Stat5: an essential regulator of mast cell biology

被引:25
作者
Shelburne, CP
McCoy, ME
Piekorz, R
Sexl, VV
Gillespie, SR
Bailey, DP
Gharse, A
Mirmonsef, P
Mann, MN
Kashyap, M
Wright, HV
Chong, HJ
Bouton, LA
Ramirez, CD
Lantz, CS
Ryan, JJ [1 ]
机构
[1] Virginia Commonwealth Univ, Dept Biol, Richmond, VA 23284 USA
[2] James Madison Univ, Dept Biol, Harrisonburg, VA 22807 USA
[3] St Jude Childrens Res Hosp, Dept Biochem, Memphis, TN 38105 USA
关键词
cytokine; interleukin-3; stem cell factor; c-kit; apoptosis;
D O I
10.1016/S0161-5890(02)00061-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin-3 (IL-3) and stem cell factor (SCF) are important mast cell growth and differentiation factors. Since both cytokines activate the transcription factor Stat5, a known regulator of proliferation and survival, we investigated the effects of Stat5 deficiency on mast cell development and survival. This article will review data presented at The Fourth International Workshop on Signal Transduction in the Activation and Development of Mast Cells and Basophils. The full set of data is now in preparation for publication. We find that the absence of Stat5 A and B results in a total loss of in vivo mast cell development. Bone marrow-derived mast cell (BMMC) populations can be cultured and maintained from Stat5-deficient mice in IL-3 + SCF, but not in either cytokine alone. The absence of Stat5 resulted in aberrant control of Bcl-2, Bcl-X-L and cyclin A2, with increased apoptosis and delayed cell cycle progression after IL-3 or SCF stimulation. These results indicate that Stat5 A and B are critical regulators of in vitro and in vivo mast cell biology. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1187 / 1191
页数:5
相关论文
共 26 条
[1]   Mast cell lineage development and phenotypic regulation [J].
Austen, KF ;
Boyce, JA .
LEUKEMIA RESEARCH, 2001, 25 (07) :511-518
[2]   STAT protein recruitment and activation in c-Kit deletion mutants [J].
Brizzi, MF ;
Dentelli, P ;
Rosso, A ;
Yarden, Y ;
Pegoraro, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (24) :16965-16972
[3]  
de Groot Rolf P., 2000, Molecular Cell Biology Research Communications, V3, P299, DOI 10.1006/mcbr.2000.0231
[4]  
Galli S J, 1994, Curr Opin Hematol, V1, P33
[5]   Bcr/Abl activates transcription of the Bcl-X gene through STAT5 [J].
Gesbert, F ;
Griffin, JD .
BLOOD, 2000, 96 (06) :2269-2276
[6]   Protection from apoptosis by steel factor but not interleukin-3 is reversed through blockade of calcium influx [J].
Gommerman, JL ;
Berger, SA .
BLOOD, 1998, 91 (06) :1891-1900
[7]   Dominant negative mutants implicate STAT5 in myeloid cell proliferation and neutrophil differentiation [J].
Ilaria, RL ;
Hawley, RG ;
Van Etten, RA .
BLOOD, 1999, 93 (12) :4154-4166
[8]   MAST-CELLS IN SKIN OF NORMAL, HAIRLESS AND ATHYMIC MICE [J].
KELLER, R ;
HESS, MW ;
RILEY, JF .
EXPERIENTIA, 1976, 32 (02) :171-172
[9]   Role for interleukin-3 in mast-cell and basophil development and in immunity to parasites [J].
Lantz, CS ;
Boesiger, J ;
Song, CH ;
Mach, N ;
Kobayashi, T ;
Mulligan, RC ;
Nawa, Y ;
Dranoff, G ;
Galli, SJ .
NATURE, 1998, 392 (6671) :90-93
[10]   JAKS AND STATS: Biological implications [J].
Leonard, WJ ;
O'Shea, JJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1998, 16 :293-322