Satterthwaite A B, Cheroutre H, Khan W N, Sideras P, Witte O N
Department of Microbiology and Molecular Genetics, University of California, Los Angeles 90095, USA.
Proc Natl Acad Sci U S A. 1997 Nov 25;94(24):13152-7. doi: 10.1073/pnas.94.24.13152.
Mutations in Btk result in the B cell immunodeficiencies X-linked agammaglobulinemia (XLA) in humans and X-linked immunodeficiency (xid) in mice. Btk is a critical component of signaling pathways regulating B cell development and function. We used a genetic approach to determine whether Btk is also limiting for these processes. One allele of a murine Btk transgene expressed a dosage of Btk (25% of endogenous levels in splenic B cells) sufficient to restore normal numbers of phenotypically mature conventional B cells in xid mice. 2,4,6-trinitrophenyl-Ficoll response, anti-IgM-induced proliferation, B1 cell development, and serum IgM and IgG3 levels remained significantly impaired in these animals. B cells from Btk -/- transgenic mice also responded poorly to anti-IgM, indicating that the xid mutation does not create a dominant negative form of Btk. Response to 2,4,6-trinitrophenyl-Ficoll and B cell receptor cross-linking were increased 3- to 4-fold in xid mice homozygous for the transgene. These results demonstrate that Btk is a limiting component of B cell antigen receptor signaling pathways and suggest that B cell development and response to antigen may require different levels of Btk activity.
布鲁顿酪氨酸激酶(Btk)的突变会导致人类的B细胞免疫缺陷——X连锁无丙种球蛋白血症(XLA)以及小鼠的X连锁免疫缺陷(xid)。Btk是调节B细胞发育和功能的信号通路的关键组成部分。我们采用遗传学方法来确定Btk是否也是这些过程的限制因素。一个小鼠Btk转基因的一个等位基因表达的Btk剂量(脾B细胞中内源性水平的25%)足以恢复xid小鼠中表型成熟的常规B细胞的正常数量。在这些动物中,2,4,6-三硝基苯-Ficoll反应、抗IgM诱导的增殖、B1细胞发育以及血清IgM和IgG3水平仍然显著受损。来自Btk -/-转基因小鼠的B细胞对抗IgM的反应也很差,这表明xid突变不会产生Btk的显性负性形式。对于转基因纯合的xid小鼠,对2,4,6-三硝基苯-Ficoll的反应和B细胞受体交联增加了3至4倍。这些结果表明,Btk是B细胞抗原受体信号通路的限制成分,并提示B细胞发育和对抗原的反应可能需要不同水平的Btk活性。