Evidence map›Paper›PMID 32751352›Full record

ArticleInternational journal of molecular sciences2020

RhoA/ROCK Pathway Activation is Regulated by AT1 Receptor and Participates in Smooth Muscle Migration and Dedifferentiation via Promoting Actin Cytoskeleton Polymerization.

Yan Qi, Xiuying Liang, Fan Dai, Haijing Guan, Jingwen Sun, Wenjuan Yao

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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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 1 institution in 1 country.

Yan QiDepartment of Pharmacology, School of Pharmacy, Nantong University, Nantong 226001, Jiangsu, China.
Xiuying LiangDepartment of Pharmacology, School of Pharmacy, Nantong University, Nantong 226001, Jiangsu, China.
Fan DaiDepartment of Pharmacology, School of Pharmacy, Nantong University, Nantong 226001, Jiangsu, China.
Haijing GuanDepartment of Pharmacology, School of Pharmacy, Nantong University, Nantong 226001, Jiangsu, China.
Jingwen SunDepartment of Pharmacology, School of Pharmacy, Nantong University, Nantong 226001, Jiangsu, China.
Wenjuan YaoDepartment of Pharmacology, School of Pharmacy, Nantong University, Nantong 226001, Jiangsu, China.ORCID 0000-0001-7291-1450
Nantong University · CN

Funding

Key University Science Research Project of Jiangsu Province 19KJA320010National Natural Sciences Foundation of China 81970226National Natures Science Foundation of Nantong City JC2018059
6 · The paper itself

Abstract

backgroundIn this study, we investigated the mechanism of Rho GTPases signaling on Ang II-mediated cell migration and dedifferentiation in human aortic vascular smooth muscle cells (HA-VSMCs) and an Ang II-infusion mouse model.

methodsCells were pretreated with different inhibitors or Ang II. Cell migration was detected by Wound healing and Transwell assay. Mice were treated with Ad-RhoA-shRNA virus or Irbesartan or fasudil and then infused with Ang II.

resultsAng II treatment induced HA-VSMCs migration in a dose- and time-dependent manner and reduced the expression of VSMC contractile proteins. These effects were significantly suppressed by the inhibition of Ang II type 1 receptor (AT1 receptor), RhoA, and Rho-associated kinase (ROCK). Furthermore, Ang II treatment promoted the activation of RhoA and ROCK, which was reduced by AT1 receptor inhibition. Meanwhile, Ang II treatment induced F-actin polymerization, which was inhibited after ROCK inhibition. In mice, Ang II infusion increased VSMC migration into the neointima and reduced VSMC differentiation proteins levels, and these effects were shown to be dependent on AT1 receptor and RhoA/ROCK pathway.

conclusionThis study reveals a novel mechanism by which Ang II regulates RhoA/ROCK signaling and actin polymerization via AT1 receptor and then affects VSMC dedifferentiation.

Indexed as

1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineActin CytoskeletonActinsAngiotensin IIAngiotensin II Type 1 Receptor BlockersAnimalsCell DedifferentiationCell LineCell MovementGene Expression RegulationHumansIrbesartanMaleMiceMice, Inbred C57BLMuscle, Smooth, Vascular1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineActinsAngiotensin IIAngiotensin II Type 1 Receptor BlockersfasudilIrbesartanProtein Kinase InhibitorsReceptor, Angiotensin, Type 1rhoA GTP-Binding ProteinRHOA protein, humanrho-Associated KinasesRNA, Small InterferingVasodilator Agentsactinangiotensin IIdedifferentiationmigrationRhoA/ROCK

Identifiers

PMID32751352
PMCPMC7432407
OpenAlexW3045629793

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.