Cell differentiation and proliferation - Simultaneous but independent?

被引:63
作者
Brown, G
Hughes, PJ
Michell, RH
机构
[1] Univ Birmingham, Sch Med, Div Immun & Infect, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
关键词
CYCLIN-DEPENDENT KINASES; GROWTH-FACTOR-I; 1,25-DIHYDROXYVITAMIN D-3-INDUCED DIFFERENTIATION; HEAVY-CHAIN SWITCH; T-CELL; HL60; CELLS; GENE-EXPRESSION; CLONAL EXPANSION; MICE LACKING; PREADIPOCYTE DIFFERENTIATION;
D O I
10.1016/S0014-4827(03)00393-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite studies over many years, it is still not clear to what extent cellular controls on proliferation and on differentiation are interrelated. For example, the idea that exit from cell cycle into G1/G0 is a necessary-or at least frequent-prelude to differentiation developed partly from studies of haemopoietic cell maturation, often using cell lines as models. The responses of cells to treatment with differentiating agents suggested that exit from cell cycle into G1/G0 occurs quite quickly, with functional differentiated characteristics acquired later, and so promoted the notion that cyclin-dependent kinase inhibitors (CDKIs) might be important initiators of normal differentiation. However, recent work has made it clear that differentiation and cell proliferation are regulated simultaneously but independently, that cells often start differentiating long before they stop dividing, and that the launching of differentiation is not restricted to any particular segment of the cell cycle. This combination of attributes allows expansion of cell numbers and acquisition of differentiated function to occur in parallel, generating abundant effector cells. Given this dichotomy, future studies to develop a more exact picture of the events that initiate and drive differentiation might be simplified by studying differentiation under experimental conditions that divorce it from concerns about cell cycle control. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:282 / 288
页数:7
相关论文
共 72 条
[31]   New functional activities for the p21 family of CDK inhibitors [J].
LaBaer, J ;
Garrett, MD ;
Stevenson, LF ;
Slingerland, JM ;
Sandhu, C ;
Chou, HS ;
Fattaey, A ;
Harlow, E .
GENES & DEVELOPMENT, 1997, 11 (07) :847-862
[32]   Functional flexibility in T cells:: Independent regulation of CD4+ T cell proliferation and effector function in vivo [J].
Laouar, Y ;
Crispe, IN .
IMMUNITY, 2000, 13 (03) :291-301
[33]   Commitment point during G0→G1 that controls entry into the cell cycle [J].
Lea, NC ;
Orr, SJ ;
Stoeber, K ;
Williams, GH ;
Lam, EWF ;
Ibrahim, MAA ;
Mufti, GJ ;
Thomas, NSB .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (07) :2351-2361
[34]   CYCLIN-DEPENDENT KINASE REGULATION [J].
LEES, E .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (06) :773-780
[35]   Regulation of myeloid growth and differentiation by the insulin-like growth factor I receptor [J].
Li, YM ;
Schacher, DH ;
Liu, Q ;
Arkins, S ;
Rebeiz, N ;
McCusker, RH ;
Dantzer, R ;
Kelley, KW .
ENDOCRINOLOGY, 1997, 138 (01) :362-368
[36]   THE BLOCKADE OF PREADIPOCYTE DIFFERENTIATION BY PROTEIN-TYROSINE-PHOSPHATASE HA2 IS REVERSED BY VANADATE [J].
LIAO, K ;
LANE, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (20) :12123-12132
[37]   Transcriptional activation of the Cdk inhibitor p21 by vitamin D-3 leads to the induced differentiation of the myelomonocytic cell line U937 [J].
Liu, M ;
Lee, MH ;
Cohen, M ;
Bommakanti, M ;
Freedman, LP .
GENES & DEVELOPMENT, 1996, 10 (02) :142-153
[38]  
Liu Q, 1999, MOL CELL BIOL, V19, P6229
[39]  
Liu Q, 1998, J IMMUNOL, V160, P1393
[40]   Gene expression networks underlying retinoic acid-induced differentiation of acute promyelocytic leukemia cells [J].
Liu, TX ;
Zhang, JW ;
Tao, J ;
Zhang, RB ;
Zhang, QH ;
Zhao, CJ ;
Tong, JH ;
Lanotte, M ;
Waxman, S ;
Chen, SJ ;
Mao, M ;
Hu, GX ;
Zhu, L ;
Chen, Z .
BLOOD, 2000, 96 (04) :1496-1504