Active RhoA Exerts an Inhibitory Effect on the Homeostasis and Angiogenic Capacity of Human Endothelial Cells.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
21 06 2022
Historique:
pubmed: 15 6 2022
medline: 24 6 2022
entrez: 14 6 2022
Statut: ppublish

Résumé

Background The small GTPase RhoA (Ras homolog gene family, member A) regulates a variety of cellular processes, including cell motility, proliferation, survival, and permeability. In addition, there are reports indicating that RhoA-ROCK (rho associated coiled-coil containing protein kinase) activation is essential for VEGF (vascular endothelial growth factor)-mediated angiogenesis, whereas other work suggests VEGF-antagonistic effects of the RhoA-ROCK axis. Methods and Results To elucidate this issue, we examined human umbilical vein endothelial cells and human coronary artery endothelial cells after stable overexpression (lentiviral transduction) of constitutively active (G14V/Q63L), dominant-negative (T19N), or wild-type RhoA using a series of in vitro angiogenesis assays (proliferation, migration, tube formation, angiogenic sprouting, endothelial cell viability) and a human umbilical vein endothelial cells xenograft assay in immune-incompetent NOD

Identifiants

pubmed: 35699166
doi: 10.1161/JAHA.121.025119
pmc: PMC9238636
doi:

Substances chimiques

Vascular Endothelial Growth Factor A 0
RHOA protein, human 124671-05-2
LIMK1 protein, human EC 2.7.11.1
Lim Kinases EC 2.7.11.1
ROCK1 protein, human EC 2.7.11.1
rho-Associated Kinases EC 2.7.11.1
rhoA GTP-Binding Protein EC 3.6.5.2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e025119

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Auteurs

Michael Hauke (M)

Department of Clinical Pharmacy and Pharmacotherapy Institute of PharmacyMartin-Luther-University Halle-Wittenberg Halle (Saale) Germany.

Robert Eckenstaler (R)

Department of Clinical Pharmacy and Pharmacotherapy Institute of PharmacyMartin-Luther-University Halle-Wittenberg Halle (Saale) Germany.

Anne Ripperger (A)

Department of Clinical Pharmacy and Pharmacotherapy Institute of PharmacyMartin-Luther-University Halle-Wittenberg Halle (Saale) Germany.

Anna Ender (A)

Department of Clinical Pharmacy and Pharmacotherapy Institute of PharmacyMartin-Luther-University Halle-Wittenberg Halle (Saale) Germany.

Heike Braun (H)

Department of Clinical Pharmacy and Pharmacotherapy Institute of PharmacyMartin-Luther-University Halle-Wittenberg Halle (Saale) Germany.

Ralf A Benndorf (RA)

Department of Clinical Pharmacy and Pharmacotherapy Institute of PharmacyMartin-Luther-University Halle-Wittenberg Halle (Saale) Germany.

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Classifications MeSH