Prolonged expression of c-fos suppresses cell cycle entry of dormant hematopoietic stem cells

被引:39
作者
Okada, S [1 ]
Fukuda, T [1 ]
Inada, K [1 ]
Tokuhisa, T [1 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Dev Genet, Chiba 2608670, Japan
关键词
D O I
10.1182/blood.V93.3.816.403k21_816_825
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The proto-oncogene c-fos was transiently upregulated in primitive hematopoietic stem (Lin(-)Sca-1(+)) cells stimulated with stem cell factor, interleukin-3 (IL-3), and IL-6, To investigate a role of the c-fos in hematopoietic stem cells, we used bone marrow (BM) cells from transgenic mice carrying the c-fos gene under the control of the interferon-alpha/beta-inducible Mx-promoter (Mx-c-fos), and fetal liver cells from c-fos-deficient mice, Prolonged expression of the c-fos in Lin(-)Sca-1(+) BM cells inhibited factor-dependent colony formation and hematopoiesis on a stromal cell layer by keeping them at G0/G1 phase of the cell cycle. These Lin(-)Sca-1(+) BM cells on a stromal layer entered into the cell cycle whenever exogenous c-fos was downregulated. However, ectopic c-fos did not perturb colony formation by Lin(-)Sca-1(+) BM cells after they entered the cell cycle. Furthermore, endogenous c-fos is not essential to cell cycle progression of hematopoietic stem cells because the factor-dependent and the stroma-dependent hematopoiesis by Lin(-)Sca-1(+) fetal liver cells from c-fos-deficient mice was not impaired. These results suggest that the c-fos induced in primitive hematopoietic stem cells negatively controls cell cycle progression and maintains them in a dormant state. (C) 1999 by The American Society of Hematology.
引用
收藏
页码:816 / 825
页数:10
相关论文
共 60 条
[11]  
Hu L, 1996, J IMMUNOL, V157, P3804
[12]   GRANULOCYTE COLONY-STIMULATING FACTOR ENHANCES INTERLEUKIN-3-DEPENDENT PROLIFERATION OF MULTIPOTENTIAL HEMATOPOIETIC PROGENITORS [J].
IKEBUCHI, K ;
CLARK, SC ;
IHLE, JN ;
SOUZA, LM ;
OGAWA, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (10) :3445-3449
[13]  
Inada K, 1998, J IMMUNOL, V161, P3853
[14]   ERYTHROID COLONY FORMATION IN CULTURES OF MOUSE AND HUMAN BONE-MARROW - ANALYSIS OF REQUIREMENT FOR ERYTHROPOIETIN BY GEL-FILTRATION AND AFFINITY CHROMATOGRAPHY ON AGAROSE-CONCANAVALIN-A [J].
ISCOVE, NN ;
SIEBER, F ;
WINTERHALTER, KH .
JOURNAL OF CELLULAR PHYSIOLOGY, 1974, 83 (02) :309-320
[15]   NORMAL PERIPHERAL T-CELL FUNCTION IN C-FOS-DEFICIENT MICE [J].
JAIN, JN ;
NALEFSKI, EA ;
MCCAFFREY, PG ;
JOHNSON, RS ;
SPIEGELMAN, BM ;
PAPAIOANNOU, V ;
RAO, A .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :1566-1574
[16]   PLEIOTROPIC EFFECTS OF A NULL MUTATION IN THE C-FOS PROTOONCOGENE [J].
JOHNSON, RS ;
SPIEGELMAN, BM ;
PAPAIOANNOU, V .
CELL, 1992, 71 (04) :577-586
[17]   CLONAL AND SYSTEMIC ANALYSIS OF LONG-TERM HEMATOPOIESIS IN THE MOUSE [J].
JORDAN, CT ;
LEMISCHKA, IR .
GENES & DEVELOPMENT, 1990, 4 (02) :220-232
[18]   AP-1 function and regulation [J].
Karin, M ;
Liu, ZG ;
Zandi, E .
CURRENT OPINION IN CELL BIOLOGY, 1997, 9 (02) :240-246
[19]  
KATAYAMA N, 1993, BLOOD, V81, P610
[20]  
Kobayashi K, 1997, J IMMUNOL, V158, P2050