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Membrane Flow Drives an Adhesion-Independent Amoeboid Cell Migration Mode.膜流驱动非依赖黏附的阿米巴样细胞迁移模式。
Dev Cell. 2018 Jul 2;46(1):9-22.e4. doi: 10.1016/j.devcel.2018.05.029. Epub 2018 Jun 21.
2
Common signalling pathways in macrophage and osteoclast multinucleation.巨噬细胞和破骨细胞多核化的常见信号通路。
J Cell Sci. 2018 Jun 5;131(11):jcs216267. doi: 10.1242/jcs.216267.
3
SRRF: Universal live-cell super-resolution microscopy.SRRF:通用活细胞超分辨率显微镜。
Int J Biochem Cell Biol. 2018 Aug;101:74-79. doi: 10.1016/j.biocel.2018.05.014. Epub 2018 May 28.
4
Membrane Traffic in the Late Steps of Cytokinesis.胞质分裂末期的膜运输。
Curr Biol. 2018 Apr 23;28(8):R458-R470. doi: 10.1016/j.cub.2018.01.019.
5
Optogenetic Control of Cell Migration.细胞迁移的光遗传学控制
Methods Mol Biol. 2018;1749:313-324. doi: 10.1007/978-1-4939-7701-7_22.
6
Semisynthetic fluorescent pH sensors for imaging exocytosis and endocytosis.用于成像胞吐作用和胞吞作用的半合成荧光 pH 传感器。
Nat Commun. 2017 Nov 10;8(1):1412. doi: 10.1038/s41467-017-01752-5.
7
Actomyosin contractility regulators stabilize the cytoplasmic bridge between the two primordial germ cells during embryogenesis.肌动球蛋白收缩调节因子在胚胎发生过程中稳定两个原始生殖细胞之间的细胞质桥。
Mol Biol Cell. 2017 Dec 15;28(26):3789-3800. doi: 10.1091/mbc.E17-08-0502. Epub 2017 Oct 26.
8
Turnover and flow of the cell membrane for cell migration.细胞膜的翻转和流动与细胞迁移。
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9
Nine unanswered questions about cytokinesis.关于胞质分裂的九个未解决问题。
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Real-time imaging of mast cell degranulation in vitro and in vivo.肥大细胞体外和体内脱颗粒的实时成像
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光遗传学控制的 SRRF-Stream 成像显示局部协调的内吞作用和胞吐作用介导的细胞膜重塑。

SRRF-Stream Imaging of Optogenetically Controlled Furrow Formation Shows Localized and Coordinated Endocytosis and Exocytosis Mediating Membrane Remodeling.

出版信息

ACS Synth Biol. 2020 Apr 17;9(4):902-919. doi: 10.1021/acssynbio.9b00521. Epub 2020 Mar 16.

DOI:10.1021/acssynbio.9b00521
PMID:32155337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7194017/
Abstract

Cleavage furrow formation during cytokinesis involves extensive membrane remodeling. In the absence of methods to exert dynamic control over these processes, it has been a challenge to examine the basis of this remodeling. Here we used a subcellular optogenetic approach to induce this at will and found that furrow formation is mediated by actomyosin contractility, retrograde plasma membrane flow, localized decrease in membrane tension, and endocytosis. FRAP, 4-D imaging, and inhibition or upregulation of endocytosis or exocytosis show that ARF6 and Exo70 dependent localized exocytosis supports a potential model for intercellular bridge elongation. TIRF and Super Resolution Radial Fluctuation (SRRF) stream microscopy show localized VAMP2-mediated exocytosis and incorporation of membrane lipids from vesicles into the plasma membrane at the front edge of the nascent daughter cell. Thus, spatially separated but coordinated plasma membrane depletion and addition are likely contributors to membrane remodeling during cytokinetic processes.

摘要

有丝分裂过程中的分裂沟形成涉及广泛的膜重塑。由于缺乏对这些过程进行动态控制的方法,因此研究这种重塑的基础一直是一个挑战。在这里,我们使用亚细胞光遗传学方法来随意诱导这种过程,发现沟的形成是由肌动球蛋白收缩性、逆行质膜流动、局部膜张力降低和胞吞作用介导的。FRAP、4-D 成像以及胞吞作用或胞吐作用的抑制或上调表明,ARF6 和 Exo70 依赖性的局部胞吐作用支持细胞间桥伸长的潜在模型。TIRF 和超分辨率径向波动(SRRF)流显微镜显示,局部 VAMP2 介导的胞吐作用以及从囊泡中将膜脂质掺入到新生子细胞的质膜前缘。因此,在有丝分裂过程中,空间上分离但协调的质膜耗竭和添加可能是膜重塑的贡献因素。