Mechanisms of Stem Cell Self-Renewal

被引:401
作者
He, Shenghui [1 ]
Nakada, Daisuke [1 ]
Morrison, Sean J. [1 ]
机构
[1] Univ Michigan, Howard Hughes Med Inst, Inst Life Sci, Dept Internal Med,Ctr Stem Cell Biol, Ann Arbor, MI 48109 USA
关键词
cell cycle; niche; tumor suppressor; oncogene; aging; cancer; TRANSCRIPTIONAL REGULATORY CIRCUITRY; NEURAL PROGENITOR CELLS; HEMATOPOIETIC STEM; TUMOR-SUPPRESSOR; LONG-TERM; DEPENDENCE DISTINGUISHES; LIFE-SPAN; DEVELOPMENTAL REGULATORS; SUBVENTRICULAR ZONE; MOUSE DEVELOPMENT;
D O I
10.1146/annurev.cellbio.042308.113248
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Self-renewal is the process by which stem cells divide to make more stein cells, perpetuating die stem cell pool throughout life. Self-renewal is division with maintenance of the undifferentiated state. This requires cell cycle control and often maintenance of multipotency or pluripotency, depending on the stem cell. Self-renewal programs involve networks that balance proto-oncogenes (promoting self-renewal), gate-keeping tumor suppressors (limiting self-renewal), and care-taking tumor suppressors (maintaining genomic integrity). These cell-intrinsic mechanisms are regulated by cell-extrinsic signals from the niche, the microenvironment that maintains stein cells and regulates their function in tissues. In response to changing tissue demands, stem cells undergo changes in cell cycle status and developmental potential over time, requiring different self-renewal programs at different stages of life. Reduced stem cell function and tissue regenerative capacity during aging are caused by changes in self-renewal programs that augment tumor suppression. Cancer arises from mutations that inappropriately activate self-renewal programs.
引用
收藏
页码:377 / 406
页数:30
相关论文
共 194 条
  • [1] Long-term haematopoietic reconstitution by Trp53-/-p16Ink4a-/-p19Arf-/- multipotent progenitors
    Akala, Omobolaji O.
    Park, In-Kyung
    Qian, Dalong
    Pihalja, Michael
    Becker, Michael W.
    Clarke, Michael F.
    [J]. NATURE, 2008, 453 (7192) : 228 - U12
  • [2] ES cells do not activate p53-dependent stress responses and undergo p53-independent apoptosis in response to DNA damage
    Aladjem, MI
    Spike, BT
    Rodewald, LW
    Hope, TJ
    Klemm, M
    Jaenisch, R
    Wahl, GM
    [J]. CURRENT BIOLOGY, 1998, 8 (03) : 145 - 155
  • [3] Ataxia telangiectasia mutated is essential during adult neurogenesis
    Allen, DR
    van Praag, H
    Ray, J
    Weaver, Z
    Winrow, CJ
    Carter, TA
    Braquet, R
    Harrington, E
    Ried, T
    Brown, KD
    Gage, FH
    Barlow, C
    [J]. GENES & DEVELOPMENT, 2001, 15 (05) : 554 - 566
  • [4] Telomerase is required to slow telomere shortening and extend replicative lifespan of HSCs during serial transplantation
    Allsopp, RC
    Morin, GB
    DePinho, R
    Harley, CB
    Weissman, IL
    [J]. BLOOD, 2003, 102 (02) : 517 - 520
  • [5] Gli and hedgehog in cancer:: Tumours, embryos and stem cells
    Altaba, AR
    Sánchez, P
    Dahmane, N
    [J]. NATURE REVIEWS CANCER, 2002, 2 (05) : 361 - 372
  • [6] Angelastro JM, 2003, J NEUROSCI, V23, P4590
  • [7] Downregulation of activating transcription factor 5 is required for differentiation of neural progenitor cells into astrocytes
    Angelastro, JM
    Mason, JL
    Ignatova, TN
    Kukekov, VG
    Stengren, GB
    Goldman, JE
    Greene, LA
    [J]. JOURNAL OF NEUROSCIENCE, 2005, 25 (15) : 3889 - 3899
  • [8] Tie2/angiopoietin-1 signaling regulates hematopoietic stem cell quiescence in the bone marrow niche
    Arai, F
    Hirao, A
    Ohmura, M
    Sato, H
    Matsuoka, S
    Takubo, K
    Ito, K
    Koh, GY
    Suda, T
    [J]. CELL, 2004, 118 (02) : 149 - 161
  • [9] Multipotent cell lineages in early mouse development depend on SOX2 function
    Avilion, AA
    Nicolis, SK
    Pevny, LH
    Perez, L
    Vivian, N
    Lovell-Badge, R
    [J]. GENES & DEVELOPMENT, 2003, 17 (01) : 126 - 140
  • [10] Chromatin signatures of pluripotent cell lines
    Azuara, V
    Perry, P
    Sauer, S
    Spivakov, M
    Jorgensen, HF
    John, RM
    Gouti, M
    Casanova, M
    Warnes, G
    Merkenschlager, M
    Fisher, AG
    [J]. NATURE CELL BIOLOGY, 2006, 8 (05) : 532 - U189