Miller Andrew T, Beisner Daniel R, Liu Daorong, Cooke Michael P
The Genomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
J Immunol. 2009 Apr 15;182(8):4696-704. doi: 10.4049/jimmunol.0802850.
Inositol 1,4,5-trisphosphate 3-kinase B (or Itpkb) converts inositol 1,4,5-trisphosphate to inositol 1,3,4,5-tetrakisphosphate upon Ag receptor activation and controls the fate and function of lymphocytes. To determine the role of Itpkb in B cell tolerance, Itpkb(-/-) mice were crossed to transgenic mice that express a BCR specific for hen egg lysozyme (IgHEL). B cells from Itpkb(-/-) IgHEL mice possess an anergic phenotype, hypoproliferate in response to cognate Ag, and yet they exhibit enhanced Ag-induced calcium signaling. In IgHEL transgenic mice that also express soluble HEL, lack of Itpkb converts anergy induction to deletion. These data establish Itpkb as a negative regulator of BCR signaling that controls the fate of developing B cells and tolerance induction.
肌醇1,4,5-三磷酸3-激酶B(或Itpkb)在抗原受体激活后将肌醇1,4,5-三磷酸转化为肌醇1,3,4,5-四磷酸,并控制淋巴细胞的命运和功能。为了确定Itpkb在B细胞耐受性中的作用,将Itpkb基因敲除小鼠与表达针对鸡卵溶菌酶的BCR(IgHEL)的转基因小鼠进行杂交。来自Itpkb基因敲除IgHEL小鼠的B细胞具有无反应性表型,对同源抗原反应性增殖低下,但它们表现出增强的抗原诱导的钙信号传导。在也表达可溶性HEL的IgHEL转基因小鼠中,缺乏Itpkb会将无反应性诱导转变为细胞清除。这些数据确立了Itpkb作为BCR信号传导的负调节因子,其控制发育中B细胞的命运和耐受性诱导。