Evidence map›Paper›PMID 22287273›Full record

ArticleJournal of cellular physiology2012

Src modulates contractile vascular smooth muscle function via regulation of focal adhesions.

Jianghong Min, Maya Reznichenko, Ransom H Poythress, Cynthia M Gallant, Susanne Vetterkind, Yunping Li, Kathleen G Morgan

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  9. Molecular therapy. Nucleic acids · 2020
    Article
  10. EPAC in Vascular Smooth Muscle Cells.International journal of molecular sciences · 2020
    Review
  11. Article
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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

7 authors at 2 institutions in 1 country.

Jianghong MinDepartment of Health Sciences, Boston University, Boston, MA 02215, USA.
Maya Reznichenko
Ransom H Poythress
Cynthia M Gallant
Susanne Vetterkind
Yunping Li
Kathleen G Morgan
Boston University · USHarvard University · US

Funding

Structure-Function of the CytoskeletonP01HL086655 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MORGAN, KATHLEEN G · 2007 to 2011
$8.8M
REGULATION OF CONTRACTION OF BLOOD VESSELSR01HL031704 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MORGAN, KATHLEEN G · 1985 to 2009
$3.7M
Subcellular Organization of Signaling in Smooth MuscleR01HL080003 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MORGAN, KATHLEEN G · 2006 to 2009
$1.7M
NHLBI NIH HHS HL080003NHLBI NIH HHS HL086655NHLBI NIH HHS HL31704NHLBI NIH HHS P01 HL086655NHLBI NIH HHS R01 HL031704NHLBI NIH HHS R01 HL080003
6 · The paper itself

Abstract

Src is a known regulator of focal adhesion turnover in migrating cells; but, in contrast, Src is generally assumed to play little role in differentiated, contractile vascular smooth muscle (dVSM). The goal of the present study was to determine if Src-family kinases regulate focal adhesion proteins and how this might affect contractility of non-proliferative vascular smooth muscle. We demonstrate here, through the use of phosphotyrosine screening, deconvolution microscopy imaging, and differential centrifugation, that the activity of Src family kinases in aorta is regulated by the alpha agonist and vasoconstrictor phenylephrine, and leads to focal adhesion protein phosphorylation and remodeling in dVSM. Furthermore, Src inhibition via morpholino knockdown of Src or by the small molecule inhibitor PP2 prevents phenylephrine-induced adhesion protein phosphorylation, markedly slows the tissue's ability to contract, and decreases steady state contractile force amplitude. Significant vasoconstrictor-induced and Src-dependent phosphorylation of Cas pY-165, FAK pY-925, paxillin pY-118, and Erk1/2 were observed. However, increases in FAK 397 phosphorylation were not seen, demonstrating differences between cells in tissue versus migrating, proliferating cells. We show here that Src, in a cause and effect manner, regulates focal adhesion protein function and, consequently, modulates contractility during the action of a vasoconstrictor. These data point to the possibility that vascular focal adhesion proteins may be useful drug discovery targets for novel therapeutic approaches to cardiovascular disease.

Indexed as

src-Family KinasesAnimalsAortaFerretsFocal Adhesion Protein-Tyrosine KinasesFocal AdhesionsGene Knockdown TechniquesHumansMuscle ContractionMuscle, Smooth, VascularOrgan Culture TechniquesPhenylephrinePhosphorylationPhosphotyrosinePyrimidinesSignal TransductionAG 1879Focal Adhesion Protein-Tyrosine KinasesPhenylephrinePhosphotyrosinePyrimidinessrc-Family Kinases

Identifiers

PMID22287273
PMCPMC3348426
OpenAlexW1982488622

What OpenQuestion holds

Textmetadata
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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.