 1, alpha Hspca
AI838486 heat shock protein 105 Hsp105
AI841358 heat shock protein 8 Hspa8


hemochromatosis Hfe


heterogeneous nuclear ribonucleoprotein A3 Hnrpa3
AI836554 high density lipoprotein-binding protein Hdlbp
AI851942 kelch repeat and BTB (POZ) domain containing 2 Kbtbd2


kinesin family member 5B Kif5b


leukocyte receptor cluster, member 5 Leng5
AI839417 moesin Msn


myosin, light polypeptide 9, regulatory Myl9


platelet-activating factor acetylhydrolase, isoform 1b, beta1 subunit Pafah1b1


proteolipid protein Plp


RAB10, member RAS oncogene family Rab10


Rap2 interacting protein Rap2ip


RIKEN cDNA 1700064K09 gene 1700064K09Rik


IKEN cDNA 2210401K01 gene R2210401K01Rik


RIKEN cDNA 2310037P21 gene 2310037P21Rik
AI845633 RIKEN cDNA 6130401J04 gene 6130401J04Rik


RIKEN cDNA A430005L14 gene A430005L14Rik
AI851553 RIKEN cDNA E430034L04 gene E430034L04Rik


ring finger protein 13 Rnf13


SET translocation Set


olute carrier family 37 (glycerol-3-phosphate transporter), member 3 sSlc37a3


superoxide dismutase 3, extracellular Sod3
AI834833 transducin (beta)-like 1X-linked receptor 1 Tbl1xr1


transformed mouse 3T3 cell double minute 2 Mdm2
AI848382 ubiquitin specific protease 1 Usp1


vesicular inhibitory amino acid transporter Viaat


zinc finger, CCHC domain containing 6 Zcchc6



Genes up-regulated in 100 μM copper-treated MT-/- cells (p-value < 0.05)

Gene name Symbol
annexin A5 Anxa5
ATP synthase, H+ transporting, mitochondrial F0 complex,b, isoform 1 Atp5f1
AI848681 ATPase, H+ transporting, lysosomal accessory protein 2 Atp6ap2
AI836191 ATP-binding cassette, sub-family C, member 5


AI848245 beta-2 microglobulin


AI854022 carnitine deficiency-associated gene expressed in ventricle Cdv3
AI847251 casein kinase 1, alpha 1 Csnk1a1
AI845078 CDC42 small effector 1 Cdc42se1
AI844682 cell division cycle 42 homolog (S. cerevisiae) Cdc42
AI841451 cut-like 1 (Drosophila)



death-associated kinase 3 Dapk3
AI841974 DNA segment, Chr 11, ERATO Doi 99, expressed D11Ertd99e


DnaJ (Hsp40) homolog, subfamily A, member 1 Dnaja1


enhancer of polycomb homolog 1 (Drosophila) Epc1


eukaryotic translation elongation factor 1 alpha 1 Eef1a1


eukaryotic translation initiation factor 2, subunit 2 (beta) Eif2s2


eukaryotic translation initiation factor 4, gamma 2 Eif4g2
AI841804 expressed in non-metastatic cells 1 Nme1
AI847926 golgi apparatus protein 1 Glg1
AI838039 heat shock protein 1 (chaperonin)


AI841981 hepatitis B virus x interacting protein


AI843558 heterogeneous nuclear ribonucleoprotein K



heterogeneous nuclear ribonucleoprotein U Hnrpu
AI836129 high mobility group nucleosomal binding domain 2 Hmgn2
AI850268 methionine adenosyltransferase II, alpha


AI853257 mitochondrial ribosomal protein S33


AI853143 mortality factor 4 like 1


AI847934 neurofilament, light polypeptide


AI848144 neuron specific gene family member 2


AI841664 nucleosome assembly protein 1-like 1 Nap1l1
AI838078 nudix-type motif 9 Nudt9
AI852884 Phosphatidylinositol binding clathrin assembly protein


AI848346 polyadenylate-binding protein-interacting protein 2 Paip2
AI843948 proteasome subunit, alpha type Psma3,
AI838874 protein phosphatase 2a, catalytic subunit, beta



GenBank Gene name Symbol

AI838463 RAS related protein 1b Rap1b
AI849041 Ras-like without CAAX 2 Rit2
AI847923 regulator of G-protein signaling 2 Rgs2
AI844168 reticulon 4 receptor Rtn4r

ribonuclease P 40 subunit (human)

AI851588 ribosomal protein L23 Rpl23
AI834863 ribosomal protein L26 Rpl26

ribosomal protein S3a


RIKEN cDNA 1110055L24 gene

AI847909 RIKEN cDNA 1700030A21 gene 1700030A21Rik

RIKEN cDNA 2210409B22 gene


RIKEN cDNA 2310047D13 gene


RIKEN cDNA 2410002O22 gene


RIKEN cDNA 3110001N18 gene


RIKEN cDNA 4631403P03 gene

AI843449 RIKEN cDNA 4921531G14 gene G630041M05Rik

RIKEN cDNA 5730454B08 gene


RIKEN cDNA 5730470L24 gene


RIKEN cDNA 7530403E16 gene


RIKEN cDNA 8430420C20 gene


RIKEN cDNA A730042J05 gene

AI853842 RWD domain containing 1 Rwdd1

SECIS binding protein 2

AI847805 secreted phosphoprotein 1 Spp1

SMT3 suppressor of mif two 3 homolog 1 (yeast)

AI845086 smu-1 suppressor of mec-8 and unc-52 homolog (C. elegans) Smu-1

spectrin beta 2


spectrin beta 3

AI843287 Tax1 binding protein 1 Tax1bp1



transcription factor 4


transducin (beta)-like 3


transforming growth factor beta 1 induced transcript 4


tumor differentially expressed 2


tumor protein D52

AI845961 ubiquitin-conjugating enzyme E2L 3 Ube2l3,



  N-acetylgalactosaminyltransferase 10




It is relatively well established that MT-deficient cells are more sensitive (i.e., less viable) to excess copper; therefore, it seems counterintuitive that these cells did not show signs of increased stress. However, it is important to note that these MT-/- cells were shown by us (Tapia et al., 2004) to accumulate less copper when exposed to increasing levels of the metal. A similar phenomenon was seen in MT-deficient cells exposed to lead. In this study, lead-exposed cells were more sensitive to lead despite accumulating much less of the metal as compared to their wild-type counterparts (Qu et al., 2002). This might suggest that MT-/- cells are unable to sense the stress, and perhaps it is the lack of induction of the stress response pathways that make them more sensitive to these metals. This potential incapability to sense the stress might be related to impaired activation of the MTF-1 transcription factor, since the specific activation of MTF-1 requires, in addition to copper excess, a zinc-saturated MT (Zhang et al., 2003). MTF-1 is involved in several cellular responses, including oxidative stress, hypoxia, and amino acid starvation (Murphy et al., 1999), and its activation might be modulated by heat shock (Saydam et al., 2003), which place MTF-1 as an important component of the cross-talk between different anti-stress systems in the cell. The possibility that untreated MT-/- cells are already stressed is consistent with their higher sensitivity to copper exposure as compared to wild-type cells, which has been observed in cell viability studies by us and others (Kelly and Palmiter, 1996; Tapia, 2004) and with the fact that in the absence of MT, cells are unable to store copper in a safe compartment (Tapia et al., 2004). In this scenario, we might assume a high level of expression of stress genes, even when cells are exposed to low extracellular copper. Therefore, we are unable to detect significant changes in the relative expression of stress genes; in order to clarify this point, it is necessary to perform a comparison between untreated wild-type and MT-/- cells. Moreover, we cannot rule out the option that the mechanisms to induce the expression of stress genes in MT-/- cells require a longer period of time to become activated, thus it

will be interesting to perform serial time-course microarray experiments to compare the gene profile in wild-type and MT-/- cell lines.

Among other genes up-regulated in 100 μM copper-treated wild-type cells, we found ferritin, an iron sequestering protein composed of 2 types of subunits _ H (heavy chain) and L (light chain) _ that play a key role in the maintenance of the intracellular iron balance (Torti and Torti, 2002). Although ferritin is known primarily for its critical role in cellular and organism iron homeostasis, it is unlikely that high iron levels are inducing ferritin, as intracellular iron levels in both the MT-/- and WT cells slightly decrease upon copper treatment (Fig. 2). There is evidence, however, that suggests that ferritin plays a role in protection against oxidative damage (Arosio and Levi, 2002). It has been shown that overexpression of the H subunit leads to a reduced production of reactive oxygen species (ROS) after exposure to hydrogen peroxide and that ferritin is subject to both transcriptional, as well as translational, regulation by oxidative stress (Tsuji et al., 2000; Orino et al., 2001). Further studies will be needed to understand the role of MT in the transcriptional regulation of ferritin in copper overload cells.

Another gene with potential roles in metal homeostasis is HFE, the hemochromatosis gene. Mutations in this gene cause progressive body iron overload, which leads to tissue damage and ultimately multiorgan failure (Drakesmith and Townsend, 2000; Parkkila et al., 2001). The function of HFE protein is unknown, but some evidence suggests that it acts together with beta2-microglobulin and transferrin receptor 1 to regulate iron uptake in the intestinal cells (Anderson and Powell, 2002). In the Caco2 cell line, it was shown that HFE mRNA is induced by Fe, but not by other metals (Co, Cu, and Zn) (Han et al., 1999), and there is currently no evidence to suggest that it is induced by oxidative stress (Sánchez et al., 1998; Mura et al., 2004). As with ferritin, further studies are necessary to understand the significance of HFE induction in the copper-treated cells.

A large proportion of genes (>80%) upregulated in wild-type and MT-/- cells after copper exposure were classified into two major categories: 1) metabolism; and 2) cellular physiological processes. A similar distribution was reported by Armendáriz et al. (2004) for the two cell lines that accumulate copper due to a defect in copper export, suggesting that copper overload induces the expression of genes associated with diverse molecular function. Therefore, microarray analysis seems to be useful to compare the behavior of wild-type cells and cells with mutations in different components of Cu metabolism in response to fluctuations in Cu availability. We consider that the results obtained through these experiments provide experimental support to connect copper homeostasis with other metabolic pathways.


This work was supported by grants 1050235 and 1030618 from Fondecyt (to VC and MG) and by grants from the International Copper Association, United States Department of Agriculture NRI 9900815 and a University of California Toxic Substance (to CDV) Research and Training Program traineeship (ADA).


ANDERSON GJ, POWELL LW (2002) HFE and non-HFE hemochromatosis. Int J Hematol. 76: 203-207         [ Links ]

ARMENDÁRIZ AD, GONZÁLEZ M, LOGUINOV AV, VULPE CD (2004) Gene expression profiling in chronic copper overload reveals upregulation of Prnp and App. Physiol Genomics. 20: 45-54         [ Links ]

AROSIO P, LEVI S (2002) Ferritin, iron homeostasis, and oxidative damage. Free Radic Biol Med. 33: 457-463         [ Links ]

BAUER M, BAUER I (2002) Heme oxygenase-1: Redox regulation and role in the hepatic response to oxidative stress. Antioxid Redox Signal. 4: 749-758         [ Links ]

BREMNER I, BEATTIE JH (1990) Metallothionein and the trace minerals. Annu Rev Nutr. 10: 63-83         [ Links ]

COUSINS RJ (1983) Metallothionein — Aspects related to copper and zinc metabolism. J Inherit Metab Dis. 6 Suppl 1: 15-21         [ Links ]

COYLE P, PHILCOX JC, CAREY LC, ROFE AM (2002) Metallothionein: The multipurpose protein. Cell Mol Life Sci. 59: 627-647         [ Links ]

DAMERON CT, HARRISON MD (1998) Mechanisms for protection against copper toxicity. Am J Clin Nutr. 67 5 Suppl: 1091S-1097S         [ Links ]DENIZOT F, LANG R (1986) Rapid colorimetric assay for cell growth and survival. Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability. J. Immunol. Methods. 89: 271-277         [ Links ]

DRAKESMITH H, TOWNSEND A (2000) The structure and function of HFE. Bioessays. 22: 595-598         [ Links ]

FREEDMAN JH, PEISACH J (1989) Resistance of cultured hepatoma cells to copper toxicity. Purification and characterization of the hepatoma metallothionein. Biochem Biophys Acta. 992: 145-154         [ Links ]

GONZÁLEZ M, TAPIA L, ALVARADO M, TORNERO JD, FERNÁNDEZ, R (1999) Intracellular determination of trace elements by total-reflection X-ray fluorescence spectrometry in mammalian cultured cells. J Anal At Spectrom. 14: 885-888         [ Links ]

HALLIWELL B, GUTTERIDGE JM (1984) Oxygen toxicity, oxygen radicals, transition metals and disease. Biochem J. 219: 1-14         [ Links ]

HAN O, FLEET JC, WOOD RJ (1999) Reciprocal regulation of HFE and NNamp2 gene expression by iron in human intestinal cells. J Nutr. 129: 98-104         [ Links ]

HAQ F, MAHONEY M, KOROPATNICK J (2003) Signaling events for metallothionein induction. Mutat Res. 533: 211-226         [ Links ]

KAWAI K, LIU SX, TYURIN VA, TYURINA YY, BORISENKO GG, JIANG JF, ST CROIX CM, FABISIAK JP, PITT BR, KAGAN VE (2000) Antioxidant and antiapoptotic function of metallothioneins in HL-60 cells challenged with copper nitrilotriacetate. Chem Res Toxicol. 13: 1275-1286         [ Links ]

KELLY EJ, PALMITER RD (1996) A murine model of Menkes disease reveals a physiological function of metallothionein. Nat Genet. 13: 219-222         [ Links ]

KELLY EJ, QUAIFE CJ, FROELICK GJ, PALMITER RD (1996) Metallothionein I and II protect against zinc deficiency and zinc toxicity in mice. J Nutr. 126: 1782-1790         [ Links ]

KLAASSEN CD, LIU J (1998) Metallothionein transgenic and knock-out mouse models in the study of cadmium toxicity. J Toxicol Sci. 23 Suppl 2: 97-102         [ Links ]

LEONARD SS, BOWER JJ, SHI X (2004) Metal-induced toxicity, carcinogenesis, mechanisms and cellular responses. Mol Cell Biochem. 255: 3-10         [ Links ]

LINDQUIST S, CRAIG E (1988) The heat-shock proteins. Annu. Rev. Genet. 22: 631- 677         [ Links ]

LIU J, LIU Y, HARTLEY D, KLAASSEN CD, SHEHIN-JOHNSON SE, LUCAS A, COHEN SD (1999) Metallothionein-I/II knockout mice are sensitive to acetaminopheninduced hepatotoxicity. J Pharmacol Exp Ther. 289: 580-586         [ Links ]

LIU Y, LIU J, HABEEBU SM, WAALKES MP, KLAASSEN CD (2000) Metallothionein- I/II null mice are sensitive to chronic oral cadmium-induced nephrotoxicity. Toxicol Sci. 57: 167-176         [ Links ]

LOGUINOV AV, MIAN IS, VULPE CD (2004) Exploratory differential gene expression analysis in microarray experiments with no or limited replication. Genome Biol. 5: R18         [ Links ]

MURA C, LE GAC G, JACOLOT S, FEREC C (2004) Transcriptional regulation of the human HFE gene indicates high liver expression and erythropoiesis coregulation. Faseb J. 18: 1922-1924         [ Links ]

MURPHY BJ, ANDREWS GK, BITTEL D, DISCHER DJ, MCCUE J, GREEN CJ, YANOVSKY M, GIACCIA A, SUTHERLAND RM, LADEROUTE KR, WEBSTER KA (1999) Activation of metallothionein gene expression by hypoxia involves metal response elements and metal transcription factor-1. Cancer Res. 59: 1315-1322         [ Links ]

NOLLEN EA, MORIMOTO RI (2002) Chaperoning signaling pathways: molecular chaperones as stress-sensing `heat shock' proteins. J Cell Sci. 115: 2809-2816         [ Links ]

NORDBERG GF (1989) Modulation of metal toxicity by metallothionein. Biol Trace Elem Res. 21: 131-135         [ Links ]

ORINO K, LEHMAN L, TSUJI Y, AYAKI H, TORTI SV, TORTI FM (2001) Ferritin and the response to oxidative stress. Biochem J. 357: 241-247         [ Links ]

OTEÍZA PI, MACKENZIE GG, VERSTRAETEN SV (2004) Metals in neurodegeneration: Involvement of oxidants and oxidant-sensitive transcription factors. Mol Aspects Med. 25: 103-115         [ Links ]

OTTERBEIN LE, SOARES MP, YAMASHITA K, BACH FH (2003) Heme oxygenase: unleashing the protective properties of heme. Trends Immunol. 24: 449-455         [ Links ]

PALMITER RD, FINDLEY SD, WHITMORE TE, DURNAM DM (1992) MT-III, a brainspecific member of the metallothionein gene family. Proc Natl Acad Sci U S A. 89: 6333-6337         [ Links ]

PALMITER RD (1998) The elusive function of metallothioneins. Proc Natl Acad Sci U S A. 95: 8428-8430         [ Links ]

PARK JD, LIU Y, KLAASSEN CD (2001) Protective effect of metallothionein against the toxicity of cadmium and other metals. Toxicology. 163: 93-100         [ Links ]

PARKKILA S, NIEMELA O, BRITTON RS, FLEMING RE, WAHEED A, BACON BR, SLY WS (2001) Molecular aspects of iron absorption and HFE expression. Gastroenterology. 121: 1489-1496         [ Links ]

PETRIS MJ, MERCER JF, CULVENOR JG, LOCKHART P, GLEESON PA, CAMAKARIS J (1996) Ligand-regulated transport of the Menkes copper P-type ATPase efflux pump from the Golgi apparatus to the plasma membrane: A novel mechanism of regulated trafficking. Embo J. 15: 6084-6095         [ Links ]

PULIDO MD, PARRISH AR (2003) Metal-induced apoptosis: Mechanisms. Mutat Res. 533: 227-241         [ Links ]

QU W, DIWAN BA, LIU J, GOYER RA, DAWSON T, HORTON JL, CHERIAN MG, WAALKES MP (2002) The metallothionein-null phenotype is associated with heightened sensitivity to lead toxicity and an inability to form inclusion bodies. Am J Pathol. 160: 1047-1056         [ Links ]

QUAIFE CJ, FINDLEY SD, ERICKSON JC, FROELICK GJ, KELLY EJ, ZAMBROWICZ BP, PALMITER RD (1994) Induction of a new metallothionein isoform (MT-IV) occurs during differentiation of stratified squamous epithelia. Biochemistry. 33: 7250-7259         [ Links ]ROJAS P, KLAASSEN CD (1999) Metallothionein-I and -II knock-out mice are not more sensitive than control mice to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine neurotoxicity. Neurosci Lett. 273: 113-116         [ Links ]

SÁNCHEZ M, QUERALT R, BRUGUERA M, RODES J, OLIVA R (1998) Cloning, sequencing and characterization of the rat hereditary hemochromatosis promoter: comparison of the human, mouse and rat HFE promoter regions. Gene. 225: 77-87         [ Links ]

SAYDAM N, STEINER F, GEORGIEV O, SCHAFFNER W (2003) Heat and heavy metal stress synergize to mediate transcriptional hyperactivation by metal-responsive transcription factor MTF-1. J Biol Chem. 278: 31879-31883         [ Links ]

TAPIA L, GONZÁLEZ-AGÜERO M, CISTERNAS MF, SUAZO M, CAMBIAZO V, UAUY R, GONZÁLEZ M (2004) Metallothionein is crucial for safe intracellular copper storage and cell survival at normal and supra-physiological exposure levels. Biochem J. 378(Pt 2): 617-624         [ Links ]

THEOCHARIS SE, MARGELI AP, KOUTSELINIS A (2003) Metallothionein: A multifunctional protein from toxicity to cancer. Int J Biol Markers. 18: 162-169         [ Links ]

TORTI, FM TORTI SV (2002) Regulation of ferritin genes and protein. Blood. 99: 3505-3516         [ Links ]

TSUJI Y, AYAKI H, WHITMAN SP, MORROW CS, TORTI SV, TORTI, FM (2000) Coordinate transcriptional and translational regulation of ferritin in response to oxidative stress. Mol Cell Biol. 20: 5818-5827         [ Links ]

UAUY R, OLIVARES M, GONZÁLEZ M (1999) Essentiality of copper in humans. Am J Clin Nutr. 67: 952S-959S         [ Links ]

WHITLEY D, GOLDBERG SP, JORDAN WD (1999) Heat shock proteins: A review of the molecular chaperones. J Vasc Surg. 29: 748-751         [ Links ]

ZHANG B, GEORGIEV O, HAGMANN M, GUNES C, CRAMER M, FALLER P, VASAK M, SCHAFFNER W (2003) Activity of metal-responsive transcription factor 1 by toxic heavy metals and H2O2 in vitro is modulated by metallothionein. Mol Cell Biol. 23: 8471-8845         [ Links ]

ZHENG H, LIU J, LIU Y, KLAASSEN CD (1996) Hepatocytes from metallothionein-I and II knock-out mice are sensitive to cadmium- and tert-butylhydroperoxide-induced cytotoxicity. Toxicol Lett. 87: 139-145         [ Links ]

Corresponding author: Mauricio González, Laboratorio de Bioinformática y Expresión Génica, INTA, Universidad de Chile, Macul 5540, Macul, Santiago, Chile, Tel.: (56-2) 978-1440, Fax: 56-2-221-4030, E-mail:

Received: February 15, 2005. Accepted June, 25 2005.



Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons