Evidence map›Paper›PMID 25143350›Full record

ArticleAmerican journal of physiology. Cell physiology2014

Pericyte contractility controls endothelial cell cycle progression and sprouting: insights into angiogenic switch mechanics.

Jennifer T Durham, Howard K Surks, Brian M Dulmovits, Ira M Herman

Abstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

36 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  8. MEK1-ERK1/2 signaling regulates the cardiomyocyte non-sarcomeric actin cytoskeletal network.American journal of physiology. Heart and circulatory physiology · 2024
    Article
  9. Review
  10. Biology of vascular mural cells.Development (Cambridge, England) · 2023
    Review
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  12. Article
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  15. Article
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  19. Chemokine-Cytokine Networks in the Head and Neck Tumor Microenvironment.International journal of molecular sciences · 2021
    Review
  20. 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

4 authors at 2 institutions in 1 country.

Jennifer T DurhamGraduate Program in Cellular and Molecular Physiology, Sackler School of Graduate Biomedical Sciences, Department of Developmental, Molecular, and Chemical Biology, Center for Innovations in Wound Healing Research, School of Medicine, Tufts University, Boston, Massachusetts.
Howard K SurksGraduate Program in Cellular and Molecular Physiology, Sackler School of Graduate Biomedical Sciences, Department of Developmental, Molecular, and Chemical Biology, Center for Innovations in Wound Healing Research, School of Medicine, Tufts University, Boston, Massachusetts.
Brian M DulmovitsGraduate Program in Cellular and Molecular Physiology, Sackler School of Graduate Biomedical Sciences, Department of Developmental, Molecular, and Chemical Biology, Center for Innovations in Wound Healing Research, School of Medicine, Tufts University, Boston, Massachusetts.
Ira M HermanGraduate Program in Cellular and Molecular Physiology, Sackler School of Graduate Biomedical Sciences, Department of Developmental, Molecular, and Chemical Biology, Center for Innovations in Wound Healing Research, School of Medicine, Tufts University, Boston, Massachusetts ira.herman@tufts.edu.
Center for Innovation · USTufts University · US

Funding

Training Program in Cardiovascular ResearchT32HL069770 · NHLBI · TUFTS MEDICAL CENTER · PI KARAS, RICHARD H · 2003 to 2013
$4.7M
PATHOBIOLOGY OF DIGESTIVE DISEASEST32DK007542 · NIDDK · TUFTS UNIVERSITY BOSTON · PI LISCUM, LAURA · 1986 to 2010
$3.5M
Adipose Stem Cells for Diabetic RetinopathyR01EY022063 · NEI · UNIVERSITY OF VIRGINIA · PI HERMAN, IRA M, PEIRCE-COTTLER, SHAYN · 2012 to 2015
$2.0M
Regulating retinal microvascular morphogenesisR01EY015125 · NEI · TUFTS UNIVERSITY BOSTON · PI HERMAN, IRA M · 2004 to 2010
$1.7M
Myosin Phosphatase Regulation in Vascular Smooth MuscleR01HL074069 · NHLBI · TUFTS MEDICAL CENTER · PI SURKS, HOWARD K · 2004 to 2008
$1.6M
A new approach to the treatment of Retinopathy of PrematurityK08EY019533 · NEI · UNIVERSITY OF VIRGINIA · PI YATES, PAUL A. · 2009 to 2013
$959k
NEI NIH HHS EY-022063NEI NIH HHS EY-15125NEI NIH HHS EY-19533NEI NIH HHS R01 EY022063NHLBI NIH HHS HL-069770NHLBI NIH HHS HL-074069NIDDK NIH HHS T32 DK-07542
6 · The paper itself

Abstract

Microvascular stability and regulation of capillary tonus are regulated by pericytes and their interactions with endothelial cells (EC). While the RhoA/Rho kinase (ROCK) pathway has been implicated in modulation of pericyte contractility, in part via regulation of the myosin light chain phosphatase (MLCP), the mechanisms linking Rho GTPase activity with actomyosin-based contraction and the cytoskeleton are equivocal. Recently, the myosin phosphatase-RhoA-interacting protein (MRIP) was shown to mediate the RhoA/ROCK-directed MLCP inactivation in vascular smooth muscle. Here we report that MRIP directly interacts with the β-actin-specific capping protein βcap73. Furthermore, manipulation of MRIP expression influences pericyte contractility, with MRIP silencing inducing cytoskeletal remodeling and cellular hypertrophy. MRIP knockdown induces a repositioning of βcap73 from the leading edge to stress fibers; thus MRIP-silenced pericytes increase F-actin-driven cell spreading twofold. These hypertrophied and cytoskeleton-enriched pericytes demonstrate a 2.2-fold increase in contractility upon MRIP knockdown when cells are plated on a deformable substrate. In turn, silencing pericyte MRIP significantly affects EC cycle progression and angiogenic activation. When MRIP-silenced pericytes are cocultured with capillary EC, there is a 2.0-fold increase in EC cycle entry. Furthermore, in three-dimensional models of injury and repair, silencing pericyte MRIP results in a 1.6-fold elevation of total tube area due to EC network formation and increased angiogenic sprouting. The pivotal role of MRIP expression in governing pericyte contractile phenotype and endothelial growth should lend important new insights into how chemomechanical signaling pathways control the "angiogenic switch" and pathological angiogenic induction.

Indexed as

Neovascularization, PhysiologicActin Capping ProteinsAnimalsCattleCell CycleCells, CulturedCell SizeChlorocebus aethiopsCOS CellsCytoskeletonEndothelial CellsEndothelium, VascularHumansMiceMicrofilament ProteinsNIH 3T3 CellsActin Capping ProteinsMicrofilament Proteinsrho-Associated Kinasesangiogenesiscapillarycytoskeletonmural cellmyosin light chainmyosin light chain phosphataseRho kinase

Identifiers

PMID25143350
PMCPMC4216937
OpenAlexW2078959938

What OpenQuestion holds

Textmetadata
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.