Literature DB >> 27068470

The Mitochondrial Respiratory Chain Is Required for Organismal Adaptation to Hypoxia.

Robert B Hamanaka1, Samuel E Weinberg1, Colleen R Reczek1, Navdeep S Chandel2.   

Abstract

Hypoxia-inducible factors (HIFs) are crucial for cellular and organismal adaptation to hypoxia. The mitochondrial respiratory chain is the largest consumer of oxygen in most mammalian cells; however, it is unknown whether the respiratory chain is necessary for in vivo activation of HIFs and organismal adaptation to hypoxia. HIF-1 activation in the epidermis has been shown to be a key regulator of the organismal response to hypoxic conditions, including renal production of erythropoietin (Epo). Therefore, we conditionally deleted expression of TFAM in mouse epidermal keratinocytes. TFAM is required for maintenance of the mitochondrial genome, and TFAM-null cells are respiratory deficient. TFAM loss in epidermal keratinocytes reduced epidermal levels of HIF-1α protein and diminished the hypoxic induction of HIF-dependent transcription in epidermis. Furthermore, epidermal TFAM deficiency impaired hypoxic induction of renal Epo expression. Our results demonstrate that the mitochondrial respiratory chain is essential for in vivo HIF activation and organismal adaptation to hypoxia.
Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27068470      PMCID: PMC4838509          DOI: 10.1016/j.celrep.2016.03.044

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  31 in total

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Authors:  Christopher T Minson
Journal:  Adv Exp Med Biol       Date:  2003       Impact factor: 2.622

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Authors:  Andrew S Cowburn; Norihiko Takeda; Adam T Boutin; Jung-Whan Kim; Jane C Sterling; Manando Nakasaki; Mark Southwood; Ananda W Goldrath; Colin Jamora; Victor Nizet; Edwin R Chilvers; Randall S Johnson
Journal:  Proc Natl Acad Sci U S A       Date:  2013-10-07       Impact factor: 11.205

3.  Superoxide generated at mitochondrial complex III triggers acute responses to hypoxia in the pulmonary circulation.

Authors:  Gregory B Waypa; Jeremy D Marks; Robert D Guzy; Paul T Mungai; Jacqueline M Schriewer; Danijela Dokic; Molly K Ball; Paul T Schumacker
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4.  Redistribution of intracellular oxygen in hypoxia by nitric oxide: effect on HIF1alpha.

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Journal:  Science       Date:  2003-12-12       Impact factor: 47.728

5.  Epidermal sensing of oxygen is essential for systemic hypoxic response.

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Journal:  Cell       Date:  2008-04-18       Impact factor: 41.582

6.  A chemical genomics screen highlights the essential role of mitochondria in HIF-1 regulation.

Authors:  Xiaoyu Lin; Caroline A David; Jennifer B Donnelly; Mike Michaelides; Navdeep S Chandel; Xiaoli Huang; Usha Warrior; Frank Weinberg; Kathryn V Tormos; Stephen W Fesik; Yu Shen
Journal:  Proc Natl Acad Sci U S A       Date:  2008-01-02       Impact factor: 11.205

7.  Desferrioxamine induces erythropoietin gene expression and hypoxia-inducible factor 1 DNA-binding activity: implications for models of hypoxia signal transduction.

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Journal:  J Invest Dermatol       Date:  2014-07-07       Impact factor: 8.551

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Review 5.  Mitochondria control acute and chronic responses to hypoxia.

Authors:  G S McElroy; N S Chandel
Journal:  Exp Cell Res       Date:  2017-03-19       Impact factor: 3.905

Review 6.  Mitochondrial Uncoupling Proteins: Subtle Regulators of Cellular Redox Signaling.

Authors:  Petr Ježek; Blanka Holendová; Keith D Garlid; Martin Jabůrek
Journal:  Antioxid Redox Signal       Date:  2018-03-14       Impact factor: 8.401

7.  Molecular mechanisms of retinal ischemia.

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8.  Succinate Dehydrogenase Supports Metabolic Repurposing of Mitochondria to Drive Inflammatory Macrophages.

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9.  Oxidative Stress and Hypoxia Modify Mitochondrial Homeostasis During Glaucoma.

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10.  LKB1/STK11 Is a Tumor Suppressor in the Progression of Myeloproliferative Neoplasms.

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Journal:  Cancer Discov       Date:  2021-02-12       Impact factor: 39.397

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