J Biol Chem, Vol. 274, Issue 34, 24142-24146, August 20, 1999

Transferrin Receptor Induction by Hypoxia
HIF-1-MEDIATED TRANSCRIPTIONAL ACTIVATION AND CELL-SPECIFIC POST-TRANSCRIPTIONAL REGULATION^*

Lorenza Tacchini, Laura Bianchi, Aldo Bernelli-Zazzera, and Gaetano Cairo^§

From the Istituto di Patologia Generale, Università di Milano e Centro di Studio sulla Patologia Cellulare, Consiglio Nazionale delle Ricerche, via Mangiagalli 31, 20133 Milano, Italy

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

The tight relationship between oxygen and iron prompted us to investigate whether the expression of transferrin receptor (TfR), which mediates cellular iron uptake, is regulated by hypoxia. In Hep3B human hepatoma cells incubated in 1% O₂ or treated with CoCl₂, which mimics hypoxia, we detected a 3-fold increase of TfR mRNA despite a decrease of iron regulatory proteins activity. Increased expression resulted from a 4-fold stimulation of the nuclear transcription rate of the TfR gene by both hypoxia and CoCl₂. A role for hypoxia-inducible factor (HIF-1), which activates transcription by binding to hypoxia-responsive elements in the activation of TfR, stems from the following observations. (a) Hypoxia and CoCl₂-dependent expression of luciferase reporter gene in transiently transfected Hep3B cells was mediated by a fragment of the human TfR promoter containing a putative hypoxia-responsive element sequence, (b) mutation of this sequence prevented hypoxic stimulation of luciferase activity, (c) binding to this sequence of HIF-1, identified by competition experiments and supershift assays, was induced in Hep3B cells by hypoxia and CoCl₂. In erythroid K562 cells, the same treatments did not affect iron regulatory proteins activity, thus resulting in a stimulation of TfR gene expression higher than in hepatoma cells.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Iron is needed for several essential functions but is also potentially dangerous as a catalyst of reactive oxygen species production (1). Thus, iron is usually bound to proteins, and iron homeostasis is tightly regulated. Iron in serum is mainly transported by transferrin (Tf),¹ which delivers the metal to cells requiring it. Iron-laden Tf interacts with transferrin receptor (TfR), and the complex is then internalized by receptor-mediated endocytosis. Since the TfR plays a crucial role in the control of iron entry into cells, its expression is tightly regulated. Iron controls TfR mRNA levels through a well characterized post-transcriptional mechanism involving binding of cytosolic iron regulatory proteins (IRPs) to iron-responsive elements (IREs) in the 3'-untranslated region of TfR mRNA (2, 3). In conditions of iron depletion, IRP actively binds to IREs and increases TfR mRNA stability by preventing access to ribonucleases (2, 3). Since, at the same time, the IRE-IRP interaction prevents ferritin mRNA translation, the combined effect of this regulation results in increased iron availability in the intracellular pool. An inverse regulation occurs when iron is plentiful in such a way that iron homeostasis is maintained. On the other hand, iron-independent TfR expression is mainly controlled at the transcriptional level (4). Indeed, elevated transcription is an important means to provide high TfR expression in erythroid (5) and mitogen-activated (6, 7) cells.

Hypoxia is increasingly recognized as an important regulator of gene expression, and a number of physiologically relevant genes have been found to be induced by hypoxic conditions that may help the cell to adapt to reduced oxygen supply (8-11). Although post-transcriptional mechanisms may contribute to the induction of hypoxia-sensitive genes, hypoxia-inducible factor (HIF-1), which activates gene transcription in response to reduced oxygen concentration, is the most relevant component of the molecular response to hypoxia. HIF-1 is a heterodimer consisting of an  and  subunit; the latter is identical to the aryl hydrocarbon receptor nuclear translocator (ARNT), which is also able to dimerize with the aryl hydrocarbon receptor. Hypoxia results in the stabilization of HIF-1, enabling it, upon dimerization with the constitutively expressed ARNT and formation of a complex with the transcriptional coactivator p300/CBP, to bind hypoxia-responsive elements (HREs) in responsive genes.

Hypoxia stimulates erythropoiesis and intestinal iron absorption (12), and it is therefore conceivable that proteins involved in iron transport and uptake are regulated by oxygen supply. Indeed, serum Tf levels increase in animals exposed to hypoxia (13), and it has been recently shown that Tf gene expression is induced by hypoxia in hepatoma cells (14). However, for efficient erythropoiesis, transferrin must be iron-loaded and internalized through interaction of Tf with TfR, and hence, the increased plasma iron transport capacity provided by hypoxic up-regulation of Tf expression (14) should be followed by increased availability of cellular Tf binding sites.

Here we show that TfR gene transcription is stimulated by hypoxia and that a HIF-1 binding site in the TfR promoter is involved in this response. Cell-specific modulation of IRP activity, by allegedly regulating TfR mRNA stability, possibly represents an additional level of control.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Cell Lines and Culture Conditions-- Hep3B hepatoma cells were grown in minimal essential medium and K562 human erythroleukemia cells in RPMI 1640. Media were supplemented with 10% heat-inactivated fetal calf serum, 2 mM L-glutamine, 100 units/ml penicillin, 0.1 mg/ml streptomycin. Cell lines were maintained in a humidified incubator at 37 °C in 5% CO₂, 95% air. For hypoxic stimulation, cells at 90% confluency were placed in an incubator chamber that was thoroughly flushed with a gas mixture containing 5% CO₂, 1% O₂ and nitrogen-balanced, tightly sealed, and incubated at 37 °C for different time periods as described (15). The pH of the culture medium did not change after 20 h of hypoxia. Cells were also exposed to 100 µM CoCl₂ or 100 µM desferrioxamine (Sigma) for different time periods.

Northern Blot Analysis-- Total cellular RNA was isolated as described (16), and equal amounts of RNA were electrophoresed under denaturing conditions. To confirm that each lane contained equal amounts of total RNA, the ribosomal RNA content in each lane was estimated in the ethidium bromide-stained gels by laser densitometry. RNA was transferred to Hybond-N filters (Amersham Pharmacia Biotech), which were hybridized with ³²P-labeled human TfR cDNA pTR10 (17). Quantitative determination was achieved by direct nuclear counting using an InstantImager (Packard Instruments Co.), and the values were calculated after normalization to the amount of ribosomal RNA.

Nuclear Transcription Assay-- Nuclei were purified and incubated for in vitro transcription as described (18). ³²P-Labeled nuclear RNA elongated in vitro was purified, and equal amounts of trichloroacetic acid-precipitable radioactivity for each sample were hybridized to the following DNA probes fixed on nitrocellulose filters: human heme oxygenase (HO-1) (19), L-ferritin subunit (20), and TfR (17) cDNAs. Hybridization signals were evaluated by direct nuclear counting using an InstantImager and normalized to the values of L-ferritin subunit after subtraction of the background values represented by the hybridization signals of the empty plasmid pGEM (Promega, Milano, Italy).

In Vitro RNA Transcription-- The pSPT-fer plasmid containing the iron-responsive element of human ferritin H chain (21) was linearized with BamHI and transcribed in vitro with T7 RNA polymerase in the presence of 100 µCi of [-³²P]UTP (800 Ci/mmol, Amersham Pharmacia Biotech).

RNA-Protein Gel Retardation Assay-- Cells were homogenized in the buffer described by Leibold and Munro (22), the lysate was centrifuged at 16,000 × g, and the supernatant was used for an RNA-protein band shift assay. Samples containing 2 µg of protein (determined using the Bio-Rad protein assay kit) were incubated in the absence or presence of 2% 2-mercaptoethanol, with a molar excess of IRE probe. Incubation, digestion with RNase T1, and treatment with heparin were performed as previously described (23). After separation on 6% nondenaturing polyacrylamide gels, RNA-protein complexes were visualized by autoradiography and quantitated by direct nuclear counting using an InstantImager.

Plasmid Constructs-- To construct the pTfRA-luc vector, a 1710-bp EcoRI-EcoRV fragment excised from plasmid pAT153-E5.E5 (24) was filled and inserted into the SmaI site of the pGL2 vector (Promega, Milano, Italy). To obtain the pTfRB-luc clone, a 455-bp fragment was amplified from the No. 9 derivative of plasmid pcD-TR1 (25) using oligonucleotides corresponding to positions -439 to -424 and +2 to +16 as 5' and 3' primers, respectively. The amplified product was blunted and inserted into the SmaI site of the pGL2 vector (Promega, Milano, Italy). Mutation of the putative HRE sequence 5'-TACGTGC-3' centered at position -86 in the sense DNA strand of the pTfRB-luc plasmid with replacement of the bases TACGT with AATTC to construct pTfRBm-luc was introduced by polymerase chain reaction-based site-directed mutagenesis using the ExSite mutagenesis kit (Stratagene, Milano, Italy). All constructs were verified by DNA sequencing.

Transient Transfection Assay-- Subconfluent Hep3B cells were transiently cotransfected using the calcium phosphate method with 10 µg of a 50:1 mixture of pGL2 constructions and pRL-SV40 reporter vector containing Renilla luciferase, which was used to normalize for transfection efficiency. After recovering for 48 h, the cells were subjected to the various treatments. Cells were collected, washed, and lysed using the reporter lysis buffer (Promega, Milano, Italy). Luciferase activities were then measured in a Lumat LB 9501 luminometer (Berthold) using the dual-luciferase reporter assay system (Promega, Milano, Italy) according to the manufacturer's instructions.

Nuclear Extract and Electrophoretic Mobility Shift Assay-- The HRE sequence was synthesized to match W18 in Wang and Semenza (26). The TfR-18 oligonucleotide corresponding to sequences from nucleotide position -93 to -75 relative to the transcription start site in the human TfR gene (AGCGTACGTGCCTCAGGA) was labeled with [-³²P]ATP by means of T4 polynucleotide kinase. Hep3B nuclear extract (10 µg of protein) prepared as described (26) was preincubated in 10 mM Tris, pH 7.8, 50 mM NaCl, 1 mM EDTA, 5% (v/v) glycerol, 5 mM dithiothreitol, and 20 µg/ml poly(dI·dC) for 5 min at room temperature before the addition of 0.5 ng of labeled probe. For supershift assay, 1 µg of OZ15 monoclonal antibody to HIF-1 (NeoMarkers, Union City, CA) was added, and the binding reaction mixture was incubated at 4 °C for 90 min. After 20 min at room temperature, reaction products were electrophoresed at 4 °C in 5% polyacrylamide in 30 mM Tris, 30 mM boric acid, 0.06 mM EDTA.

	RESULTS

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Analysis of TfR mRNA Levels-- TfR expression in response to hypoxia was studied in a line of hepatoma cells that is extensively used to investigate regulation of genes associated to hypoxic stress. Northern blot analysis (Fig. 1) showed that incubation of Hep3B cells in reduced oxygen atmosphere (1% O₂) for 20 h strongly increased TfR mRNA steady state levels. Quantification of four experiments showed a 3-fold induction. Treatment with CoCl₂, a well known inducer of several hypoxia-responsive genes (8-11), also increased TfR mRNA expression to a similar extent.

View larger version (102K): [in this window] [in a new window]   Fig. 1.   Northern blot analysis of TfR mRNA levels. A filter with equal amounts of total cellular RNA, as revealed by ethidium bromide fluorescence of ribosomal RNAs, was hybridized with the TfR cDNA as indicated under "Experimental Procedures." RNA was isolated from Hep3B cells left untreated (lane 1), maintained under hypoxia for 20 h (lane 2), or treated with 100 µM CoCl2 for 20 h (lane 3). The autoradiogram shown is representative of four independent experiments.

Bandshift Assay of IRP Activity-- Since TfR is known to be regulated at post-transcriptional level by the IRE-IRP interaction (2, 3), we investigated the IRE binding activity of IRP by RNA bandshift assays in cytosolic extracts of Hep3B cells. Fig. 2 demonstrates that IRP activity in human hepatoma cells was up-regulated by iron chelation, as expected on the basis of previous work (2, 3), and markedly repressed (70% inactivation, as revealed by quantification of three separate experiments) by both hypoxic exposure and treatment with CoCl₂ for 20 h, as previously shown for rat hepatoma cells (27). Treatment of cell extracts with 2-mercaptoethanol, which fully activates latent IRP (2, 3), eliminated all the differences, thus indicating equal loading of all samples and suggesting that inactivation was due to a post-translational switch. Experiments with murine cells in which, at a difference from human cells, separation and detection of IRP-1 versus IRP-2 by bandshift assays is possible, demonstrated that the two IRPs are divergently regulated by hypoxia (27, 28). We cannot specify the role of the two IRP isoforms in hypoxic human hepatoma cells; nevertheless, as IRP-1 and IRP-2 bind IREs with similar affinity and specificity (2, 3, 29), a decrease of TfR mRNA stability should reflect the observed reduction of total IRP binding activity.

View larger version (102K): [in this window] [in a new window]   Fig. 2.   Bandshift assay of IRP activity. Cytoplasmic lysates were incubated with an excess of 32P-labeled IRE probe in the presence or absence of 2% 2-mercaptoethanol (2ME), which is known to activate IRP binding activity. RNA-protein complexes were separated on nondenaturing 6% polyacrylamide gels and revealed by autoradiography. Extracts were prepared from Hep3B cells left untreated (lane 1), treated with 100 µM desferrioxamine for 20 h (lane 2), maintained under hypoxia for 20 h (lane 3), or treated with 100 µM CoCl2 for 20 h (lane 4). The autoradiogram shown is representative of three independent experiments.

Run-on Transcription Analysis-- The increase of TfR mRNA levels in the presence of reduced IRP activity pointed to a transcriptional effect on TfR expression. To directly assess this aspect, we measured TfR gene transcription in isolated nuclei. Fig. 3 shows that the transcription rate of TfR gene is stimulated by both hypoxia and CoCl₂ with a response similar to that of the heme oxygenase gene, which has been shown to be transcriptionally activated by hypoxia (30). On the other hand, transcription of the gene for ferritin L subunit was not altered by these treatments. Quantification of three separate experiments showed a 4-fold induction of TfR gene transcription.

View larger version (36K): [in this window] [in a new window]   Fig. 3.   Nuclear run on assay of TfR transcription. Equal amounts of 32P-labeled RNA synthesized in vitro by isolated nuclei purified from Hep3B cells left untreated (C), maintained under hypoxia for 12 h, or treated with 100 µM CoCl2 for 12 h were hybridized to panels of the indicated DNA probes (pGEM, pGemini; L, ferritin L subunit; HO, heme oxygenase; TfR, transferrin receptor) immobilized on nitrocellulose filters. The autoradiogram shown is typical of three different experiments.

Transcriptional Activity of the TfR Promoter-- We then analyzed the structure of the TfR gene to determine whether any consensus HREs were present that might account for our observations of hypoxic induction of TfR gene transcription. Search for potential binding sites in the promoter region extending 1.7 kilobases upstream of the initiation site with the MatInspector V2.2 program revealed two binding sites matching the consensus for AHR/ARNT (NGCGTGA/C) and two binding sites for HIF-1/ARNT (TACGTGC), one on the sense and another on the antisense strand. To further clarify the role of transcriptional activation in hypoxia-mediated TfR gene expression, a 1710-bp fragment of the human TfR promoter region was cloned in front of luciferase, and the resulting construct (pTfRA-luc) was transiently transfected in Hep3B cells (Fig. 4A). As indicated by previous evidence showing that less than 200 bp of 5' region are sufficient for expression of the TfR gene (24), the cloned fragment was sufficient for efficient transcription of the promoterless reporter gene in transfected normoxic cells, as demonstrated by a several hundred-fold induction of basal luciferase activity over that of the empty pGL2 Basic vector. Exposure to hypoxia for 20 h stimulated luciferase expression 2.5-fold, as revealed by quantification of 3 experiments (Fig. 4B). Treatment with CoCl₂ induced a slightly stronger response. No elevation was observed after a similar induction of cells transfected with the control pGL2 DNA. To better define the promoter region that confers oxygen responsiveness to TfR, we focused on a shorter region containing the sequence 90 to 83 relative to the transcription start site on the sense strand (5'-TACGTGC-3'), which matches consensus HREs and that is positioned 15 bases upstream of a CACA repeat, which seems to be necessary for hypoxic inducibility (8). A 455-bp fragment (pTfRB-luc) was used for transfection and reporter gene assays, and its activity was compared with that of a similar construct (pTfRBm-luc) in which the HRE sequence on the sense strand had been mutated (Fig. 4A). This shorter fragment conserved high basal transcription efficiency and was still able to confer hypoxic inducibility of luciferase activity to an extent similar to that previously observed with the longer construct (Fig. 4B). In agreement with the observation that the HIF-1/HRE interaction is important for basal transcription levels of hypoxia-inducible genes also under normoxic conditions (31), the mutation somewhat decreased the basal levels of pTfRBm-luc reporter activity (data not shown), but importantly, also prevented almost completely the hypoxia-stimulated increase of luciferase activity (Fig. 4B), thus suggesting that this sequence is a functional HRE in the response of TfR to hypoxia.

View larger version (33K): [in this window] [in a new window]   Fig. 4.   Reporter gene activation assay of TfR transcription. Panel A, structures of reporter gene constructs. A 1710- or 455-bp fragment derived from the TfR promoter (pTfRA-luc and pTfRB-luc, respectively) was cloned in front of the firefly luciferase gene. The expansion shows a sequence containing the putative HRE with the core motif in boldface (pTfRB-luc). This sequence was mutated in pTfRBm-luc (underlined). Panel B, transient expression assay. Hep3B cells were cotransfected with reporter plasmids and control vector pRL-SV40, which contains the Renilla luciferase gene. After exposure of transfected cells to normoxia (20% O2), hypoxia (1% O2), or CoCl2 for 20 h, luciferase activity was determined, corrected for transfection efficiency according to the Renilla luciferase activity, and normalized to the normoxic relative luciferase activity arbitrarily defined as 1. All values represent mean ± S.D. of at least four independent experiments.

DNA Binding Activity to the TfR HRE-- To assess whether the sequence found in the TfR gene promoter with high homology to consensus HRE was the target of HIF-1, nuclear extracts were analyzed by electrophoretic mobility shift assays. Fig. 5, panel A shows that the TfR-18 probe detected a constitutively expressed DNA binding activity (C) as well as a DNA binding activity (HIF-1) present in hypoxic and CoCl₂-treated cells (lanes 2 and 3) and absent in nonhypoxic cells (lane 1). The specificity of the interaction between the probe and hypoxia-induced factors was tested by competition with nonradioactive oligonucleotides. Inclusion of increasing amounts of unlabeled TfR-18 oligonucleotides (lanes 4-6) inhibited the binding of the constitutive and inducible complexes. Competition with cold oligonucleotides corresponding to the HRE present in the erythropoietin enhancer (W-18, lanes 7-9) suggested that the hypoxia-inducible factor binding the TfR probe was indeed HIF-1. To further determine the composition of the hypoxia and CoCl₂-induced complexes, nuclear extracts were incubated with a monoclonal antibody to HIF-1 before the mobility shift assay. Supershift assays (Fig. 5, panel B, lanes 3 and 4) showed that HIF-1 interacts with the HRE sequence of the TfR gene.

View larger version (46K): [in this window] [in a new window]   Fig. 5.   Analysis of HIF-1 DNA binding activity. Panel A, mobility shift assay. Nuclear extracts prepared from Hep3B cells left untreated (lane 1), maintained under hypoxia for 4 h (lanes 2 and 4-9), or treated with 100 µM CoCl2 for 4 h (lane 3) were incubated with radioactive TfR-18 in the absence (lanes 1-3) or presence of increasing amounts (100-, 200-, 400-fold molar excess) of unlabeled TfR-18 (lanes 4-6) and W-18 (lanes 7-9) oligonucleotides. Position of complexes containing constitutive (C) or HIF-1 binding activity is indicated. Panel B, supershift assay. DNA binding activities of nuclear extracts prepared from Hep3B cells maintained under hypoxia for 4 h (lanes 1 and 3) or treated with 100 µM CoCl2 for 4 h (lanes 2 and 4) were assayed as described above in the absence (lanes 1 and 2) or presence (lanes 3 and 4) of OZ15 monoclonal antibody against HIF-1. Positions of the supershift complexes (S) is indicated. The autoradiograms shown in both panels A and B are representative of at least four different experiments.

TfR Gene Expression in Erythroid Cells-- Erythroid cells rely almost completely on transferrin-bound iron for hemoglobin synthesis and therefore express TfR at high levels (5). Thus, to investigate whether hypoxic stimulation of TfR expression was extended to erythroid cells, we subjected K562 cells to hypoxic and CoCl₂ treatment. Northern blot analysis demonstrated a marked up-regulation of the TfR transcript not only in desferrioxamine-treated K562 cells, as expected, but also in hypoxic and CoCl₂-treated cells, (Fig. 6, panel A). Indeed, quantification of three different experiments showed that TfR gene expression was stimulated 8-fold in hypoxic versus normoxic cells, i.e. to a greater extent than in hepatoma cells (see Fig. 1). Interestingly, RNA bandshift assays (Fig. 6, panel B) demonstrated that in erythroid cells, IRP activity was stimulated by desferrioxamine but not affected by hypoxia. These findings suggest therefore that in these cells the increased transcription of TfR gene was not counteracted by the decreased mRNA stability, which should be the result of down-regulation of IRP activity, thus resulting in higher accumulation of TfR mRNA.

View larger version (60K): [in this window] [in a new window]   Fig. 6.   Regulation of TfR expression in erythroid cells. Panel A, a filter with equal amounts of total cellular RNA, as revealed by ethidium bromide fluorescence of ribosomal RNAs, was hybridized with the TfR cDNA as indicated in the legend to Fig. 1. RNA was isolated from K562 cells normoxic (lane 1), treated with 100 µM desferrioxamine (lane 2), hypoxic (lane 3), or treated with 100 µM CoCl2 (lane 4). The autoradiogram shown is representative of three independent experiments. Panel B, cytoplasmic lysates from K562 cells normoxic (lane 1) treated with desferrioxamine 100 µM (lane 2), hypoxic (lane 3), or with 100 µM CoCl2 (lane 4) were incubated with an excess of 32P-labeled IRE probe in the presence or absence of 2% 2-mercaptoethanol. RNA-protein complexes were separated on nondenaturing 6% polyacrylamide gels and revealed by autoradiography. The autoradiogram shown is representative of three independent experiments.

	DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Results reported in the present paper add TfR to the growing list of hypoxia-inducible genes and thus strengthen the link between iron metabolism and oxygen homeostasis. In fact, all the major genes of iron metabolism respond to hypoxia. Although IRP-1 and IRP-2 modulation under hypoxic conditions is determined at a post-translational level (27, 28), and ferritin induction is post-transcriptionally controlled as a result of IRP inactivation (32, 33), the expression of Tf (14) and TfR (present study) is transcriptionally regulated. It is evident that there is post-transcriptional regulation of TfR expression via IRP-mediated control of mRNA stability in response to iron (2, 3) and other stimuli (34, 35); however, we provide here results from several lines of investigation to show that hypoxic stimulation of TfR expression is mainly transcriptional. Indeed, run-on experiments demonstrated elevated transcription of the TfR gene in hypoxic and CoCl₂-treated cells, which resulted in a rise of steady-state mRNA levels. Transfection experiments provided further evidence for the critical role of transcriptional control in the response of TfR expression to reduced oxygen concentration. We also demonstrated that hypoxia stimulates TfR gene transcription through HIF-1, the best characterized transcriptional activator of hypoxia-sensitive genes. Indeed, a well conserved HRE sequence is present in the human TfR promoter; moreover, when cells were transfected with constructs in which the putative HRE was mutated to abolish HIF-1 binding, inducibility by hypoxia was lost. Results of supershift assays are also consistent with HIF-1 acting as a transactivating factor in the response of TfR to hypoxia. Indication that the TfR HRE is necessary to confer transcription activation in response to hypoxia and that TfR possesses the main properties shared by HIF-1-regulated genes (11) is provided by two other types of evidence. (i) The extent of response was similar when luciferase expression was driven by both the 1.7-kilobase- and the 455-bp-long promoters, thus indicating that the latter contained the main regulatory element(s), and (ii) mutation of the HRE around 85 almost completely abolished the response to reduced oxygen concentration, thus indicating the absence of other critical sites within the shorter construct. The present results suggest that in Hep3B cells, transcriptional induction was sufficient to overcome the counteracting effect of decreased IRP activity, which, on the basis of the well known effects of the IRE-IRP interaction on TfR mRNA turnover (2, 3), is expected to have decreased TfR mRNA stability.

While this study was in preparation, it was reported that the activation of IRP binding capacity induced by hypoxia in Hep3B cells resulted in higher expression of TfR and suppression of ferritin synthesis (36). We have no immediate explanation for the discrepancy between our results, which are in agreement with previous evidence of a reduced IRP-1 binding in murine hepatoma cells and macrophages (27, 28, 32), and those of Toth et al. (36). However, with regard to the post-transcriptional control imposed by IRPs, since the two IRPs are regulated oppositely by hypoxia (28) i.e. decreased IRP-1 and increased IRP-2 activity, the discrepancy in the observed total IRP activity (IRP-1 and IRP-2) may depend on the relative abundance of the two forms in a particular cell. In turn, this can be influenced by a variety of parameters, such as iron content of the medium and proliferative status of the cell (37), which could possibly account for the divergent results obtained in different laboratories using the same cell line. On the other hand, although increased total IRP activity as the result of higher IRP-2 levels is plausible in cells rich in IRP-2, e.g. 293 human kidney cells (28), a similar up-regulation is less likely in Hep3B cells, where the amount of IRP-2 is low (36).

Although hepatoma cells are a convenient system to study hypoxia, the dependence of liver cells on Tf iron is limited. Indeed, hepatic TfR expression is immediately down-regulated by iron overload in patients with hemochromatosis (38) who nonetheless accumulate iron from non-transferrin sources (39). On the other hand, erythroid cells use almost exclusively Tf-bound iron for proliferation and hemoglobin synthesis. It is therefore of interest that in these cells, which are exquisitely sensitive to changes in oxygen supply, hypoxic response of TfR is not only maintained but is even increased compared with that of hepatoma cells. The large accumulation of TfR mRNA is possibly the result of the combination of elevated transcription and unaltered mRNA stability, as inferred on the basis of previous work (2, 3) by the lack of changes of IRP activity, although the contribution of a higher transcription rate cannot be excluded.

Increased RNA stability is an additional mechanism for the induction of hypoxia-inducible genes (9). The results presented here suggest that hypoxia modulates TfR expression at multiple levels in a cell-specific way. Unidirectional activation, through increased transcription and unchanged, IRP-mediated, mRNA stability (discussed above), occurs in erythroid cells, whereas in hepatic cells the two controls are divergent, and reduced IRP activity counteracts in part enhanced transcription, eventually resulting in a smaller rise of TfR mRNA. One can speculate whether this cell-specific response is aimed at providing bone marrow cells with plenty of iron for eythropoiesis while preventing excessive entry of the metal into other cells where free iron could trigger formation of reactive oxygen species during reoxygenation or post-ischemic reperfusion.

	ACKNOWLEDGEMENTS

We thank L. Kuhn for the generous gift of the pSPT-fer, pAT153-E5.E5, and pcD-TR1 plasmids, D. Fornasari for help with the determination of luciferase activity, M. Minuzzo for K562 cells, B. Giglioni for the pGL2 vector, and A. Rossi for technical assistance.

	FOOTNOTES

^* This work was supported by grants from Consiglio Nazionale delle Ricerche (CNR) and Ministero dell'Università e della Ricerca Scientifica e Tecnologica (MURST).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

These authors contributed equally to the work.

^§ To whom correspondence should be addressed: Istituto Patologia Generale, Università di Milano, Via Mangiagalli 31, 20133 Milano, Italy. Tel: 390270630821; Fax: 390226681092; E-mail: gaetano.cairo@unimi.it.

	ABBREVIATIONS

The abbreviations used are: Tf, transferrin; TfR, Tf receptor; IRP, iron regulatory protein; IRE, iron-responsive element; ARNT, aryl hydrocarbon receptor nuclear translocator; HRE, hypoxia-responsive element; bp, base pair(s).

	REFERENCES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES