Pouillon Valérie, Hascakova-Bartova Romana, Pajak Bernard, Adam Emmanuelle, Bex Françoise, Dewaste Valérie, Van Lint Carine, Leo Oberdan, Erneux Christophe, Schurmans Stéphane
IRIBHM, IBMM, rue des Professeurs Jeener et Brachet 12, 6041 Gosselies, Belgium.
Nat Immunol. 2003 Nov;4(11):1136-43. doi: 10.1038/ni980. Epub 2003 Sep 28.
Inositol 1,4,5-trisphosphate (Ins(1,4,5)P(3)) is phosphorylated by Ins(1,4,5)P(3) 3-kinase, generating inositol 1,3,4,5-tetrakisphosphate (Ins(1,3,4,5)P(4)). The physiological function of Ins(1,3,4,5)P(4) is still unclear, but it has been reported to be a potential modulator of calcium mobilization. Disruption of the gene encoding the ubiquitously expressed Ins(1,4,5)P(3) 3-kinase isoform B (Itpkb) in mice caused a severe T cell deficiency due to major alterations in thymocyte responsiveness and selection. However, we were unable to detect substantial defects in Ins(1,4,5)P(3) amounts or calcium mobilization in Itpkb(-/-) thymocytes. These data indicate that Itpkb and Ins(1,3,4,5)P(4) define an essential signaling pathway for T cell precursor responsiveness and development.
肌醇1,4,5-三磷酸(Ins(1,4,5)P(3))被肌醇1,4,5-三磷酸3-激酶磷酸化,生成肌醇1,3,4,5-四磷酸(Ins(1,3,4,5)P(4))。Ins(1,3,4,5)P(4)的生理功能仍不清楚,但据报道它是钙动员的潜在调节因子。小鼠中编码普遍表达的肌醇1,4,5-三磷酸3-激酶同工型B(Itpkb)的基因破坏,由于胸腺细胞反应性和选择的重大改变,导致严重的T细胞缺陷。然而,我们未能在Itpkb(-/-)胸腺细胞中检测到Ins(1,4,5)P(3)量或钙动员的实质性缺陷。这些数据表明,Itpkb和Ins(1,3,4,5)P(4)定义了T细胞前体反应性和发育的重要信号通路。