The State Key Laboratory of Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Immunology. 2012 Apr;135(4):268-75. doi: 10.1111/j.1365-2567.2011.03549.x.
Integrins not only mediate cell-cell and cell-extracellular matrix adhesion, but also affect the multitude of signal transduction cascades in control of cell survival, proliferation, differentiation and organ development. Mutations in integrins or the major effectors of integrin signalling pathways cause defective organ development, immunodeficiency, cancer or autoimmune disease. Understanding of the signalling events that drive integrin activation and signalling is therefore crucial to uncover the molecular mechanisms of these diseases. This review discusses the key signalling complexes regulating integrin activation and function in both 'inside-out' and 'outside-in' pathways in T lymphocytes, including kinases, SLP-76, VAV1, ADAP, SKAP-55, RapL, RIAM, Rap1, Talin and Kindlin.
整合素不仅介导细胞-细胞和细胞-细胞外基质的黏附,还影响多种信号转导级联反应,从而控制细胞的存活、增殖、分化和器官发育。整合素或整合素信号通路的主要效应因子的突变会导致器官发育缺陷、免疫缺陷、癌症或自身免疫性疾病。因此,了解驱动整合素激活和信号转导的信号事件对于揭示这些疾病的分子机制至关重要。本综述讨论了调节 T 淋巴细胞中“内-外”和“外-内”途径的整合素激活和功能的关键信号复合物,包括激酶、SLP-76、VAV1、ADAP、SKAP-55、RapL、RIAM、Rap1、Talin 和 Kindlin。