Newman Rebecca, Turner Martin
Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Babraham Research Campus, CB22 3AT, Babraham, UK,
Adv Exp Med Biol. 2015;850:119-35. doi: 10.1007/978-3-319-15774-0_9.
The phosphatidylinositol-3-kinase (PI3K) pathway has an essential role in signal transduction, where it is required for a number of different cellular processes including proliferation, differentiation, development, migration and growth. In the immune system, PI3K regulates inflammation by controlling the activation and recruitment of leukocytes. The generation of conditional knockout mice has allowed the study of PI3K isoforms specifically in B and T lymphocytes, and demonstrates the importance of intact signalling in their development and function. PI3K signalling must be tightly regulated in lymphocytes as excessive PI3K can lead to autoimmunity, immunodeficiency or cancer, whilst diminished signalling can result in developmental defects and immunodeficiency. Recent advances in the understanding of PI3K signalling have hastened the application of isoform-specific PI3K inhibitors, which are currently undergoing clinical trials. This review will focus on the p110δ catalytic subunit of the class 1A family of PI3K, and its role in the development and activation of B lymphocytes through various downstream effectors.
磷脂酰肌醇-3-激酶(PI3K)信号通路在信号转导中起着至关重要的作用,许多不同的细胞过程都需要该通路,包括增殖、分化、发育、迁移和生长。在免疫系统中,PI3K通过控制白细胞的激活和募集来调节炎症。条件性基因敲除小鼠的产生使得能够专门研究B淋巴细胞和T淋巴细胞中的PI3K亚型,并证明了完整信号传导在其发育和功能中的重要性。PI3K信号在淋巴细胞中必须受到严格调控,因为PI3K过度激活会导致自身免疫、免疫缺陷或癌症,而信号减弱则会导致发育缺陷和免疫缺陷。对PI3K信号传导认识的最新进展加速了亚型特异性PI3K抑制剂的应用,这些抑制剂目前正在进行临床试验。本综述将聚焦于1A类PI3K家族的p110δ催化亚基,及其通过各种下游效应器在B淋巴细胞发育和激活中的作用。