Oak J S, Matheu M P, Parker I, Cahalan M D, Fruman D A
Center for Immunology, University of California, Irvine, Irvine, CA 92697, U.S.A.
Biochem Soc Trans. 2007 Nov;35(Pt 5):1109-13. doi: 10.1042/BST0351109.
The PI3K (phosphoinositide 3-kinase) family of lipid kinases regulate cell motility in diverse organisms and cell types. In mammals, the main PI3K enzyme activated by chemokine receptor signalling is the class IB isoform, p110gamma. Studies of p110gamma-knockout mice have shown an essential function for this isoform in chemotaxis of neutrophils and macrophages both in vitro and in vivo. However, the roles of p110gamma and other PI3K enzymes and regulatory subunits in lymphocyte motility have been more difficult to discern. Recent studies of adoptively transferred, fluorescently labelled lymphocytes have revealed complex and unexpected functions for PI3K in lymphocyte migration in vivo. In this review we highlight cell-type-specific roles for PI3K catalytic and regulatory subunits in the homing and basal motility of lymphocytes in the intact lymph node.
脂质激酶的PI3K(磷脂酰肌醇3激酶)家族在多种生物体和细胞类型中调节细胞运动。在哺乳动物中,由趋化因子受体信号激活的主要PI3K酶是IB类亚型p110γ。对p110γ基因敲除小鼠的研究表明,该亚型在体外和体内中性粒细胞和巨噬细胞的趋化作用中具有重要功能。然而,p110γ和其他PI3K酶及调节亚基在淋巴细胞运动中的作用更难辨别。最近对过继转移的荧光标记淋巴细胞的研究揭示了PI3K在体内淋巴细胞迁移中的复杂且意想不到的功能。在本综述中,我们重点介绍了PI3K催化亚基和调节亚基在完整淋巴结中淋巴细胞归巢和基础运动中的细胞类型特异性作用。