BTK as a mediator of radiation-induced apoptosis in DT-40 lymphoma B cells

被引:160
作者
Uckun, FM
Waddick, KG
Mahajan, S
Jun, X
Takata, M
Bolen, J
Kurosaki, T
机构
[1] YALE UNIV,SCH MED,IMMUNOBIOL SECT,NEW HAVEN,CT 06510
[2] DNAX RES INST MOL & CELLULAR BIOL INC,PALO ALTO,CA 94304
关键词
D O I
10.1126/science.273.5278.1096
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
Bruton's tyrosine kinase (BTK) is a member of the SRC-related TEC family of protein tyrosine kinases (PTKs). DT-40 lymphoma B cells, rendered BTK-deficient through targeted disruption of the btk gene by homologous recombination knockout, did not undergo radiation-induced apoptosis, but cells with disrupted lyn or syk genes did. Introduction of the wild-type, or a SRC homology 2 domain or a plecstrin homology domain mutant (but not a kinase domain mutant), human btk gene into BTK-deficient cells restored the apoptotic response to radiation. Thus, BTK is the PTK responsible for triggering radiation-induced apoptosis of lymphoma B cells, and its kinase domain is indispensable for the apoptotic response.
引用
收藏
页码:1096 / 1100
页数:5
相关论文
共 78 条