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对出芽酵母酿酒酵母中内体和肌动蛋白斑的组装、拆卸以及肌动蛋白丝束依赖性运动进行活细胞成像。

Live cell imaging of the assembly, disassembly, and actin cable-dependent movement of endosomes and actin patches in the budding yeast, Saccharomyces cerevisiae.

作者信息

Huckaba Thomas M, Gay Anna Card, Pantalena Luiz Fernando, Yang Hyeong-Cheol, Pon Liza A

机构信息

Department of Anatomy and Cell Biology, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.

出版信息

J Cell Biol. 2004 Nov 8;167(3):519-30. doi: 10.1083/jcb.200404173.

Abstract

Using FM4-64 to label endosomes and Abp1p-GFP or Sac6p-GFP to label actin patches, we find that (1) endosomes colocalize with actin patches as they assemble at the bud cortex; (2) endosomes colocalize with actin patches as they undergo linear, retrograde movement from buds toward mother cells; and (3) actin patches interact with and disassemble at FM4-64-labeled internal compartments. We also show that retrograde flow of actin cables mediates retrograde actin patch movement. An Arp2/3 complex mutation decreases the frequency of cortical, nonlinear actin patch movements, but has no effect on the velocity of linear, retrograde actin patch movement. Rather, linear actin patch movement occurs at the same velocity and direction as the movement of actin cables. Moreover, actin patches require actin cables for retrograde movements and colocalize with actin cables as they undergo retrograde movement. Our studies support a mechanism whereby actin cables serve as "conveyor belts" for retrograde movement and delivery of actin patches/endosomes to FM4-64-labeled internal compartments.

摘要

使用FM4-64标记内体,并用Abp1p-GFP或Sac6p-GFP标记肌动蛋白斑,我们发现:(1)内体在芽皮层组装时与肌动蛋白斑共定位;(2)内体在从芽向母细胞进行线性逆行移动时与肌动蛋白斑共定位;(3)肌动蛋白斑与FM4-64标记的内部区室相互作用并在其处解体。我们还表明,肌动蛋白电缆的逆行流动介导了肌动蛋白斑的逆行移动。Arp2/3复合体突变降低了皮层非线性肌动蛋白斑移动的频率,但对线性逆行肌动蛋白斑移动的速度没有影响。相反,线性肌动蛋白斑移动的速度和方向与肌动蛋白电缆的移动相同。此外,肌动蛋白斑逆行移动需要肌动蛋白电缆,并在逆行移动时与肌动蛋白电缆共定位。我们的研究支持一种机制,即肌动蛋白电缆充当“传送带”,用于肌动蛋白斑/内体的逆行移动以及将其递送至FM4-64标记的内部区室。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b42a/2172478/ebe1a1d5e56f/200404173f1.jpg

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