Regulation of Stress Granule Formation by Inflammation, Vascular Injury, and Atherosclerosis.


Journal

Arteriosclerosis, thrombosis, and vascular biology
ISSN: 1524-4636
Titre abrégé: Arterioscler Thromb Vasc Biol
Pays: United States
ID NLM: 9505803

Informations de publication

Date de publication:
10 2019
Historique:
pubmed: 30 8 2019
medline: 19 3 2020
entrez: 30 8 2019
Statut: ppublish

Résumé

Stress granules (SGs) are dynamic cytoplasmic aggregates containing mRNA, RNA-binding proteins, and translation factors that form in response to cellular stress. SGs have been shown to contribute to the pathogenesis of several human diseases, but their role in vascular diseases is unknown. This study shows that SGs accumulate in vascular smooth muscle cells (VSMCs) and macrophages during atherosclerosis. Approach and Results: Immunohistochemical analysis of atherosclerotic plaques from LDLR These results indicate that SG formation is a common feature of the vascular response to injury and disease, and that modification of inflammation reduces stress granule formation in VSMC.

Identifiants

pubmed: 31462091
doi: 10.1161/ATVBAHA.119.313034
pmc: PMC6761003
mid: NIHMS1537613
doi:

Substances chimiques

Poly-ADP-Ribose Binding Proteins 0
RNA Recognition Motif Proteins 0
Cholesterol 97C5T2UQ7J
DNA Helicases EC 3.6.4.-
G3BP1 protein, human EC 3.6.4.12
RNA Helicases EC 3.6.4.13

Types de publication

Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2014-2027

Subventions

Organisme : NHLBI NIH HHS
ID : P01 HL131481
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL141108
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL117724
Pays : United States
Organisme : NHLBI NIH HHS
ID : R35 HL135799
Pays : United States
Organisme : NHLBI NIH HHS
ID : P01 HL131478
Pays : United States

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Auteurs

Allison B Herman (AB)

From the Department of Physiology, Independence Blue Cross Cardiovascular Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.B.H., S.E.K., M.R., C.N.V., R.G.S., M.V.A.).

Milessa Silva Afonso (M)

New York University Langone Health, Leon H. Charney Division of Cardiology, New York (M.S.A., A.C.B., K.M.).

Sheri E Kelemen (SE)

From the Department of Physiology, Independence Blue Cross Cardiovascular Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.B.H., S.E.K., M.R., C.N.V., R.G.S., M.V.A.).

Mitali Ray (M)

From the Department of Physiology, Independence Blue Cross Cardiovascular Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.B.H., S.E.K., M.R., C.N.V., R.G.S., M.V.A.).

Christine N Vrakas (CN)

From the Department of Physiology, Independence Blue Cross Cardiovascular Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.B.H., S.E.K., M.R., C.N.V., R.G.S., M.V.A.).

Amy C Burke (AC)

New York University Langone Health, Leon H. Charney Division of Cardiology, New York (M.S.A., A.C.B., K.M.).

Rosario G Scalia (RG)

From the Department of Physiology, Independence Blue Cross Cardiovascular Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.B.H., S.E.K., M.R., C.N.V., R.G.S., M.V.A.).

Kathryn Moore (K)

New York University Langone Health, Leon H. Charney Division of Cardiology, New York (M.S.A., A.C.B., K.M.).

Michael V Autieri (MV)

From the Department of Physiology, Independence Blue Cross Cardiovascular Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.B.H., S.E.K., M.R., C.N.V., R.G.S., M.V.A.).

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Classifications MeSH