Long Non-coding RNA Aerrie Controls DNA Damage Repair via YBX1 to Maintain Endothelial Cell Function.

DNA damage LncRNA – long non-coding RNA aging cardiovascular disease endothelial cell

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2020
Historique:
received: 19 10 2020
accepted: 07 12 2020
entrez: 28 1 2021
pubmed: 29 1 2021
medline: 29 1 2021
Statut: epublish

Résumé

Aging is accompanied by many physiological changes. These changes can progressively lead to many types of cardiovascular diseases. During this process blood vessels lose their ability to maintain vascular homeostasis, ultimately resulting in hypertension, stroke, or myocardial infarction. Increase in DNA damage is one of the hallmarks of aging and can be repaired by the DNA signaling and repair system. In our study we show that long non-coding RNA Aerrie (linc01013) contributes to the DNA signaling and repair mechanism. Silencing of Aerrie in endothelial cells impairs angiogenesis, migration, and barrier function. Aerrie associates with YBX1 and together they act as important factors in DNA damage signaling and repair. This study identifies Aerrie as a novel factor in genomic stability and as a binding partner of YBX1 in responding to DNA damage.

Identifiants

pubmed: 33505972
doi: 10.3389/fcell.2020.619079
pmc: PMC7829583
doi:

Types de publication

Journal Article

Langues

eng

Pagination

619079

Informations de copyright

Copyright © 2021 Pham, Bink, Stanicek, van Bergen, van Leeuwen, Tran, Matic, Hedin, Wittig, Dimmeler and Boon.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Tan Phát Pham (TP)

Department of Physiology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Diewertje I Bink (DI)

Department of Physiology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Laura Stanicek (L)

Department of Physiology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Institute of Cardiovascular Regeneration, Goethe University, Frankfurt, Germany.

Anke van Bergen (A)

Department of Physiology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Esmee van Leeuwen (E)

Department of Physiology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Yvonne Tran (Y)

Department of Physiology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Ljubica Matic (L)

Vascular Surgery Division, Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

Ulf Hedin (U)

Vascular Surgery Division, Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

Ilka Wittig (I)

Institute of Cardiovascular Regeneration, Goethe University, Frankfurt, Germany.

Stefanie Dimmeler (S)

Institute of Cardiovascular Regeneration, Goethe University, Frankfurt, Germany.
German Center for Cardiovascular Research DZHK, Partner Site Frankfurt Rhine-Main, Berlin, Germany.

Reinier A Boon (RA)

Department of Physiology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Institute of Cardiovascular Regeneration, Goethe University, Frankfurt, Germany.
German Center for Cardiovascular Research DZHK, Partner Site Frankfurt Rhine-Main, Berlin, Germany.

Classifications MeSH