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本文引用的文献

1
T Lymphocyte Myosin IIA is Required for Maturation of the Immunological Synapse.T 淋巴细胞肌球蛋白 IIA 对于免疫突触的成熟是必需的。
Front Immunol. 2012 Aug 17;3:230. doi: 10.3389/fimmu.2012.00230. eCollection 2012.
2
Integration of the movement of signaling microclusters with cellular motility in immunological synapses.信号微簇的运动与免疫突触中细胞运动的整合。
Nat Immunol. 2012 Jul 1;13(8):787-95. doi: 10.1038/ni.2364.
3
F-actin polymerization and retrograde flow drive sustained PLCγ1 signaling during T cell activation.F-actin 聚合和逆行流驱动 T 细胞激活过程中 PLCγ1 的持续信号转导。
J Cell Biol. 2012 Jun 11;197(6):775-87. doi: 10.1083/jcb.201201018. Epub 2012 Jun 4.
4
Actin stress fibers--assembly, dynamics and biological roles.肌动蛋白应力纤维——组装、动力学和生物学功能。
J Cell Sci. 2012 Apr 15;125(Pt 8):1855-64. doi: 10.1242/jcs.098087. Epub 2012 Apr 29.
5
Receptor signaling clusters in the immune synapse.免疫突触中的受体信号簇。
Annu Rev Biophys. 2012;41:543-56. doi: 10.1146/annurev-biophys-042910-155238. Epub 2012 Feb 23.
6
Myosin IIA modulates T cell receptor transport and CasL phosphorylation during early immunological synapse formation.肌球蛋白 IIA 在早期免疫突触形成过程中调节 T 细胞受体运输和 CasL 磷酸化。
PLoS One. 2012;7(2):e30704. doi: 10.1371/journal.pone.0030704. Epub 2012 Feb 8.
7
Mechanosensing in T lymphocyte activation.T 淋巴细胞激活中的机械感知。
Biophys J. 2012 Jan 18;102(2):L5-7. doi: 10.1016/j.bpj.2011.12.011.
8
Actin retrograde flow and actomyosin II arc contraction drive receptor cluster dynamics at the immunological synapse in Jurkat T cells.肌动蛋白逆行流动和肌球蛋白 II 弧形收缩驱动 Jurkat T 细胞免疫突触中受体簇的动力学。
Mol Biol Cell. 2012 Mar;23(5):834-52. doi: 10.1091/mbc.E11-08-0731. Epub 2012 Jan 4.
9
Formins filter modified actin subunits during processive elongation.成核因子在延伸过程中过滤修饰的肌动蛋白亚基。
J Struct Biol. 2012 Jan;177(1):32-9. doi: 10.1016/j.jsb.2011.10.005. Epub 2011 Oct 25.
10
Remodelling of cortical actin where lytic granules dock at natural killer cell immune synapses revealed by super-resolution microscopy.通过超分辨率显微镜揭示了溶酶体颗粒在自然杀伤细胞免疫突触处停靠时皮质肌动蛋白的重塑。
PLoS Biol. 2011 Sep;9(9):e1001152. doi: 10.1371/journal.pbio.1001152. Epub 2011 Sep 13.

肌球蛋白 II 在免疫突触中的功能存在争议和共识。

Controversy and consensus regarding myosin II function at the immunological synapse.

机构信息

Cell Biology and Physiology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892-8017, USA.

出版信息

Curr Opin Immunol. 2013 Jun;25(3):300-6. doi: 10.1016/j.coi.2013.03.010. Epub 2013 Apr 24.

DOI:10.1016/j.coi.2013.03.010
PMID:23623641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3691351/
Abstract

Regulated actin dynamics play a central role in modulating signaling events at the immunological synapse (IS). Polymerization of actin filaments at the periphery of the IS, coupled to depolymerization near the center, generates a centripetal flow of the actin network and associated movement of signaling molecules. A recent flurry of papers addresses the role of myosin II in facilitating these events. Investigators agree that myosin II is present at the IS, where it forms actomyosin arcs within the peripheral supramolecular activation cluster, a region corresponding to the lamellum of migrating cells. However, there is substantial disagreement about the extent to which myosin II drives IS formation and signaling events leading to T cell activation.

摘要

规管肌动蛋白动力学在调节免疫突触 (IS) 中的信号事件中起着核心作用。IS 周边的肌动蛋白丝聚合,与中心附近的解聚相结合,产生肌动蛋白网络向心流动和相关信号分子的运动。最近有大量论文探讨了肌球蛋白 II 在促进这些事件中的作用。研究人员一致认为,肌球蛋白 II 存在于 IS 中,在那里它在周边超分子激活簇内形成肌球蛋白-肌动蛋白弧,这一区域对应于迁移细胞的片层。然而,对于肌球蛋白 II 在多大程度上驱动 IS 的形成以及导致 T 细胞激活的信号事件,存在着很大的分歧。