PROFOUND BLOCK IN THYMOCYTE DEVELOPMENT IN MICE LACKING P56(LCK)

被引:951
作者
MOLINA, TJ
KISHIHARA, K
SIDEROVSKI, DP
VANEWIJK, W
NARENDRAN, A
TIMMS, E
WAKEHAM, A
PAIGE, CJ
HARTMANN, KU
VEILLETTE, A
DAVIDSON, D
MAK, TW
机构
[1] UNIV TORONTO, ONTARIO CANC INST, 500 SHERBOURNE ST, TORONTO M4X 1K9, ONTARIO, CANADA
[2] UNIV TORONTO, DEPT IMMUNOL, TORONTO M4X 1K9, ONTARIO, CANADA
[3] UNIV TORONTO, DEPT MED BIOPHYS, TORONTO M4X 1K9, ONTARIO, CANADA
[4] ERASMUS UNIV, DEPT CELL BIOL & IMMUNOL 2, 3000 DR ROTTERDAM, NETHERLANDS
[5] UNIV MARBURG, INST EXPTL IMMUNOL, W-3550 MARBURG, GERMANY
[6] MCGILL UNIV, CTR CANC, MONTREAL H3G 1Y6, QUEBEC, CANADA
关键词
D O I
10.1038/357161a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
THE protein Lck (p56lck) has a relative molecular mass of 56,000 and belongs to the Src family of tyrosine kinases 1-3. It is expressed exclusively in lymphoid cells, predominantly in thymocytes and peripheral T cells 4-5. Lck associates specifically with the cytoplasmic domains of both CD4 and CD8 T-cell surface glycoproteins 6,7 and interacts with the beta-chain of the interleukin-2 receptor 8, which implicates Lck activity in signal transduction during thymocyte ontogeny 9-13 and activation of mature T cells 14-19. Here we generate an lck null mutation by homologous recombination in embryonic stem cells to evaluate the role of p56lck in T-cell development and activation. Lck-deficient mice show a pronounced thymic atrophy, with a dramatic reduction in the double-positive (CD4+CD8+) thymocyte population. Mature, single-positive thymocytes are not detectable in these mice and there are only very few peripheral T cells. These results illustrate the crucial role of this T-cell-specific tyrosine kinase in the thymocyte development.
引用
收藏
页码:161 / 164
页数:4
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