Hematopoietic stem cell aging

被引:48
作者
Geiger, Hartmut [1 ,2 ,3 ,4 ]
Denkinger, Michael [5 ]
Schirmbeck, Reinhold [6 ]
机构
[1] Univ Ulm, Inst Mol Med Stem Cell & Aging, D-89069 Ulm, Germany
[2] Univ Ulm, Aging Res Ctr, D-89069 Ulm, Germany
[3] Cincinnati Childrens Hosp Med Ctr, Div Expt Hematol & Canc Biol, Cincinnati, OH 45229 USA
[4] Univ Cincinnati, Cincinnati, OH USA
[5] Univ Ulm, Geriatr Ctr, AGAPLESION Bethesda Clin, D-89069 Ulm, Germany
[6] Univ Hosp Ulm, Dept Internal Med 1, Ulm, Germany
关键词
AGE-RELATED-CHANGES; PROGENITOR CELLS; SUBTYPES; BIOLOGY; LEUKEMOGENESIS; DYSREGULATION; HETEROGENEITY; MOBILIZATION; COMPARTMENT; SENESCENCE;
D O I
10.1016/j.coi.2014.05.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aging is organized in a hierarchy, in which aging of cells results in aged tissues, ultimately limiting lifespan. For organ systems that also in the adult depend on stem cells for tissue homeostasis like the hematopoietic system that forms immune cells, it is believed that aging of the stem cells strongly contributes to aging-associated dysfunction. In this review, we summarize current aspects on cellular and molecular mechanisms that are associated with aging of hematopoietic stem cells, the role of the stem cell niche for stem cell aging as well as novel and encouraging experimental approaches to attenuate aging of hematopoietic stem cells to target immunosenescence.
引用
收藏
页码:86 / 92
页数:7
相关论文
共 80 条
[1]   Functionally distinct hematopoietic stem cells modulate hematopoietic lineage potential during aging by a mechanism of clonal expansion [J].
Beerman, Isabel ;
Bhattacharya, Deepta ;
Zandi, Sasan ;
Sigvardsson, Mikael ;
Weissman, Irving L. ;
Bryder, David ;
Rossi, Derrick J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (12) :5465-5470
[2]   Hematopoietic Stem Cell Subtypes Expand Differentially during Development and Display Distinct Lymphopoietic Programs [J].
Benz, Claudia ;
Copley, Michael R. ;
Kent, David G. ;
Wohrer, Stefan ;
Cortes, Adrian ;
Aghaeepour, Nima ;
Ma, Elaine ;
Mader, Heidi ;
Rowe, Keegan ;
Day, Christopher ;
Treloar, David ;
Brinkman, Ryan R. ;
Eaves, Connie J. .
CELL STEM CELL, 2012, 10 (03) :273-283
[3]  
Berliner Nancy, 2013, Trans Am Clin Climatol Assoc, V124, P230
[4]   Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis [J].
Brack, Andrew S. ;
Conboy, Michael J. ;
Roy, Sudeep ;
Lee, Mark ;
Kuo, Calvin J. ;
Keller, Charles ;
Rando, Thomas A. .
SCIENCE, 2007, 317 (5839) :807-810
[5]   SIRT3 Reverses Aging-Associated Degeneration [J].
Brown, Katharine ;
Xie, Stephanie ;
Qiu, Xiaolei ;
Mohrin, Mary ;
Shin, Jiyung ;
Liu, Yufei ;
Zhang, Dan ;
Scadden, David T. ;
Chen, Danica .
CELL REPORTS, 2013, 3 (02) :319-327
[6]   A systems biology approach to Down syndrome: Identification of Notch/Wnt dysregulation in a model of stem cells aging [J].
Cairney, C. J. ;
Sanguinetti, G. ;
Ranghini, E. ;
Chantry, A. D. ;
Nostro, M. C. ;
Bhattacharya, A. ;
Svendsen, C. N. ;
Keith, W. N. ;
Bellantuono, I. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2009, 1792 (04) :353-363
[7]   Distinct Hematopoietic Stem Cell Subtypes Are Differentially Regulated by TGF-β1 [J].
Challen, Grant A. ;
Boles, Nathan C. ;
Chambers, Stuart M. ;
Goodell, Margaret A. .
CELL STEM CELL, 2010, 6 (03) :265-278
[8]   Aging hematopoietic stem cells decline in function and exhibit epigenetic dysregulation [J].
Chambers, Stuart M. ;
Shaw, Chad A. ;
Gatza, Catherine ;
Fisk, C. Joseph ;
Donehower, Lawrence A. ;
Goodell, Margaret A. .
PLOS BIOLOGY, 2007, 5 (08) :1750-1762
[9]   Genetic regulation of primitive hematopoietic stem cell senescence [J].
Chen, JC ;
Astle, CM ;
Harrison, DE .
EXPERIMENTAL HEMATOLOGY, 2000, 28 (04) :442-450
[10]   Hematopoietic senescence is postponed and hematopoietic stem cell function is enhanced by dietary restriction [J].
Chen, JC ;
Astle, CM ;
Harrison, DE .
EXPERIMENTAL HEMATOLOGY, 2003, 31 (11) :1097-1103