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Exo70在血管平滑肌细胞迁移中的作用。

The role of Exo70 in vascular smooth muscle cell migration.

作者信息

Ma Wenqing, Wang Yu, Yao Xiaomeng, Xu Zijian, An Liguo, Yin Miao

机构信息

Key Laboratory of Animal Resistant Biology of Shandong, College of Life Science, Shandong Normal University, Jinan, 250014 People's Republic of China.

Shandong Provincial Hospital affiliated to Shandong University, Jinan, 250014 People's Republic of China.

出版信息

Cell Mol Biol Lett. 2016 Sep 22;21:20. doi: 10.1186/s11658-016-0019-8. eCollection 2016.

Abstract

BACKGROUND

As a key subunit of the exocyst complex, Exo70 has highly conserved sequence and is widely found in yeast, mammals, and plants. In yeast, Exo70 mediates the process of exocytosis and promotes anchoring and integration of vesicles with the plasma membrane. In mammalian cells, Exo70 is involved in maintaining cell morphology, cell migration, cell connection, mRNA splicing, and other physiological processes, as well as participating in exocytosis. However, Exo70's function in mammalian cells has yet to be fully recognized. In this paper, the expression of Exo70 and its role in cell migration were studied in a rat vascular smooth muscle cell line A7r5.

METHODS

Immunofluorescent analysis the expression of Exo70, α-actin, and tubulin in A7r5 cells showed a co-localization of Exo70 and α-actin, we treated the cells with cytochalasin B to depolymerize α-actin, in order to further confirm the co-localization of Exo70 and α-actin. We analyzed Exo70 co-localization with actin at the edge of migrating cells by wound-healing assay to establish whether Exo70 might play a role in cell migration. Next, we analyzed the migration and invasion ability of A7r5 cells before and after RNAi silencing through the wound healing assay and transwell assay.

RESULTS

The mechanism of interaction between Exo70 and cytoskeleton can be clarified by the immunoprecipitation techniques and wound-healing assay. The results showed that Exo70 and α-actin were co-localized at the leading edge of migrating cells. The ability of A7r5 to undergo cell migration was decreased when Exo70 expression was silenced by RNAi. Reducing Exo70 expression in RNAi treated A7r5 cells significantly lowered the invasion and migration ability of these cells compared to the normal cells. These results indicate that Exo70 participates in the process of A7r5 cell migration.

CONCLUSIONS

This research is importance for the study on the pathological process of vascular intimal hyperplasia, since it provides a new research direction for the treatment of cardiovascular diseases such as atherosclerosis and restenosis after balloon angioplasty.

摘要

背景

作为外泌体复合体的关键亚基,Exo70具有高度保守的序列,广泛存在于酵母、哺乳动物和植物中。在酵母中,Exo70介导胞吐过程,促进囊泡与质膜的锚定和融合。在哺乳动物细胞中,Exo70参与维持细胞形态、细胞迁移、细胞连接、mRNA剪接等生理过程,以及参与胞吐作用。然而,Exo70在哺乳动物细胞中的功能尚未得到充分认识。本文在大鼠血管平滑肌细胞系A7r5中研究了Exo70的表达及其在细胞迁移中的作用。

方法

免疫荧光分析A7r5细胞中Exo70、α-肌动蛋白和微管蛋白的表达,结果显示Exo70与α-肌动蛋白共定位,我们用细胞松弛素B处理细胞使α-肌动蛋白解聚,以进一步证实Exo70与α-肌动蛋白的共定位。我们通过划痕实验分析迁移细胞边缘处Exo70与肌动蛋白的共定位,以确定Exo70是否可能在细胞迁移中发挥作用。接下来,我们通过划痕实验和Transwell实验分析RNA干扰沉默前后A7r5细胞的迁移和侵袭能力。

结果

免疫沉淀技术和划痕实验可阐明Exo70与细胞骨架之间的相互作用机制。结果显示,Exo70与α-肌动蛋白在迁移细胞的前沿共定位。当通过RNA干扰使Exo70表达沉默时,A7r5细胞的迁移能力下降。与正常细胞相比,RNA干扰处理的A7r5细胞中Exo70表达的降低显著降低了这些细胞的侵袭和迁移能力。这些结果表明,Exo70参与A7r5细胞迁移过程。

结论

本研究对血管内膜增生病理过程的研究具有重要意义,为动脉粥样硬化和球囊血管成形术后再狭窄等心血管疾病的治疗提供了新的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48ff/5415710/4525ba13c416/11658_2016_19_Fig1_HTML.jpg

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