CD19 OF B-CELLS AS A SURROGATE KINASE INSERT REGION TO BIND PHOSPHATIDYLINOSITOL 3-KINASE

被引:299
作者
TUVESON, DA
CARTER, RH
SOLTOFF, SP
FEARON, DT
机构
[1] JOHNS HOPKINS UNIV, SCH MED, DEPT MED, BALTIMORE, MD 21205 USA
[2] HARVARD UNIV, BETH ISRAEL HOSP,SCH MED,DEPT MED, DIV SIGNAL TRANSDUCT, BOSTON, MA 02215 USA
关键词
D O I
10.1126/science.7684160
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
Antigen receptors on B and T lymphocytes transduce signals by activating nonreceptor protein tyrosine kinases (PTKs). A family of receptor PTKs contains kinase insert regions with the sequence tyrosine-X-X-methionine (where X is any amino acid) that when phosphorylated mediate the binding and activation of phosphatidylinositol 3-kinase (PI 3-kinase). The CD19 membrane protein of B cells enhances activation through membrane immunoglobulin M (mIgM) and was found to contain a functional analog of the kinase insert region. Ligation of mIgM induced phosphorylation of CD19 and association with PI 3-kinase. Thus, CD19 serves as a surrogate kinase insert region for mIgM by providing the means for PI 3-kinase activation by nonreceptor PTKs.
引用
收藏
页码:986 / 989
页数:4
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