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Rac1和RhoA的协同平衡在决定吞噬能力方面起着关键作用。

Coordinated balance of Rac1 and RhoA plays key roles in determining phagocytic appetite.

作者信息

Kim Sang-Yeob, Kim Soyoun, Bae Dong-Jun, Park Seung-Yoon, Lee Ga-Young, Park Gyeong-Min, Kim In-San

机构信息

Department of Biochemistry and Cell Biology, Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.

ASAN Institute for Life Sciences, ASAN Medical Center, Seoul, Republic of Korea.

出版信息

PLoS One. 2017 Apr 4;12(4):e0174603. doi: 10.1371/journal.pone.0174603. eCollection 2017.

DOI:10.1371/journal.pone.0174603
PMID:28376111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5380344/
Abstract

The removal of unwanted or damaged cells by phagocytes is achieved via a finely regulated cleaning process called efferocytosis. To characterize the mechanisms through which phagocytes control the intake of apoptotic cells, we investigated how the phagocyte's appetite for engulfed cells may be coordinated by RhoA and Rac1 in the phagocytic cup. We used FRET biosensors to visualize the spatiotemporal dynamics of Rho-family GTPases, and found that RhoA, which is known to be downregulated during phagocytosis, was transiently upregulated at the phagocytic cup immediately prior to ingestion. Conversely, Rac1 was upregulated during the engulfment process and then downregulated prior to phagosomal maturation. Moreover, disturbance of the dynamic activities of RhoA led to uncontrolled engulfment, such as fast and undiscerning eating. Our results reveal that the temporal activity of RhoA GTPase alters the Rac1/RhoA balance at the phagocytic cup prior to ingestion, and that this plays a distinct role in orchestrating efferocytosis, with RhoA modulating the rate of engulfment to ensure that the phagocyte engulfs an appropriate amount of the correct material.

摘要

吞噬细胞通过一种称为胞葬作用的精细调控的清除过程来清除不需要的或受损的细胞。为了阐明吞噬细胞控制凋亡细胞摄取的机制,我们研究了吞噬杯中的RhoA和Rac1如何协调吞噬细胞对被吞噬细胞的吞噬能力。我们使用荧光共振能量转移(FRET)生物传感器来观察Rho家族小GTP酶的时空动态变化,发现已知在吞噬过程中表达下调的RhoA在吞噬前瞬间在吞噬杯处短暂上调。相反,Rac1在吞噬过程中上调,然后在吞噬体成熟前下调。此外,RhoA动态活性的紊乱导致吞噬失控,如快速且不加区分的吞噬。我们的结果表明,RhoA GTP酶的瞬时活性在吞噬前改变了吞噬杯处的Rac1/RhoA平衡,这在协调胞葬作用中起着独特的作用,RhoA调节吞噬速率以确保吞噬细胞吞噬适量的正确物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/01d3ad189ab1/pone.0174603.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/af877d96b416/pone.0174603.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/04620586b66c/pone.0174603.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/4c01173b4b05/pone.0174603.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/319327d24ee0/pone.0174603.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/01d3ad189ab1/pone.0174603.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/af877d96b416/pone.0174603.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/04620586b66c/pone.0174603.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/4c01173b4b05/pone.0174603.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/319327d24ee0/pone.0174603.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b9/5380344/01d3ad189ab1/pone.0174603.g005.jpg

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