Evidence map›Paper›PMID 28536622›Full record

ArticleCellular & molecular biology letters2016

The role of Exo70 in vascular smooth muscle cell migration.

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

Open access · goldAbstract read
In one paragraph

Article in Cellular & molecular biology letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Genome-wide identification of theFrontiers in plant science · 2026
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  5. The Exocyst Complex Subunit EXO70E1-V FromFrontiers in plant science · 2021
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  6. International journal of molecular sciences · 2020
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  10. Identification and Characterization of theInternational journal of molecular sciences · 2018
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  11. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  12. Article
  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Wenqing MaKey Laboratory of Animal Resistant Biology of Shandong, College of Life Science, Shandong Normal University, Jinan, 250014 People's Republic of China.
Yu WangShandong Provincial Hospital affiliated to Shandong University, Jinan, 250014 People's Republic of China.
Xiaomeng YaoKey Laboratory of Animal Resistant Biology of Shandong, College of Life Science, Shandong Normal University, Jinan, 250014 People's Republic of China.
Zijian XuKey Laboratory of Animal Resistant Biology of Shandong, College of Life Science, Shandong Normal University, Jinan, 250014 People's Republic of China.
Liguo AnKey Laboratory of Animal Resistant Biology of Shandong, College of Life Science, Shandong Normal University, Jinan, 250014 People's Republic of China.
Miao YinKey Laboratory of Animal Resistant Biology of Shandong, College of Life Science, Shandong Normal University, Jinan, 250014 People's Republic of China.
Shandong Normal University · CNShandong Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs 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.

methodsImmunofluorescent 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.

resultsThe 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.

conclusionsThis 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.

Indexed as

Cell MovementActinsAnimalsCell LineGene Expression RegulationMuscle, Smooth, VascularRatsTubulinVesicular Transport ProteinsActinsExoc7 protein, ratTubulinVesicular Transport ProteinsCell migrationExo70ExocystImmunohistochemistryRNAiTranswell assayVascular smooth muscle cellWound-healing assay

Identifiers

PMID28536622
PMCPMC5415710
OpenAlexW2536952317

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.