DISAPPEARANCE OF THE LYMPHOID SYSTEM IN BCL-2 HOMOZYGOUS MUTANT CHIMERIC MICE

被引:384
作者
NAKAYAMA, K
NAKAYAMA, K
NEGISHI, I
KUIDA, K
SHINKAI, Y
LOUIE, MC
FIELDS, LE
LUCAS, PJ
STEWART, V
ALT, FW
LOH, DY
机构
[1] WASHINGTON UNIV, SCH MED, DEPT MED, HOWARD HUGHES MED INST, ST LOUIS, MO 63110 USA
[2] WASHINGTON UNIV, SCH MED, DEPT GENET, ST LOUIS, MO 63110 USA
[3] WASHINGTON UNIV, SCH MED, DEPT MOLEC MICROBIOL, ST LOUIS, MO 63110 USA
[4] HARVARD UNIV, CHILDRENS HOSP,SCH MED,DEPT GENET, HOWARD HUGHES MED INST, BOSTON, MA 02115 USA
[5] CTR BLOOD RES, BOSTON, MA 02115 USA
关键词
D O I
10.1126/science.8372353
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 bcl-2 proto-oncogene can prevent the death of many cell types. Mice were generated that were chimeric for the homozygous inactivation of bcl-2. Lymphocytes without Bcl-2 differentiated into phenotypically mature cells. However, in vitro, the mature T cells that lacked Bcl-2 had shorter life-spans and increased sensitivity to glucocorticoids and gamma-irradiation. In contrast, stimulation of CD3 inhibited the death of these cells. T and B cells with no Bcl-2 disappeared from the bone marrow, thymus, and periphery by 4 weeks of age. Thus, Bcl-2 was dispensable for lymphocyte maturation, but was required for a stable immune system after birth.
引用
收藏
页码:1584 / 1588
页数:5
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