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      A role for keratins in supporting mitochondrial organization and function in skin keratinocytes

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          Abstract

          Mitochondria fulfill essential roles in ATP production, metabolic regulation, calcium signaling, generation of reactive oxygen species (ROS), and additional determinants of cellular health. Recent studies have highlighted a role for mitochondria during cell differentiation, including in skin epidermis. The observation of oxidative stress in keratinocytes from Krt16 null mouse skin, a model for pachyonychia congenita (PC)–associated palmoplantar keratoderma, prompted us to examine the role of Keratin (K) 16 protein and its partner K6 in regulating the structure and function of mitochondria. Electron microscopy revealed major anomalies in mitochondrial ultrastructure in late stage, E18.5, Krt6a/Krt6b null embryonic mouse skin. Follow-up studies utilizing biochemical, metabolic, and live imaging readouts showed that, relative to controls, skin keratinocytes null for Krt6a/Krt6b or Krt16 exhibit elevated ROS, reduced mitochondrial respiration, intracellular distribution differences, and altered movement of mitochondria within the cell. These findings highlight a novel role for K6 and K16 in regulating mitochondrial morphology, dynamics, and function and shed new light on the causes of oxidative stress observed in PC and related keratin-based skin disorders.

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          Most cited references51

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          T cell metabolism drives immunity

          Buck et al. discuss the role of lymphocyte metabolism on immune cell development and function.
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            Mitochondrial Cristae: Where Beauty Meets Functionality.

            Mitochondrial cristae are dynamic bioenergetic compartments whose shape changes under different physiological conditions. Recent discoveries have unveiled the relation between cristae shape and oxidative phosphorylation (OXPHOS) function, suggesting that membrane morphology modulates the organization and function of the OXPHOS system, with a direct impact on cellular metabolism. As a corollary, cristae-shaping proteins have emerged as potential modulators of mitochondrial bioenergetics, a concept confirmed by genetic experiments in mouse models of respiratory chain deficiency. Here, we review our knowledge of mitochondrial ultrastructural organization and how it impacts mitochondrial metabolism.
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              New consensus nomenclature for mammalian keratins

              Keratins are intermediate filament–forming proteins that provide mechanical support and fulfill a variety of additional functions in epithelial cells. In 1982, a nomenclature was devised to name the keratin proteins that were known at that point. The systematic sequencing of the human genome in recent years uncovered the existence of several novel keratin genes and their encoded proteins. Their naming could not be adequately handled in the context of the original system. We propose a new consensus nomenclature for keratin genes and proteins that relies upon and extends the 1982 system and adheres to the guidelines issued by the Human and Mouse Genome Nomenclature Committees. This revised nomenclature accommodates functional genes and pseudogenes, and although designed specifically for the full complement of human keratins, it offers the flexibility needed to incorporate additional keratins from other mammalian species.
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                Author and article information

                Contributors
                Role: Monitoring Editor
                Journal
                Mol Biol Cell
                Mol. Biol. Cell
                molbiolcell
                mbc
                mboc
                Molecular Biology of the Cell
                The American Society for Cell Biology
                1059-1524
                1939-4586
                15 May 2020
                : 31
                : 11
                : 1103-1111
                Affiliations
                [a ]Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109
                [c ]Department of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48109
                [f ]Department of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109
                [b ]Laboratory for Cellular and Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892
                [d ]Department of Pathology, University of Michigan, Ann Arbor, MI 48109
                [e ]Rogel Cancer Center, University of Michigan, Ann Arbor, MI 48109
                Åbo Akademi University
                Author notes

                Present addresses: Office of Research, University of Michigan Medical School, Ann Arbor, MI 48109;

                Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109;

                §Department of Molecular, Cellular and Developmental Biology, School of Medicine, Yale University, New Haven, CT 06511.

                *Address correspondence to: Pierre A. Coulombe ( coulombe@ 123456umich.edu ).
                Article
                E19-10-0565
                10.1091/mbc.E19-10-0565
                7353162
                32213122
                7f189b74-7430-49e2-8628-a886d8fb5954
                © 2020 Steen et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.

                This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.

                History
                : 18 October 2019
                : 10 March 2020
                : 13 March 2020
                Categories
                Brief Reports

                Molecular biology
                Molecular biology

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