Mitochondria as signaling organelles

被引:386
作者
Chandel, Navdeep S. [1 ]
机构
[1] Northwestern Univ, Dept Med, Sect Pulm & Crit Care Med, Feinberg Sch Med, Chicago, IL 60611 USA
来源
BMC BIOLOGY | 2014年 / 12卷
关键词
HYPOXIA-INDUCED TRANSCRIPTION; INCREASING OXIDATIVE STRESS; NF-KAPPA-B; LIFE-SPAN; CYTOCHROME-C; STEM-CELLS; ENDOPLASMIC-RETICULUM; CELLULAR-METABOLISM; OXIDANTS; PROTEIN;
D O I
10.1186/1741-7007-12-34
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Almost 20 years ago, the discovery that mitochondrial release of cytochrome c initiates a cascade that leads to cell death brought about a wholesale change in how cell biologists think of mitochondria. Formerly viewed as sites of biosynthesis and bioenergy production, these double membrane organelles could now be thought of as regulators of signal transduction. Within a few years, multiple other mitochondria- centric signaling mechanisms have been proposed, including release of reactive oxygen species and the scaffolding of signaling complexes on the outer mitochondrial membrane. It has also been shown that mitochondrial dysfunction causes induction of stress responses, bolstering the idea that mitochondria communicate their fitness to the rest of the cell. In the past decade, multiple new modes of mitochondrial signaling have been discovered. These include the release of metabolites, mitochondrial motility and dynamics, and interaction with other organelles such as endoplasmic reticulum in regulating signaling. Collectively these studies have established that mitochondria- dependent signaling has diverse physiological and pathophysiological outcomes. This review is a brief account of recent work in mitochondria- dependent signaling in the historical framework of the early studies.
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页数:7
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共 82 条
[61]   Inflammasornes and Metabolic Disorders: Old Genes in Modern Diseases [J].
Robbins, Gregory R. ;
Wen, Haitao ;
Ting, Jenny P. -Y. .
MOLECULAR CELL, 2014, 54 (02) :297-308
[62]   Linking functional decline of telomeres, mitochondria and stem cells during ageing [J].
Sahin, Erguen ;
DePinho, Ronald A. .
NATURE, 2010, 464 (7288) :520-528
[63]   Epigenetic Silencing Mediates Mitochondria Stress-Induced Longevity [J].
Schroeder, Elizabeth A. ;
Raimundo, Nuno ;
Shadel, Gerald S. .
CELL METABOLISM, 2013, 17 (06) :954-964
[64]   Glucose restriction extends Caenorhabditis elegans life span by inducing mitochondrial respiration and increasing oxidative stress [J].
Schulz, Tim J. ;
Zarse, Kim ;
Voigt, Anja ;
Urban, Nadine ;
Birringer, Marc ;
Ristow, Michael .
CELL METABOLISM, 2007, 6 (04) :280-293
[65]   Physiological Roles of Mitochondrial Reactive Oxygen Species [J].
Sena, Laura A. ;
Chandel, Navdeep S. .
MOLECULAR CELL, 2012, 48 (02) :158-167
[66]   Identification and characterization of MAVS, a mitochondrial antiviral signaling protein that activates NF-κB and IRF3 [J].
Seth, RB ;
Sun, LJ ;
Ea, CK ;
Chen, ZJJ .
CELL, 2005, 122 (05) :669-682
[67]   OXIDATIVE DAMAGE AND MITOCHONDRIAL DECAY IN AGING [J].
SHIGENAGA, MK ;
HAGEN, TM ;
AMES, BN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (23) :10771-10778
[68]   Mechanisms that Regulate Stem Cell Aging and Life Span [J].
Signer, Robert A. J. ;
Morrison, Sean J. .
CELL STEM CELL, 2013, 12 (02) :152-165
[69]   REQUIREMENT FOR GENERATION OF H2O2 FOR PLATELET-DERIVED GROWTH-FACTOR SIGNAL-TRANSDUCTION [J].
SUNDARESAN, M ;
YU, ZX ;
FERRANS, VJ ;
IRANI, K ;
FINKEL, T .
SCIENCE, 1995, 270 (5234) :296-299
[70]   Pattern Recognition Receptors and Inflammation [J].
Takeuchi, Osamu ;
Akira, Shizuo .
CELL, 2010, 140 (06) :805-820