Telomeres, senescence, and hematopoietic stem cells

被引:39
作者
Zimmermann, Stefan [1 ]
Martens, Uwe M. [1 ]
机构
[1] Univ Freiburg, Med Ctr, Dept Hematol Oncol, D-79106 Freiburg, Germany
关键词
senescence; aging; telomerase; telomere; stem cells;
D O I
10.1007/s00441-007-0469-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The replicative lifespan of normal somatic cells is restricted by the erosion of telomeres, which are protective caps at the ends of linear chromosomes. The loss of telomeres induces antiproliferative signals that eventually lead to cellular senescence. The enzyme complex telomerase can maintain telomeres, but its expression is confined to highly proliferative cells such as stem cells and tumor cells. The immense regenerative capacity of the hematopoietic system is provided by a distinct type of adult stem cell: hematopoietic stem cells (HSCs). Although blood cells have to be produced continuously throughout life, the HSC pool seems not to be spared by aging processes. Indeed, limited expression of telomerase is not sufficient to prevent telomere shortening in these cells, which is thought ultimately to limit their proliferative capacity. In this review, we discuss the relevance of telomere maintenance for the hematopoietic stem cell compartment and consider potential functions of telomerase in this context. We also present possible clinical applications of telomere manipulation in HSCs and new insights affecting the aging of the hematopoietic stem cell pool and replicative exhaustion.
引用
收藏
页码:79 / 90
页数:12
相关论文
共 50 条
  • [41] Oxidized low-density lipoprotein induces hematopoietic stem cell senescence
    Zhang, Xian-Ping
    Zhang, Gui-Hai
    Wang, Yu-Ying
    Liu, Jun
    Wei, Qiang
    Xu, Chun-Yan
    Wang, Jian-Wei
    Wang, Ya-Ping
    CELL BIOLOGY INTERNATIONAL, 2013, 37 (09) : 940 - 948
  • [42] Feline chronic kidney disease is associated with shortened telomeres and increased cellular senescence
    Quimby, Jessica M.
    Maranon, David G.
    Battaglia, Christine L. R.
    McLeland, Shannon M.
    Brock, William T.
    Bailey, Susan M.
    AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2013, 305 (03) : F295 - F303
  • [43] Telomeres: the role of shortening and senescence in major depressive disorder and its therapeutic implications
    Schroder, Jessica Daniela
    de Araujo, Julia Beatrice
    de Oliveira, Tacio
    de Moura, Airam Barbosa
    Fries, Gabriel Rodrigo
    Quevedo, Joao
    Reus, Gislaine Zilli
    Ignacio, Zuleide Maria
    REVIEWS IN THE NEUROSCIENCES, 2022, 33 (03) : 227 - 255
  • [44] Mitochondria, telomeres and cell senescence
    Passos, JF
    von Zglinicki, T
    EXPERIMENTAL GERONTOLOGY, 2005, 40 (06) : 466 - 472
  • [45] Simulated shortening of proliferation-restricting telomeres during clonal proliferation and senescence of human cells
    Tan, Z
    EXPERIMENTAL GERONTOLOGY, 2001, 36 (01) : 89 - 97
  • [46] Hematopoietic stem cells and hematopoietic neoplasias
    Wickenhauser, C
    PATHOLOGE, 2002, 23 (06): : 457 - 464
  • [47] Telomeres,cardiovascular aging,and potential intervention for cellular senescence
    ZHANG WeiLi
    HUI RuTai
    YANG ShuJun
    Science China(Life Sciences), 2014, 57 (08) : 858 - 862
  • [48] Concise review: Telomere biology in normal and leukemic hematopoietic stem cells
    Drummond, Mark W.
    Balabanov, Stefan
    Holyoake, Tessa L.
    Brummendorf, Tim H.
    STEM CELLS, 2007, 25 (08) : 1853 - 1861
  • [49] Telomeres, cardiovascular aging, and potential intervention for cellular senescence
    Zhang WeiLi
    Hui RuTai
    Yang ShuJun
    SCIENCE CHINA-LIFE SCIENCES, 2014, 57 (08) : 858 - 862
  • [50] Telomeres, cardiovascular aging, and potential intervention for cellular senescence
    WeiLi Zhang
    RuTai Hui
    ShuJun Yang
    Science China Life Sciences, 2014, 57 : 858 - 862