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      Dysregulated Mitochondrial Dynamics and Metabolism in Obesity, Diabetes, and Cancer

      review-article
      1 , 1 , 2 , *
      Frontiers in Endocrinology
      Frontiers Media S.A.
      energy metabolism, TCA cycle, mitochondrial dynamics, GTPase, mdivi-1

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          Abstract

          Metabolism describes the life-sustaining chemical reactions in organisms that provide both energy and building blocks for cellular survival and proliferation. Dysregulated metabolism leads to many life-threatening diseases including obesity, diabetes, and cancer. Mitochondria, subcellular organelles, contain the central energy-producing metabolic pathway, the tricarboxylic acid (TCA) cycle. Also, mitochondria exist in a dynamic network orchestrated by extracellular nutrient levels and intracellular energy needs. Upon stimulation, mitochondria undergo consistent interchange through fusion (small to big) and fission (big to small) processes. Mitochondrial fusion is primarily controlled by three GTPases, mitofusin 1 (Mfn1), Mfn2, and optic atrophy 1 (Opa1), while mitochondrial fission is primarily regulated by GTPase dynamin-related protein 1 (Drp1). Dysregulated activity of these GTPases results in disrupted mitochondrial dynamics and cellular metabolism. This review will update the metabolic roles of these GTPases in obesity, diabetes, and cancer.

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          Most cited references67

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          On the origin of cancer cells.

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            Chemical inhibition of the mitochondrial division dynamin reveals its role in Bax/Bak-dependent mitochondrial outer membrane permeabilization.

            Mitochondrial fusion and division play important roles in the regulation of apoptosis. Mitochondrial fusion proteins attenuate apoptosis by inhibiting release of cytochrome c from mitochondria, in part by controlling cristae structures. Mitochondrial division promotes apoptosis by an unknown mechanism. We addressed how division proteins regulate apoptosis using inhibitors of mitochondrial division identified in a chemical screen. The most efficacious inhibitor, mdivi-1 (for mitochondrial division inhibitor) attenuates mitochondrial division in yeast and mammalian cells by selectively inhibiting the mitochondrial division dynamin. In cells, mdivi-1 retards apoptosis by inhibiting mitochondrial outer membrane permeabilization. In vitro, mdivi-1 potently blocks Bid-activated Bax/Bak-dependent cytochrome c release from mitochondria. These data indicate the mitochondrial division dynamin directly regulates mitochondrial outer membrane permeabilization independent of Drp1-mediated division. Our findings raise the interesting possibility that mdivi-1 represents a class of therapeutics for stroke, myocardial infarction, and neurodegenerative diseases.
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              Mitochondrial dynamics--mitochondrial fission and fusion in human diseases.

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                Author and article information

                Contributors
                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrinol.
                Frontiers in Endocrinology
                Frontiers Media S.A.
                1664-2392
                03 September 2019
                2019
                : 10
                : 570
                Affiliations
                [1] 1Department of Molecular and Cellular Endocrinology, Diabetes and Metabolism Research Institute , Duarte, CA, United States
                [2] 2Comprehensive Cancer Center, City of Hope Medical Center , Duarte, CA, United States
                Author notes

                Edited by: Mei Kong, University of California, Irvine, United States

                Reviewed by: Jiangbin Ye, Stanford University, United States; Vanina Romanello, Veneto Institute of Molecular Medicine (VIMM), Italy

                *Correspondence: Lei Jiang ljiang@ 123456coh.org

                This article was submitted to Cellular Endocrinology, a section of the journal Frontiers in Endocrinology

                Article
                10.3389/fendo.2019.00570
                6734166
                31551926
                f200783a-2ac3-436c-ab7b-fe41fa8621ed
                Copyright © 2019 Dai and Jiang.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 13 March 2019
                : 05 August 2019
                Page count
                Figures: 1, Tables: 2, Equations: 0, References: 127, Pages: 10, Words: 8151
                Categories
                Endocrinology
                Review

                Endocrinology & Diabetes
                energy metabolism,tca cycle,mitochondrial dynamics,gtpase,mdivi-1
                Endocrinology & Diabetes
                energy metabolism, tca cycle, mitochondrial dynamics, gtpase, mdivi-1

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