Mitochondrial Contributions to Hematopoietic Stem Cell Aging

被引:35
作者
Morganti, Claudia [1 ,2 ,3 ,4 ]
Ito, Keisuke [1 ,2 ,3 ,4 ]
机构
[1] Albert Einstein Coll Med, Ruth L & David S Gottesman Inst Stem Cell & Regen, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Stem Cell Inst, Bronx, NY 10461 USA
[4] Albert Einstein Coll Med, Montefiore Med Ctr, Dept Med, Bronx, NY 10461 USA
基金
美国国家卫生研究院;
关键词
hematopoiesis; hematopoietic stem cell; aging; mitochondrial metabolism; stem cell exhaustion; ROS; inflammation; LIFE-SPAN; OXIDATIVE STRESS; DNA MUTATIONS; SELF-RENEWAL; CHRONIC INFLAMMATION; AUTOPHAGY MAINTAINS; AGE; DYSFUNCTION; PHENOTYPES; METABOLISM;
D O I
10.3390/ijms222011117
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial dysfunction and stem cell exhaustion are two hallmarks of aging. In the hematopoietic system, aging is linked to imbalanced immune response and reduced regenerative capacity in hematopoietic stem cells (HSCs), as well as an increased predisposition to a spectrum of diseases, including myelodysplastic syndrome and acute myeloid leukemia. Myeloid-biased differentiation and loss of polarity are distinct features of aged HSCs, which generally exhibit enhanced mitochondrial oxidative phosphorylation and increased production of reactive oxygen species (ROS), suggesting a direct role for mitochondria in the degenerative process. Here, we provide an overview of current knowledge of the mitochondrial mechanisms that contribute to age-related phenotypes in HSCs. These include mitochondrial ROS production, alteration/activation of mitochondrial metabolism, the quality control pathway of mitochondria, and inflammation. Greater understanding of the key machineries of HSC aging will allow us to identify new therapeutic targets for preventing, delaying, or even reversing aspects of this process.</p>
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页数:16
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共 169 条
[1]   Prediction of acute myeloid leukaemia risk in healthy individuals [J].
Abelson, Sagi ;
Collord, Grace ;
Ng, Stanley W. K. ;
Weissbrod, Omer ;
Cohen, Netta Mendelson ;
Niemeyer, Elisabeth ;
Barda, Noam ;
Zuzarte, Philip C. ;
Heisler, Lawrence ;
Sundaravadanam, Yogi ;
Luben, Robert ;
Hayat, Shabina ;
Wang, Ting Ting ;
Zhao, Zhen ;
Cirlan, Julia ;
Pugh, Trevor J. ;
Soave, David ;
Ng, Karen ;
Latimer, Calli ;
Hardy, Claire ;
Raine, Keiran ;
Jones, David ;
Hoult, Diana ;
Britten, Abigail ;
McPherson, John D. ;
Johansson, Mattias ;
Mbabaali, Faridah ;
Eagles, Jenna ;
Millers, Jessica K. ;
Pasternack, Danielle ;
Timms, Lee ;
Krzyzanowski, Paul ;
Awadalla, Philip ;
Costa, Rui ;
Segal, Eran ;
Bratman, Scott, V ;
Beer, Philip ;
Behjati, Sam ;
Martincorena, Inigo ;
Wang, Jean C. Y. ;
Bowles, Kristian M. ;
Ramon Quiros, J. ;
Karakatsani, Anna ;
La Vecchia, Carlo ;
Trichopoulou, Antonia ;
Salamanca-Fernandez, Elena ;
Huerta, Jose M. ;
Barricarte, Aurelio ;
Travis, Ruth C. ;
Tumino, Rosario .
NATURE, 2018, 559 (7714) :400-+
[2]   MtDNA mutagenesis impairs elimination of mitochondria during erythroid maturation leading to enhanced erythrocyte destruction [J].
Ahlqvist, K. J. ;
Leoncini, S. ;
Pecorelli, A. ;
Wortmann, S. B. ;
Ahola, S. ;
Forsstrom, S. ;
Guerranti, R. ;
De Felice, C. ;
Smeitink, J. ;
Ciccoli, L. ;
Hamalainen, R. H. ;
Suomalainen, A. .
NATURE COMMUNICATIONS, 2015, 6
[3]   Somatic Progenitor Cell Vulnerability to Mitochondrial DNA Mutagenesis Underlies Progeroid Phenotypes in Polg Mutator Mice [J].
Ahlqvist, Kati J. ;
Hamalainen, Riikka H. ;
Yatsuga, Shuichi ;
Uutela, Marko ;
Terzioglu, Mugen ;
Gotz, Alexandra ;
Forsstrom, Saara ;
Salven, Petri ;
Angers-Loustau, Alexandre ;
Kopra, Outi H. ;
Tyynismaa, Henna ;
Larsson, Nils-Goran ;
Wartiovaara, Kirmo ;
Prolla, Tomas ;
Trifunovic, Aleksandra ;
Suomalainen, Anu .
CELL METABOLISM, 2012, 15 (01) :100-109
[4]   Role of mitochondria ROS generation in ethanol-induced NLRP3 inflammasome activation and cell death in astroglial cells [J].
Alfonso-Loeches, Silvia ;
Urena-Peralta, Juan R. ;
Jose Morillo-Bargues, Maria ;
Oliver-De La Cruz, Jorge ;
Guerri, Consuelo .
FRONTIERS IN CELLULAR NEUROSCIENCE, 2014, 8
[5]   SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J].
ANDERSON, S ;
BANKIER, AT ;
BARRELL, BG ;
DEBRUIJN, MHL ;
COULSON, AR ;
DROUIN, J ;
EPERON, IC ;
NIERLICH, DP ;
ROE, BA ;
SANGER, F ;
SCHREIER, PH ;
SMITH, AJH ;
STADEN, R ;
YOUNG, IG .
NATURE, 1981, 290 (5806) :457-465
[6]   The mitochondrial respiratory chain is essential for haematopoietic stem cell function [J].
Anso, Elena ;
Weinberg, Samuel E. ;
Diebold, Lauren P. ;
Thompson, Benjamin J. ;
Malinge, Sebastien ;
Schumacker, Paul T. ;
Liu, Xin ;
Zhang, Yuannyu ;
Shao, Zhen ;
Steadman, Mya ;
Marsh, Kelly M. ;
Xu, Jian ;
Crispino, John D. ;
Chandel, Navdeep S. .
NATURE CELL BIOLOGY, 2017, 19 (06) :614-+
[7]   Sensitivity of hematopoietic stem cells to mitochondrial dysfunction by SdhD gene deletion [J].
Antonio Bejarano-Garcia, Jose ;
Millan-Ucles, Africa ;
Rosado, Ivan V. ;
Ignacio Sanchez-Abarca, Luis ;
Caballero-Velazquez, Teresa ;
Jose Duran-Galvan, Maria ;
Antonio Perez-Simon, Jose ;
Piruat, Jose I. .
CELL DEATH & DISEASE, 2016, 7 :e2516-e2516
[8]   Upregulation of the Autophagy Adaptor p62/SQSTM1 Prolongs Health and Lifespan in Middle-Aged Drosophila [J].
Aparicio, Ricardo ;
Rana, Anil ;
Walker, David W. .
CELL REPORTS, 2019, 28 (04) :1029-+
[9]   Neuropathy of haematopoietic stem cell niche is essential for myeloproliferative neoplasms [J].
Arranz, Lorena ;
Sanchez-Aguilera, Abel ;
Martin-Perez, Daniel ;
Isern, Joan ;
Langa, Xavier ;
Tzankov, Alexandar ;
Lundberg, Pontus ;
Muntion, Sandra ;
Tzeng, Yi-Shiuan ;
Lai, Dar-Ming ;
Schwaller, Juerg ;
Skoda, Radek C. ;
Mendez-Ferrer, Simon .
NATURE, 2014, 512 (7512) :78-+
[10]   Mitochondria, oxidants, and aging [J].
Balaban, RS ;
Nemoto, S ;
Finkel, T .
CELL, 2005, 120 (04) :483-495