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在运动细胞前缘的背侧和腹侧表面以及静止细胞的突起上,包被小窝的不对称形成。

Asymmetric formation of coated pits on dorsal and ventral surfaces at the leading edges of motile cells and on protrusions of immobile cells.

作者信息

Kural Comert, Akatay Ahmet Ata, Gaudin Raphaël, Chen Bi-Chang, Legant Wesley R, Betzig Eric, Kirchhausen Tom

机构信息

Department of Cell Biology, Harvard Medical School, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115 Department of Physics, The Ohio State University, Columbus, OH 43210

Biophysics Graduate Program, The Ohio State University, Columbus, OH 43210.

出版信息

Mol Biol Cell. 2015 Jun 1;26(11):2044-53. doi: 10.1091/mbc.E15-01-0055. Epub 2015 Apr 7.

DOI:10.1091/mbc.E15-01-0055
PMID:25851602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4472015/
Abstract

Clathrin/AP2-coated vesicles are the principal endocytic carriers originating at the plasma membrane. In the experiments reported here, we used spinning-disk confocal and lattice light-sheet microscopy to study the assembly dynamics of coated pits on the dorsal and ventral membranes of migrating U373 glioblastoma cells stably expressing AP2 tagged with enhanced green fluorescence (AP2-EGFP) and on lateral protrusions from immobile SUM159 breast carcinoma cells, gene-edited to express AP2-EGFP. On U373 cells, coated pits initiated on the dorsal membrane at the front of the lamellipodium and at the approximate boundary between the lamellipodium and lamella and continued to grow as they were swept back toward the cell body; coated pits were absent from the corresponding ventral membrane. We observed a similar dorsal/ventral asymmetry on membrane protrusions from SUM159 cells. Stationary coated pits formed and budded on the remainder of the dorsal and ventral surfaces of both types of cells. These observations support a previously proposed model that invokes net membrane deposition at the leading edge due to an imbalance between the endocytic and exocytic membrane flow at the front of a migrating cell.

摘要

网格蛋白/AP2包被囊泡是源自质膜的主要内吞载体。在本文报道的实验中,我们使用转盘共聚焦显微镜和晶格层光显微镜,研究了稳定表达增强型绿色荧光标记的AP2(AP2-EGFP)的迁移U373胶质母细胞瘤细胞背膜和腹膜上包被小窝的组装动力学,以及经基因编辑以表达AP2-EGFP的静止SUM159乳腺癌细胞的侧向突起上包被小窝的组装动力学。在U373细胞上,包被小窝在片状伪足前端的背膜以及片状伪足与片层之间的大致边界处起始,并在它们被扫向细胞体时继续生长;相应的腹膜上没有包被小窝。我们在SUM159细胞的膜突起上观察到了类似的背/腹不对称性。在这两种细胞的背表面和腹表面的其余部分形成并出芽了静止的包被小窝。这些观察结果支持了先前提出的一个模型,该模型认为由于迁移细胞前端内吞和外吐膜流之间的不平衡,导致在前缘有净膜沉积。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/b0ec7bd37b00/2044fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/8ea45c3e4cd6/2044fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/1665ce3dc880/2044fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/110cc992b718/2044fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/a2c8c7c550cd/2044fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/8645c6514fea/2044fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/b0ec7bd37b00/2044fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/8ea45c3e4cd6/2044fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/1665ce3dc880/2044fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/110cc992b718/2044fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/a2c8c7c550cd/2044fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/8645c6514fea/2044fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/339a/4472015/b0ec7bd37b00/2044fig6.jpg

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