DIFFERENTIAL-EFFECTS OF BCL-2 ON T-CELLS AND B-CELLS IN TRANSGENIC MICE

被引:123
作者
KATSUMATA, M [1 ]
SIEGEL, RM [1 ]
LOUIE, DC [1 ]
MIYASHITA, T [1 ]
TSUJIMOTO, Y [1 ]
NOWELL, PC [1 ]
GREENE, MI [1 ]
REED, JC [1 ]
机构
[1] WISTAR INST,PHILADELPHIA,PA 19104
关键词
GENETICS OF LYMPHOMA; APOPTOSIS; T-CELL DEVELOPMENT; T-CELL SUBSETS; ONCOGENE;
D O I
10.1073/pnas.89.23.11376
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
We have produced bcl-2 transgenic mice by using a construct which mimics the t(14;18) translocation in human follicular lymphomas. Although lymphoid tissues from all transgenic mice contained high levels of human Bcl-2 protein, transgene expression was differentially regulated within the B- and T-cell compartments of lines derived from various founder mice. We have characterized the phenotypes of two lines of bcl-2 transgenic mice (line 2 and line 6) in which bcl-2 transgene expression was restricted primarily to the T- or B-cell lineages, respectively. Analysis of line 6 lymphocytes revealed a polyclonal expansion of B cells, and these B cells exhibited prolonged survival in vitro. In line 2 mice, numbers of T cells in the peripheral lymphoid tissues were more moderately elevated despite enhanced T-cell survival in vitro. Line 2 transgenic mice also showed significantly increased proportions of thymocytes with a mature phenotype. Taken together, these findings suggest different roles for bcl-2 in the in vivo regulation of B- and T-cell development and homeostasis.
引用
收藏
页码:11376 / 11380
页数:5
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