Lam Trang T, Chong Mark M W
St Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.
Department of Medicine (St Vincent's), University of Melbourne, Fitzroy, VIC, Australia.
Front Immunol. 2025 Jun 10;16:1622928. doi: 10.3389/fimmu.2025.1622928. eCollection 2025.
T cell development and function depend on precise remodeling of the actin cytoskeleton, which regulates migration, cell division, immunological synapse formation, and signal transduction. Regulators of actin include nucleators (Arp2/3, Formins) and binding proteins (coronins, cofilin, myosin) that orchestrate cytoskeletal dynamics to ensure efficient antigen recognition and signaling, while Rho GTPases (Rac1, Cdc42, RhoA) link extracellular cues to actin rearrangements, influencing both conventional T cell activation and function. Dysregulated actin dynamics contribute to immunodeficiencies and autoimmunity, and thus understanding how the actin cytoskeleton is regulated in T cells has important implications.
T细胞的发育和功能依赖于肌动蛋白细胞骨架的精确重塑,该骨架调节迁移、细胞分裂、免疫突触形成和信号转导。肌动蛋白的调节因子包括成核因子(Arp2/3、Formins)和结合蛋白(冠蛋白、丝切蛋白、肌球蛋白),它们协调细胞骨架动力学以确保有效的抗原识别和信号传导,而Rho GTP酶(Rac1、Cdc42、RhoA)将细胞外信号与肌动蛋白重排联系起来,影响传统T细胞的激活和功能。肌动蛋白动力学失调会导致免疫缺陷和自身免疫,因此了解T细胞中肌动蛋白细胞骨架是如何被调节具有重要意义。