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一种用于内吞再循环的含ACAP1的网格蛋白包被复合体。

An ACAP1-containing clathrin coat complex for endocytic recycling.

作者信息

Li Jian, Peters Peter J, Bai Ming, Dai Jun, Bos Erik, Kirchhausen Tomas, Kandror Konstantin V, Hsu Victor W

机构信息

Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, MA 02115, USA.

出版信息

J Cell Biol. 2007 Jul 30;178(3):453-64. doi: 10.1083/jcb.200608033.

DOI:10.1083/jcb.200608033
PMID:17664335
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2064835/
Abstract

Whether coat proteins play a widespread role in endocytic recycling remains unclear. We find that ACAP1, a GTPase-activating protein (GAP) for ADP-ribosylation factor (ARF) 6, is part of a novel clathrin coat complex that is regulated by ARF6 for endocytic recycling in two key physiological settings, stimulation-dependent recycling of integrin that is critical for cell migration and insulin-stimulated recycling of glucose transporter type 4 (Glut4), which is required for glucose homeostasis. These findings not only advance a basic understanding of an early mechanistic step in endocytic recycling but also shed key mechanistic insights into major physiological events for which this transport plays a critical role.

摘要

衣被蛋白是否在胞吞再循环中发挥广泛作用仍不清楚。我们发现,ACAP1是一种针对ADP-核糖基化因子(ARF)6的GTP酶激活蛋白(GAP),它是一种新型网格蛋白衣被复合物的一部分,该复合物在两个关键生理环境中受ARF6调节以进行胞吞再循环,即对细胞迁移至关重要的整合素刺激依赖性再循环,以及葡萄糖稳态所需的胰岛素刺激的4型葡萄糖转运蛋白(Glut4)再循环。这些发现不仅推进了对胞吞再循环早期机制步骤的基本理解,还为这一转运起关键作用的主要生理事件提供了关键的机制见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/121f8e62b275/jcb1780453f08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/ab7c54c60f4b/jcb1780453f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/cc6c4ca75f09/jcb1780453f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/ac6f05402b32/jcb1780453f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/a21d01571233/jcb1780453f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/424239ace5f9/jcb1780453f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/77d38191b60a/jcb1780453f06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/74d4ea40e9cf/jcb1780453f07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/121f8e62b275/jcb1780453f08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/ab7c54c60f4b/jcb1780453f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/cc6c4ca75f09/jcb1780453f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/ac6f05402b32/jcb1780453f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/a21d01571233/jcb1780453f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/424239ace5f9/jcb1780453f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/77d38191b60a/jcb1780453f06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/74d4ea40e9cf/jcb1780453f07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/2064835/121f8e62b275/jcb1780453f08.jpg

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