Fruman D A
Department of Molecular Biology and Biochemistry and Center for Immunology, University of California, Irvine, CA 92697, USA.
Biochem Soc Trans. 2007 Apr;35(Pt 2):177-80. doi: 10.1042/BST0350177.
PI3K (phosphoinositide 3-kinase) regulates diverse cellular responses in the immune system, and members of this enzyme family are considered attractive drug targets for modulating allergy, inflammation and leukaemia. Clearly it is important to understand the function of PI3K in T-lymphocytes, cells that regulate nearly every aspect of immunity. However, the precise role of PI3K in T-cell development and function has been difficult to determine. In this review, I summarize current knowledge of PI3K function in T-cells, focusing on the class I subgroup of PI3K catalytic and regulatory isoforms. I discuss gene disruption studies in mice that reveal redundant or limited roles for individual isoforms, along with evidence for potential autoimmunity when class IA PI3K signalling is reduced.
磷脂酰肌醇-3激酶(PI3K)调节免疫系统中的多种细胞反应,该酶家族成员被认为是调节过敏、炎症和白血病的有吸引力的药物靶点。显然,了解PI3K在T淋巴细胞(几乎调节免疫各个方面的细胞)中的功能非常重要。然而,PI3K在T细胞发育和功能中的精确作用一直难以确定。在这篇综述中,我总结了目前关于PI3K在T细胞中功能的知识,重点关注PI3K催化和调节亚型的I类亚组。我讨论了小鼠中的基因敲除研究,这些研究揭示了单个亚型的冗余或有限作用,以及IA类PI3K信号减少时潜在自身免疫的证据。