Department of Molecular Biology and Biochemistry, Institute for Immunology, University of California Irvine Irvine, CA, USA.
Front Immunol. 2012 Aug 6;3:228. doi: 10.3389/fimmu.2012.00228. eCollection 2012.
Activation of phosphoinositide 3-kinase (PI3K) is required for B cell proliferation and survival. PI3K signaling also controls key aspects of B cell differentiation. Upon engagement of the B cell receptor (BCR), PI3K activation promotes Ca(2+) mobilization and activation of NFκB-dependent transcription, events which are essential for B cell proliferation. PI3K also initiates a distinct signaling pathway involving the Akt and mTOR serine/threonine kinases. It has been generally assumed that activation of Akt and mTOR downstream of PI3K is essential for B cell function. However, Akt and mTOR have complex roles in B cell fate decisions and suppression of this pathway can enhance certain B cell responses while repressing others. In this review we will discuss genetic and pharmacological studies of Akt and mTOR function in normal B cells, and in malignancies of B cell origin.
磷酸肌醇 3-激酶 (PI3K) 的激活对于 B 细胞的增殖和存活是必需的。PI3K 信号还控制 B 细胞分化的关键方面。在 B 细胞受体 (BCR) 结合后,PI3K 的激活促进 Ca(2+)动员和 NFκB 依赖性转录的激活,这些事件对于 B 细胞的增殖是必不可少的。PI3K 还启动了一条涉及 Akt 和 mTOR 丝氨酸/苏氨酸激酶的独特信号通路。通常认为,PI3K 下游 Akt 和 mTOR 的激活对于 B 细胞功能是必需的。然而,Akt 和 mTOR 在 B 细胞命运决定中具有复杂的作用,抑制该途径可以增强某些 B 细胞反应,同时抑制其他反应。在这篇综述中,我们将讨论 Akt 和 mTOR 在正常 B 细胞以及 B 细胞来源的恶性肿瘤中的功能的遗传和药理学研究。