|Home | About | Journals | Submit | Contact Us | Français|
Nucleotide duplications in exon 4 of the ferritin light polypeptide (FTL) gene cause the autosomal dominant neurodegenerative disease neuroferritinopathy or hereditary ferritinopathy (HF). Pathologic examination of patients with HF has shown abnormal ferritin and iron accumulation in neurons and glia in the central nervous system (CNS) as well as in cells of other organ systems, including skin fibroblasts. To gain some understanding on the molecular basis of HF, we characterized iron metabolism in primary cultures of human skin fibroblasts from an individual with the FTL c.497_498dupTC mutation.
Compared to normal controls, HF fibroblasts showed abnormal iron metabolism consisting of increased levels of ferritin polypeptides, divalent metal transporter 1, basal iron content and reactive oxygen species, and decreased levels of transferrin receptor-1 and IRE-IRP binding activity.
Our data indicates that HF fibroblasts replicate the abnormal iron metabolism observed in the CNS of patients with HF. We propose that HF fibroblasts are a unique cellular model in which to study the role of abnormal iron metabolism in the pathogenesis of HF without artifacts derived from over-expression or lack of endogenous translational regulatory elements.
Abnormal brain iron metabolism leading to neurodegeneration is the main feature of diseases such as Friedreich ataxia (FRDA), aceruloplasminemia, neurodegeneration with brain iron accumulation type I (NBIA I), and hereditary ferritinopathy (HF) or neuroferritinopathy [1-3]. HF is an adult-onset autosomal dominant disease caused by nucleotide duplications in exon 4 of the ferritin light polypeptide (FTL) gene. Six different mutations have been reported, leading to an increase in the length and a change of the amino acid sequence of the C-terminus of FTL [4-9]. HF affects the central nervous system (CNS) presenting clinically as an extra-pyramidal movement disorder accompanied by cognitive and behavioral disturbances, starting between the third and sixth decade of life . Neuropathologically, HF is characterized by a severe neuronal loss in the basal ganglia, atrophy of cerebellum and cerebral cortex, abnormal iron accumulation, and the presence of ferritin inclusion bodies (IBs) in neurons and glia . Ferritin IBs are not limited to the CNS since they can also be seen in hepatocytes, cells of the renal tubular epithelium, endothelial cells of capillaries, and skin fibroblasts [5,6].
Ferritin is the main intracellular iron storage protein, having a central role in the regulation of cellular iron metabolism and iron detoxification [11,12]. Mammalian ferritin consists of 24 subunits of FTLs and ferritin heavy polypeptides (FTH); the FTH subunit is involved in the rapid detoxification of iron, whereas the FTL subunit facilitates iron nucleation, mineralization, and long-term iron storage . Ferritin provides both a source of metabolic active iron and also serves as an oxygen free radical cytoprotective protein, storing iron that is not needed for immediate metabolic use [11,12]. Each subunit consists of a bundle of 4 parallel α-helices (A, B, C, and D), a long extended loop (connecting helices B and C), and a C-terminus with a short α-helix (E) which is involved in important stabilizing interactions around the 4-fold symmetry axes . Spectroscopic and biochemical studies of recombinant mutant FTL homopolymers assembled from the p.Phe167SerfsX26 polypeptide (originated from the c.497_498dupTC mutation)  have shown that the mutation causes conformational changes in ferritin, altering iron incorporation and promoting iron-mediated aggregation of ferritin. The process of iron-induced aggregation of ferritin does not seem to involve covalent bonds since it can be reversed by iron-chelants both in vitro and in vivo . X-ray crystallographic analysis of homopolymers of the mutant p.Phe167SerfsX26 polypeptide showed the complete absence of the E helical domain of FTL in mutant subunits and substantial disruption of the 4-fold pores of the 24-mer . Transgenic expression of the p.Phe167SerfsX26 polypeptide in mice recapitulated several features of the disease, including intracellular formation of ferritin IBs in neurons and glia in the CNS and in cells of other organ systems, including skin fibroblasts . Transgenic mice showed dysregulation of iron homeostasis and evidence of oxidative damage in the brain, similarly to what has been observed in individuals with HF . Herein, we report ferritin accumulation, iron dyshomeostasis and evidence of oxidative stress in human skin fibroblasts from a patient with HF. Our results reveal that the broad dysfunction of iron homeostasis observed in individuals with HF and in the transgenic animal model of HF is replicated in HF skin fibroblasts. We propose that HF skin fibroblasts represent a unique cellular model in which to study the molecular mechanisms of cellular toxicity that may lead to neurodegeneration in HF.
Confocal fluorescence microscopy analysis (Figure (Figure1)1) using abs against the mutant-FTL chain showed that the mutant polypeptide accumulated both in the cytoplasm and in the nucleus of HF fibroblasts (Figure (Figure1e),1e), as previously reported in skin fibroblasts of individuals with HF and transgenic mice [5,16]. No staining was observed in normal control skin fibroblasts (non-HF) (Figure (Figure1b).1b). Western blot analysis showed expression of the ferritin subunits in normal and in HF fibroblasts (Figure (Figure2a).2a). Antibodies against the N-terminus of FTL detected two bands on western blots of HF fibroblasts, in agreement with the difference in molecular weight between wild-type and mutant-FTL polypeptides . Densitometric analysis showed a statistically significant (p < 0.05) increase in the levels of ferritin light and heavy polypeptides in HF fibroblasts (FTH1: 3.2 fold; FTL: 4.7 fold) (Figure (Figure2b2b).
Western blot analysis of the expression of TfR1 and DMT1 + and - IRE isoforms (+/-IRE-DMT1) showed significant changes in the levels of both proteins (Figure 3a, b). Densitometric analysis showed a statistically significant (p < 0.05) decrease in the levels of TfR1 (reaching a level of 70 ± 11% of non-HF control) and a statistically significant (p < 0.05) increase in the total levels of the iron influx transporter +/-IRE-DMT1 (118 ± 10% of non-HF control), mainly in bands corresponding to molecular weights of ~70 kDa and ~50 kDa. No significant changes were observed for FPN (Figure 3c, f).
Total iron contents were measured using a ferrozine-based iron assay . Mutant fibroblasts showed a statistically significant (p < 0.05) increase in the levels of basal iron content when compared to non-HF fibroblasts (non-HF: 10.9 ± 1.2 nmol Fe/mg protein; HF: 13.6 ± 1.4 nmol Fe/mg protein) (Figure (Figure4a).4a). LIP, the iron available for metabolism processes in the cell, was measured using a modified calcein assay [19-21]. No statistically significant differences in the levels of LIP were observed under basal conditions (BC) between HF and non-HF fibroblasts. LIP levels in normal and HF fibroblasts increased with statistical significance upon exposure to 100 μM FAC (Figure (Figure4b4b).
Under basal conditions, IRE-IRP binding was found to be reduced in HF fibroblasts when compared to normal fibroblasts (non-HF: 100 ± 12%; HF: 88 ± 8%) (Figure (Figure5).5). When fibroblasts where subjected to FAC treatment for 72 h, a significant decrease in IRE-IRP binding was observed in HF and non-HF fibroblasts. Interestingly, the change in IRE-IRP binding after treatment with FAC was more pronounced in HF fibroblasts than in control fibroblasts (non-HF: 60 ± 7%; HF: 24 ± 9%) (Figure (Figure5b).5b). After 2-ME treatment to promote maximal IRE-IRP1 binding [22,23], IRP binding activity increased nearly to 100%, suggesting that the majority of the observed decreased in binding activity may be associated with binding of IRP1 rather than IRP2 [22,23].
ROS formation in cultured fibroblasts was determined using the fluorescent dye 2',7'-dichlorodihydrofluorescein under basal conditions and after treatment with FAC. Under basal conditions, HF fibroblasts showed significant higher levels of ROS than non-HF fibroblasts (Figure (Figure6).6). A statistically significant increase in cellular oxidant levels was observed in normal and HF fibroblasts after loading with FAC for 72 h. Interestingly, ROS levels were significantly higher in HF fibroblasts compared to non-HF fibroblasts after FAC treatment.
The neurodegenerative disease neuroferritinopathy or HF is an autosomal dominant, adult onset disease caused by mutations in the FTL gene that lead to the production of FTL polypeptides with abnormal C-termini [3-9,24]. The clinical presentation of HF varies both within and between families. Patients may present with tremor, cerebellar signs, parkinsonism, psychiatric problems, abnormal involuntary movements (dystonia, chorea), pyramidal syndrome, pseudo-bulbar symptoms, and cognitive deficit [3-10]. Magnetic resonance imaging shows abnormal signals in the globus pallidus and putamen, and cavitation in the putamen [5,10]. Mild cerebral and cerebellar atrophy may be observed. Serum ferritin levels may be within normal range or even decreased in some patients . Neuropathologic studies show cavitation in the putamen [4-6]. The cerebrum and cerebellum are atrophic. Ferritin IBs are found in nuclei and cytoplasm of glial cells and neurons in the CNS as well as in cells of other organ systems and are labeled by antibodies against light and heavy chains of ferritin and antibodies specific for the mutant FTL polypeptide . Abnormal iron accumulation (both as ferrous and ferric iron) associated with ferritin IBs has been described [4-6] as well as evidence of oxidative damage in patients  and in animal models [17,25]. Thus, disrupted iron homeostasis and iron-mediated oxidative stress may have a major role in the pathogenesis of HF [3,24].
We investigated cellular iron metabolism in primary cell cultures of skin fibroblasts from an individual with the c.497_498dupTC mutation to determine whether fibroblasts would be an accessible in vitro system in which to directly examine disease-relevant pathologic mechanisms in HF. Our results clearly show alterations of iron metabolism in HF fibroblasts, which seem to recapitulate the abnormalities seen in HF patients and transgenic mice [5,6,16,17]. Ferritin is considered a cytoplasmic iron-storage protein; however, a nuclear localization for ferritin  has been described in animal models of iron overload , and in avian  and human astrocytoma cells . In HF fibroblasts, we observed ferritin accumulation in the nucleus and cytoplasm of the cells under basal conditions, as reported in cells from patients affected by HF  and in transgenic mice over-expressing mutant FTL . Ferritin accumulation may be explained by the formation of ferritin aggregates and/or by overproduction of ferritin (enhanced transcription/translation of ferritin mRNAs) by the cells in response to a diminished iron-binding activity of mutation-containing ferritin. We have previously shown that ferritin containing the mutant FTL polypeptide has a diminished ability to sequester and store mineralized iron in vitro [14,15,30] and does not lead to an increase in the transcription of ferritin polypeptide genes in vivo in mice, although transgenic mice accumulate ferritin as intracytoplasmic and intranuclear IBs [16,17]. Thus, we proposed that the mutant FTL polypeptide may act in vivo as a dominant negative mutant, causing the failure of ferritin in its iron storage function and leading to an increase in the levels of intracellular iron and the translation of ferritin mRNAs (Figure (Figure7)7) . In HF fibroblasts, we observed an increase in protein levels of ferritin polypeptides and a decrease in the protein levels of TfR1. Proteins of iron metabolism are known to be regulated in a coordinated fashion mainly at the post-transcriptional level . IRPs when interacting with IRE at the 5' -untranslated regions (UTR) of FTH1 and FTL mRNA inhibit their translation, whereas the interaction between IRPs with the IREs located at the 3' UTR of TfR1 mRNA stabilizes the mRNA, increasing TfR1 protein levels . Thus, the finding of increased protein levels of FTL and FTH and a decrease in TfR1 protein levels in concert with a decrease in the binding activity of IRP-IRE in HF fibroblasts strongly supports the notion of a failure of ferritin in its iron storage function in HF fibroblasts, leading to an increase in FTL and FTH1 translation and degradation of TfR1 mRNA. As would be expected, treatment with FAC of normal and HF fibroblasts leads to a significant decrease in IRE-IRP binding in both cases. However, the change in IRE-IRP binding after treatment with FAC was more pronounced in HF fibroblasts than in control fibroblasts, suggesting a lower IRE-IRP binding activity and consequent translation of ferritin mRNA and destabilization of TfR1 mRNA in HF fibroblasts. In agreement with the data obtained in transgenic mice, no significant changes in the protein levels of the iron exporter FPN were observed . We detected an increase in the protein levels of DMT1 (+/-IRE) in HF fibroblasts, which may account for the increase in total iron observed in HF fibroblasts. DMT1, a proton-coupled metal transporter that participates in iron influx to the cell from the extracellular matrix and/or from recycling endosomes  has been shown to contribute to the neurodegenerative process occurring in Parkinson disease (PD), where an increase in the expression of DMT1 (+IRE) in the sustancia nigra of patients with PD correlates with an increase in iron content .
The expression profile of iron related-proteins and the IRE-IRP binding activity in HF fibroblasts suggest that the cells might be exposed to elevated levels of intracellular iron. Indeed, we observed that the total cellular iron levels were increased in HF fibroblasts compared to wild-type fibroblasts under basal conditions, although no statistically significant differences between control and HF fibroblast were observed in the levels of the iron available for metabolic processes in the cell (or LIP) under basal conditions. LIP in quiescent conditions represents only a minor fraction of the total cell iron and can undergo dynamic changes in response to various treatments , as seen when HF and non-HF fibroblasts were challenged with iron. The observed response of LIP to iron treatment suggests differential management of free intracellular iron in HF fibroblasts. HF fibroblasts showed increased ROS production compared to non-HF fibroblasts, which is in agreement with the finding of an increase in iron levels in HF fibroblasts under basal conditions. Iron imbalance and augmented cellular sensitivity to oxidative damage has also been observed in HeLa cells over-expressing the mutant ferritin c.460dupA or the c.497_498dupTC . These data are consistent with studies in transgenic mice, which showed increased iron levels, lipid peroxidation, protein carbonylation, and nitrone products in the CNS , and the biochemical and immunohistochemical evidence for oxidative damage, lipid peroxidation and abnormal protein nitration observed in individuals with HF .
The abnormally high iron levels observed in several neurodegenerative disorders have been proposed to lead to oxidative stress and neurodegeneration [17,36-39]. In HF, we found that a defect in a protein of iron metabolism leads to neurodegeneration, directly connecting abnormal iron metabolism and neurodegeneration (Figure (Figure7).7). Our findings suggest that HF fibroblasts recapitulate the abnormal iron metabolism seen in patients with HF and in a transgenic animal model of HF. Further studies using the HF fibroblast cell model will provide additional insights into the mechanism(s) by which dysfunction of iron homeostasis may lead to neurodegeneration. In addition, they may be important in the characterization of therapeutic agents for HF and related diseases.
Dulbecco's Minimal Essential Medium (DMEM) 4.5 g/L glucose, fetal bovine serum (FBS), L-glutamine, penicillin/streptomycin, trypsin-EDTA solution and phosphate buffered saline (PBS) were obtained from Invitrogen (Carlsbad, CA). All cell culture plastics were obtained from Nunc (Rochester, NY, USA). All other general laboratory chemicals were obtained from Sigma-Aldrich Corp. (St. Louis, MO), unless specified.
Adult skin fibroblasts were isolated from an individual with the c.497_498dupTC mutation, which has been reported in members of a French family with HF . Normal adult human skin fibroblasts were purchased from PromoCell GmbH (Heidelberg, Germany). Fibroblasts were cultured in DMEM supplemented with 10% FBS, 2.0 mM L-glutamine, and 100U/ml penicillin/100 μg/ml streptomycin, and incubated at 37°C in humidified air with 5% CO2. Cells from trypsinized monolayers were seeded at 8-10 × 103 cells/cm2 and grown to confluence. For treatment with ferric ammonium citrate (FAC), confluent cells were incubated for 72 h with 100 μM FAC in DMEM in the absence of serum.
Confluent cell cultures were lysed in tris buffered saline (TBS) containing 1% sodium dodecyl sulfate (SDS) and protease inhibitors (PI, Complete, Roche, Indianapolis, IN). Protein extracts (30 μg) were run in 4-20% SDS-polyacrylamide gels (Pierce, Rockford, IL, USA) and transferred to nitrocellulose membranes (GE Healthcare, Piscataway, NJ, USA). Membranes were blocked for 1 h in TBS containing 0.1% Tween-20 and 5% non-fat dry milk, followed by an overnight incubation with primary antibody (ab). After washing in TBS containing 0.1% Tween-20, the membranes were incubated with peroxidase-conjugated secondary ab (1:5000; GE Healthcare) for 1 h. Membranes were developed using the ECL chemiluminescent detection system (GE Healthcare). Densitometric analyses were performed using the NIH ImageJ program and normalized against the signal obtained by re-probing the membranes with anti-β-actin abs (Sigma-Aldrich). Primary antibodies were: anti-Transferrin Receptor-1 (TfR1; 1:500; Zymed Laboratories, South San Francisco, CA), anti-divalent metal transporter-1 (DMT1, recognizing both +/- IRE isoforms; 1:250; Alpha Diagnostic International, San Antonio, TX), anti-ferroportin-1 (FPN; 1:250; Alpha Diagnostic International), anti-FTL (D-18, 1:250, Santa Cruz Biotechnology, Santa Cruz, CA), anti-mutant FTL (ab1283, 1:8000) that recognizes specifically the human mutant FTL chain , anti-FTH (1:2000; Abcam, Cambridge, MA), and anti β-actin (1:10000; Sigma, St. Louis, MO). Nomenclature of the proteins is according to http://BioIron.org.
Cultured fibroblasts were fixed in PBS + 4% paraformaldehyde (pH 7.4), at 4°C for 15 min and washed three times with PBS. Cells were permeabilized and blocked in 10% goat serum (Invitrogen), 2% bovine serum albumin (BSA) and 0.1% Triton X-100 in PBS and incubated with ab1283 (1:100) and mouse anti-α-tubulin (1:500; Sigma, St. Louis, MO). Secondary abs were: Alexa-Fluor488 goat anti-rabbit and Alexa-Fluor594 goat anti-mouse (Molecular Probes Inc, Eugene, OR). Fluorescence images were acquired with a Zeiss LSM 510 confocal microscope using an inverted 40× NA 1.2 objective.
Iron response element (IRE)-binding activity was analyzed by gel retardation assay as described [22,23]. Briefly, cultured confluent fibroblasts were trypsinized and homogenized in extraction buffer (10 mM Hepes, pH 7.5, 3 mM MgCl2, 40 mM NaCl, 5% glycerol, 1 mM dithiothreitol, and 0.2% Nonidet P-40) at 4°C. After lysis, samples were centrifuged for 2 min at 10,000 X g to remove nuclei. The cytoplasmic extracts were diluted to a protein concentration of 3 mg/mL in lysis buffer without Nonidet P-40. The RNA IRE probe was transcribed in vitro from a linearized plasmid template (kindly provided by Dr. K. Pantopoulos) using T7 RNA polymerase in the presence of [α-32P]UTP as described . For the RNA-protein complexes, 25 μg of cytoplasmic extract was incubated at room temperature with the radiolabeled ferritin IRE probe (25,000 cpm) in the absence or presence of 2% 2-mercaptoethanol (2-ME). After 10 min, heparin (50 μg) was added to the reaction to inhibit non-specific protein interactions with the probe and the incubation was continued for another 10 min. Unprotected probe was degraded by incubation with 1 U of RNase T1 for 10 min. RNA-protein complexes were analyzed in 6% non-denaturing polyacrylamide gels and visualized by autoradiography. Bands were scanned and the ratios of the intensity of the IRE-IRP complexes formed in the absence or presence of 2-ME were determined.
Total iron content was determined as previously described  with minor modifications. Briefly, cultured fibroblasts plated on 60 mm dishes were lysed in 0.9 ml of 50 mM NaOH for 2 h on a shaker in a humidified atmosphere. A standard curve was set using FAC standards (0-40 μM) in 10 mM HCl. Aliquots of cell lysates or standards were placed in 1.5 mL tubes and mixed with HCl or NaOH, respectively, to reach the same final concentration. Iron-releasing reagent (1.4M HCl:4.5% (w/v) KMnO4 in H2O) was added and the mixture incubated for 2 h at 60°C, in order to release iron-containing proteins. After cooling to room temperature, 60 μL of the iron-detection reagent (6.5 mM ferrozine, 6.5 mM neocuproine, 2.5 M ammonium acetate, and 1 M ascorbic acid dissolved in H2O) was added to each tube. After 30 min, 280 μL of the solution in each tube was transferred into a well of a 96-well plate and the absorbance was measured at 570 nm on a BioTek EL800 microplate reader (BioTek Instruments, Inc., Winooski, VT). The intracellular iron concentration was normalized against the protein content of the sample.
LIP was measured using the metal-sensitive fluorescence probe calcein [19,20] in attached cells as described  with minor modifications. Briefly, confluent cell monolayers were first treated for 72 h in the presence of vehicle or 100 μM FAC. The cells were washed twice with PBS and loaded with calcein-acetoxymethyl ester (Invitrogen) at a final concentration of 0.25 μM for 15 min at 37°C (from a 1 mM stock solution in dimethyl sulfoxide) in loading medium (DMEM without sodium bicarbonate, 20 mM Hepes pH 7.4, 1 mg/ml BSA). Cells were washed and loaded in measuring media (20 mM Hepes pH 7.4, 150 mM NaCl, 5 mM glucose). After reaching baseline (3 min) first fluorescence readings (F1) were taken using a Beckman DTX880 fluorimeter (Beckman Coulter Inc., Fullerton, CA) in bottom read technique with a fluorescein optical filter (excitation: 485 nm; emission: 535 nm). Finally, the cells were depleted of iron in the presence of the membrane-permeable iron chelator salicylaldehyde isonicotinoyl hydrazone (SIH), kindly provided by Dr. Prem Ponka  and a second measurement of fluorescence was performed (F2) after 20 min. The F2/F1 ratio was used as a relative indicator of LIP independent of the cell number and distribution within the wells.
ROS formation was quantified by measuring fluorescence intensity of cultures after loading cells with 5-(and-6)-chloromethyl-2',7'-dichlorodihydrofluorescein diacetate (CM-H2DCFDA; Molecular Probes) . CM-H2DCFDA, a cell-permeable indicator for reactive oxygen species, is hydrolyzed inside cells to a non-fluorescent compound which emits fluorescence when oxidized. Cultures were washed with Hank's Balanced Salt Solution (HBSS) containing calcium and magnesium. 10 μM DCFH-DA was loaded and incubated for 15 min at 37°C. Cultures were then washed in HBSS and fluorescence measurements were taken at 37°C using a Beckman DTX880 fluorimeter in bottom read technique with a fluorescein optical filter (excitation: 485 nm; emission: 535 nm). Background fluorescence from cultures subjected to sham dye incubation was subtracted from each recording.
All data are presented as the mean ± SD. Samples were run on duplicate or triplicate and each experiment was repeated at least three times. Statistical analysis was performed using the Student's t-test or a one-way analysis of variance followed by the Student's-Newman-Keuls test for multiple comparisons using GraphPad Prism version 4.03 (GraphPad Software Inc, La Jolla, CA). Differences were declared statistically significant if p < 0.05. When normality test failed, comparison of the means was performed by Weltch test.
The authors state that there is no actual or potential conflicts of interest including any financial, personal or other relationships with other people or organizations within five years of beginning the work submitted that could inappropriately influence (bias) their work. The authors do not have any non-financial competing interests (political, personal, religious, ideological, academic, intellectual, commercial or any other) to declare in relation to this manuscript.
AGB carried out experiments and analyzed data. TL and MBD extracted patients' fibroblasts and propagated them. BG critically read through the paper. AGB and RV designed the experiments and wrote the paper with assistance from all other authors. All authors read and approved the final manuscript.
We are very grateful to all patients who through their commitment made this study possible. The authors are grateful to Virginie Garcia and Marie-Ange Gauthie-Berges for their technical assistance and Holly J. Garringer and Martin A. Baraibar for helpful comments on the manuscript. We thank Dr. K. Pantopoulos for the pGEMI12.CAT plasmid and Dr. Prem Ponka for the iron chelator salicylaldehyde isonicotinoyl hydrazone. This study was supported by grants from the National Institute on Neurological Disorders and Stroke NS050227, NS063056 (RV) and the National Institute on Aging AG10133 (BG). The funding agencies had no influence over experimental design, data analysis or conclusions.