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Lethal Cardiomyopathy in Mice Lacking Transferrin Receptor in the Heart
Open accessAbstract
Both iron overload and iron deficiency have been associated with cardiomyopathy and heart failure, but cardiac iron utilization is incompletely understood. We hypothesized that the transferrin receptor (Tfr1) might play a role in cardiac iron uptake and used gene targeting to examine the role of Tfr1 in vivo. Surprisingly, we found that decreased iron, due to inactivation of Tfr1, was associated with severe cardiac consequences. Mice lacking Tfr1 in the heart died in the second week of life and had cardiomegaly, poor cardiac function, failure of mitochondrial respiration, and ineffective mitophagy. The phenotype could only be rescued by aggressive iron therapy, but it was ameliorated by administration of nicotinamide riboside, an NAD precursor. Our findings underscore the importance of both Tfr1 and iron in the heart, and may inform therapy for patients with heart failure.
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Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., Paulovich, A., Pomeroy, S. L., Golub, T. R., Lander, E. S., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506580102 · Cited by 53,625
Mootha, V. K., Lindgren, C. M., Eriksson, K.-F., Subramanian, A., Sihag, S., Lehar, J., Puigserver, P., Carlsson, E., Ridderstråle, M., Laurila, E., et al. (2003) · Nature Genetics · doi:10.1038/ng1180 · Cited by 10,197
Wu, Z., Puigserver, P., Andersson, U., Zhang, C., Adelmant, G., Mootha, V., Troy, A., Cinti, S., Lowell, B., Scarpulla, R. C., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)80611-x · Cited by 4,139
Mitochondria: In Sickness and in Health
Nunnari, J., & Suomalainen, A. (2012) · Cell · doi:10.1016/j.cell.2012.02.035 · Cited by 3,479
Oxygen sensing by metazoans: the central role of the HIF hydroxylase pathway.
Kaelin, W. G., & Ratcliffe, P. J. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.04.009 · Cited by 3,251
Untersuchungen uber die Harnstoffbildung im Tierkörper
Krebs, H. A., & Henseleit, K. (1932) · Hoppe-Seyler´s Zeitschrift für physiologische Chemie · doi:10.1515/bchm2.1932.210.1-2.33 · Cited by 3,100
Hentze, M. W., Muckenthaler, M. U., & Andrews, N. C. (2004) · Cell · doi:10.1016/s0092-8674(04)00343-5 · Cited by 1,736
Self-citationMitochondrial outer-membrane protein FUNDC1 mediates hypoxia-induced mitophagy in mammalian cells
Liu, L., Feng, D., Chen, G., Chen, M., Zheng, Q., Song, P., Ma, Q., Zhu, C., Wang, R., Qi, W., et al. (2012) · Nature Cell Biology · doi:10.1038/ncb2422 · Cited by 1,684
Gomes, A. P., Price, N. L., Ling, A. J. Y., Moslehi, J. J., Montgomery, M. K., Rajman, L., White, J. P., Teodoro, J. S., Wrann, C. D., Hubbard, B. P., et al. (2013) · Cell · doi:10.1016/j.cell.2013.11.037 · Cited by 1,482
Nix is a selective autophagy receptor for mitochondrial clearance
Novak, I., Kirkin, V., McEwan, D. G., Zhang, J., Wild, P., Rozenknop, A., Rogov, V., Löhr, F., Popovic, D., Occhipinti, A., et al. (2010) · The EMBO Reports · doi:10.1038/embor.2009.256 · Cited by 1,309 · cited 4×
“Autophagy-related proteins LC3-II, p62, Fundc1, Nix, Ulk-1 and Cisd2, showed no significant differences (Fig 6C–”
BackgroundInfluentialPeroxisome proliferator–activated receptor γ coactivator-1 promotes cardiac mitochondrial biogenesis
Lehman, J. J., Barger, P. M., Kovacs, A., Saffitz, J. E., Medeiros, D. M., & Kelly, D. P. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10268 · Cited by 1,285
Cantó, C., Houtkooper, R. H., Pirinen, E., Youn, D. Y., Oosterveer, M. H., Cen, Y., Fernandez-Marcos, P. J., Yamamoto, H., Andreux, P. A., Cettour-Rose, P., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.04.022 · Cited by 1,238
Self-citationYamane, K., Toumazou, C., Tsukada, Y.-I., Erdjument-Bromage, H., Tempst, P., Wong, J., & Zhang, Y. (2006) · Cell · doi:10.1016/j.cell.2006.03.027 · Cited by 837
Weidberg, H., Shvets, E., Shpilka, T., Shimron, F., Shinder, V., & Elazar, Z. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.74 · Cited by 777
Expression of the gene encoding the proapoptotic Nip3 protein is induced by hypoxia
Bruick, R. K. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.16.9082 · Cited by 773
Puccio, H., Simon, D., Cossée, M., Criqui-Filipe, P., Tiziano, F., Melki, J., Hindelang, C., Matyas, R., Rustin, P., & Koenig, M. (2001) · Nature Genetics · doi:10.1038/84818 · Cited by 738
Defective Mitophagy in XPA via PARP-1 Hyperactivation and NAD+/SIRT1 Reduction
Fang, E. F., Scheibye-Knudsen, M., Brace, L. E., Kassahun, H., SenGupta, T., Nilsen, H., Mitchell, J. R., Croteau, D. L., & Bohr, V. A. (2014) · Cell · doi:10.1016/j.cell.2014.03.026 · Cited by 711
Arany, Z., He, H., Lin, J., Hoyer, K., Handschin, C., Toka, O., Ahmad, F., Matsui, T., Chin, S., Wu, P.-H., et al. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.03.002 · Cited by 694
Agah, R., Frenkel, P. A., French, B. A., Michael, L. H., Overbeek, P. A., & Schneider, M. D. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119509 · Cited by 606
Transferrin receptor is necessary for development of erythrocytes and the nervous system
Levy, J. E., Jin, O., Fujiwara, Y., Kuo, F., & Andrews, N. (1999) · Nature Genetics · doi:10.1038/7727 · Cited by 574
Self-citationULK1 translocates to mitochondria and phosphorylates FUNDC1 to regulate mitophagy
Wu, W., Tian, W., Hu, Z., Chen, G., Huang, L., Li, W., Zhang, X., Xue, P., Zhou, C., Liu, L., et al. (2014) · The EMBO Reports · doi:10.1002/embr.201438501 · Cited by 574
Lipin 1 is an inducible amplifier of the hepatic PGC-1α/PPARα regulatory pathway
Finck, B. N., Gropler, M. C., Chen, Z., Leone, T. C., Croce, M. A., Harris, T. E., Lawrence, J. C., & Kelly, D. P. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.08.005 · Cited by 554
Selective expression of the large neutral amino acid transporter at the blood–brain barrier
Boado, R. J., Li, J. Y., Nagaya, M., Zhang, C., & Pardridge, W. M. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.21.12079 · Cited by 481
Mitochondrial Complex I Deficiency Increases Protein Acetylation and Accelerates Heart Failure
Karamanlidis, G., Lee, C. F., Garcia-Menendez, L., Kolwicz, S. C., Suthammarak, W., Gong, G., Sedensky, M. M., Morgan, P. G., Wang, W., & Tian, R. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.07.002 · Cited by 468
Deactivation of peroxisome proliferator–activated receptor-α during cardiac hypertrophic growth
Barger, P. M., Brandt, J. M., Leone, T. C., Weinheimer, C. J., & Kelly, D. P. (2000) · Journal of Clinical Investigation · doi:10.1172/jci9056 · Cited by 464
Coordination of PGC-1β and iron uptake in mitochondrial biogenesis and osteoclast activation
Ishii, K.-A., Fumoto, T., Iwai, K., Takeshita, S., Ito, M., Shimohata, N., Aburatani, H., Taketani, S., Lelliott, C. J., Vidal-Puig, A., et al. (2009) · Nature Medicine · doi:10.1038/nm.1910 · Cited by 410
Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3
Khan, N. A., Auranen, M., Paetau, I., Pirinen, E., Euro, L., Forsström, S., Pasila, L., Velagapudi, V., Carroll, C. J., Auwerx, J., et al. (2014) · EMBO Molecular Medicine · doi:10.1002/emmm.201403943 · Cited by 385
Biochemical Assays of Respiratory Chain Complex Activity
Kirby, D. M., Thorburn, D. R., Turnbull, D. M., & Taylor, R. W. (2007) · Methods in Cell Biology · doi:10.1016/s0091-679x(06)80004-x · Cited by 384
Janssen, A. J., Trijbels, F. J., Sengers, R. C., Smeitink, J. A., van den Heuvel, L. P., Wintjes, L. T., Stoltenborg-Hogenkamp, B. J., & Rodenburg, R. J. (2007) · Clinical Chemistry · doi:10.1373/clinchem.2006.078873 · Cited by 373
A mouse model of juvenile hemochromatosis
Huang, F. W. (2005) · Journal of Clinical Investigation · doi:10.1172/jci25049 · Cited by 365
NAD+-Dependent Activation of Sirt1 Corrects the Phenotype in a Mouse Model of Mitochondrial Disease
Cerutti, R., Pirinen, E., Lamperti, C., Marchet, S., Sauve, A. A., Li, W., Leoni, V., Schon, E. A., Dantzer, F., Auwerx, J., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.04.001 · Cited by 343 · cited 1×
“The response to NR is reminiscent of other studies where it increases NAD, sirtuin activity and mitochondrial biogenesis (Canto et al., 2012; Cerutti et al., 2014).”
BackgroundSelf-citationHexokinase-II Positively Regulates Glucose Starvation-Induced Autophagy through TORC1 Inhibition
Roberts, D. J., Tan-Sah, V. P., Ding, E. Y., Smith, J. M., & Miyamoto, S. (2014) · Molecular Cell · doi:10.1016/j.molcel.2013.12.019 · Cited by 330
Coordinated Regulation of Iron-Controlling Genes, H-Ferritin and IRP2 , by c-MYC
Wu, K.-J., Polack, A., & Dalla-Favera, R. (1999) · Science · doi:10.1126/science.283.5402.676 · Cited by 326
Le, N. T. V., & Richardson, D. R. (2004) · Blood · doi:10.1182/blood-2004-05-1866 · Cited by 321
Regula, K. M., Ens, K., & Kirshenbaum, L. A. (2002) · Circulation Research · doi:10.1161/01.res.0000029232.42227.16 · Cited by 318
Tumbarello, D. A., Waxse, B. J., Arden, S. D., Bright, N. A., Kendrick-Jones, J., & Buss, F. (2012) · Nature Cell Biology · doi:10.1038/ncb2589 · Cited by 301
Antagonism of Beclin 1‐dependent autophagy by BCL‐2 at the endoplasmic reticulum requires NAF‐1
Chang, N. C., Nguyen, M., Germain, M., & Shore, G. C. (2010) · The EMBO Journal · doi:10.1038/emboj.2009.369 · Cited by 281
Activation of Transferrin Receptor 1 by c-Myc Enhances Cellular Proliferation and Tumorigenesis
O'Donnell, K. A., Yu, D., Zeller, K. I., Kim, J.-W., Racke, F., Thomas-Tikhonenko, A., & Dang, C. V. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.6.2373-2386.2006 · Cited by 253
Tanida, I., Ueno, T., & Kominami, E. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m407016200 · Cited by 243
Torrance, J. D. (1980) · Medical Entomology and Zoology · Cited by 234
Erbel, P. J. A., Card, P. B., Karakuzu, O., Bruick, R. K., & Gardner, K. H. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2533374100 · Cited by 228
The molecular defect in hypotransferrinemic mice
Trenor, C. C., Campagna, D. R., Sellers, V. M., Andrews, N. C., & Fleming, M. D. (2000) · Blood · doi:10.1182/blood.v96.3.1113 · Cited by 189
Self-citationIron and Copper in Mitochondrial Diseases
Xu, W., Barrientos, T., & Andrews, N. C. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.02.004 · Cited by 183
Self-citationStehling, O., Mascarenhas, J., Vashisht, A. A., Sheftel, A. D., Niggemeyer, B., Rösser, R., Pierik, A. J., Wohlschlegel, J. A., & Lill, R. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.06.015 · Cited by 170
Lipin-1 regulates autophagy clearance and intersects with statin drug effects in skeletal muscle
Zhang, P., Verity, M. A., & Reue, K. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.05.003 · Cited by 166
Cardiac Involvement in Hemochromatosis
Gulati, V., Harikrishnan, P., Palaniswamy, C., Aronow, W. S., Jain, D., & Frishman, W. H. (2013) · Cardiology in Review · doi:10.1097/crd.0b013e3182a67805 · Cited by 150
Quantitative analysis of autophagy-related protein stoichiometry by fluorescence microscopy
Geng, J., Baba, M., Nair, U., & Klionsky, D. J. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200711112 · Cited by 129
Kachhap, S. K., Faith, D., Qian, D. Z., Shabbeer, S., Galloway, N. L., Пили, Р., Denmeade, S. R., Marzo, A. M. D., & Carducci, M. A. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000844 · Cited by 127
Chi, Y., & Sauve, A. A. (2013) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e32836510c0 · Cited by 126
Self-citationTransferrin receptor 1 is differentially required in lymphocyte development
Ned, R. M., Swat, W., & Andrews, N. C. (2003) · Blood · doi:10.1182/blood-2003-04-1086 · Cited by 120
Self-citationCellular and functional defects in a mouse model of heart failure
Esposito, G., Santana, L. F., Dilly, K. W., Cruz, J. S., Mao, L., Lederer, W. J., & Rockman, H. A. (2000) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2000.279.6.h3101 · Cited by 120
Self-citationYang, T., Chan, N. Y., & Sauve, A. A. (2007) · Journal of Medicinal Chemistry · doi:10.1021/jm701001c · Cited by 116
Self-citationSahni, S., Bae, D.-H., Lane, D. J. R., Kovačević, Ž., Kalinowski, D. S., Jansson, P. J., & Richardson, D. R. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.529511 · Cited by 101
Noncanonical role of transferrin receptor 1 is essential for intestinal homeostasis
Chen, A. C., Donovan, A., Ned, R. M., & Andrews, N. C. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1511701112 · Cited by 98
Self-citationNemoto, T., Tanida, I., Tanida-Miyake, E., Minematsu‐Ikeguchi, N., Yokota, M., Ohsumi, M., Ueno, T., & Kominami, E. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300550200 · Cited by 90
Histone Demethylase JHDM2A Is Involved in Male Infertility and Obesity
Okada, Y., Tateishi, K., & Zhang, Y. (2010) · Journal of Andrology · doi:10.2164/jandrol.109.008052 · Cited by 86
Rensvold, J. W., Ong, S.-E., Jeevananthan, A., Carr, S. A., Mootha, V. K., & Pagliarini, D. J. (2013) · Cell Reports · doi:10.1016/j.celrep.2012.11.029 · Cited by 82
Autophagy and mitophagy in the myocardium: therapeutic potential and concerns
Jimenez, R. E., Kubli, D. A., & Gustafsson, Å. B. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12477 · Cited by 77
Transcriptional regulation of metabolic processes: implications for cardiac metabolism
van Bilsen, M., Vusse, G. J., & Reneman, R. S. (1998) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240050739 · Cited by 76
ATG16L1 meets ATG9 in recycling endosomes
Puri, C., Renna, M., Bento, C. F., Moreau, K., & Rubinsztein, D. C. (2013) · Autophagy · doi:10.4161/auto.27174 · Cited by 75
Ermak, G., Sojitra, S., Yin, F., Cadenas, E., Cuervo, A. M., & Davies, K. J. A. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.305342 · Cited by 70
Mizutani, A., Furukawa, T., Adachi, Y., Ikehara, S., & Taketani, S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m111431200 · Cited by 69
Spinazzi, M., Casarin, A., Pertegato, V., Ermani, M., Salviati, L., & Angelini, C. I. (2011) · Mitochondrion · doi:10.1016/j.mito.2011.07.006 · Cited by 61
Dietary Iron Deficiency Results in Cardiac Eccentric Hypertrophy in Rats
Medeiros, D. M., & Beard, J. L. (1998) · Experimental Biology and Medicine · doi:10.3181/00379727-218-44306 · Cited by 41
Yan, L., Yang, H., Li, Y., Duan, H., Wu, J., Qian, P., Li, B., & Wang, S. (2014) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000000121 · Cited by 26
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Metadata
- Authors
- Xu, W., Barrientos, T., Mao, L., Rockman, H. A., Sauve, A. A., & Andrews, N. C.
- Venue
- Cell Reports
- Publisher
- Elsevier BV
- Published
- 2015-10
- Volume
- 13
- Issue
- 3
- Pages
- 533-545
- ISSN
- 2211-1247 (ISSN-L)
- OpenAlex
- W1910071664
- Cited by
- 275
- References
- 65
- FWCI
- 15.15
- Type
- journal article
- Language
- en
- Open access
- gold
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