MircroRNA-145 Attenuates Cardiac Fibrosis Via Regulating Mitogen-Activated Protein Kinase Kinase Kinase 3.


Journal

Cardiovascular drugs and therapy
ISSN: 1573-7241
Titre abrégé: Cardiovasc Drugs Ther
Pays: United States
ID NLM: 8712220

Informations de publication

Date de publication:
08 2023
Historique:
accepted: 29 12 2021
medline: 3 8 2023
pubmed: 14 4 2022
entrez: 13 4 2022
Statut: ppublish

Résumé

This study aimed to explore the effect of microRNA (miR)-145 on cardiac fibrosis in heart failure mice and its target. Experiments were carried out in mice receiving left coronary artery ligation, transverse aortic constriction (TAC), or angiotensin (Ang) II to trigger heart failure, and in cardiac fibroblasts (CFs) with Ang II-induced fibrosis. The miR-145 levels were decreased in the mice hearts of heart failure induced by myocardial infarction (MI), TAC or Ang II infusion, and in the Ang II-treated CFs. The impaired cardiac function was ameliorated by miR-145 agomiR in MI mice. The increased fibrosis and the levels of collagen I, collagen III, and transforming growth factor-beta (TGF-β) in MI mice were inhibited by miR-145 agomiR or miR-145 transgene (TG). The agomiR of miR-145 also attenuated the increases of collagen I, collagen III, and TGF-β in Ang II-treated CFs. Bioinformatics analysis and luciferase reporter assays indicated that mitogen-activated protein kinase kinase kinase 3 (MAP3K3) was a direct target gene of miR-145. MAP3K3 expression was suppressed by MiR-145 in CFs, while the MAP3K3 over-expression reversed the inhibiting effects of miR-145 agomiR on the Ang II-induced increases of collagen I, collagen III, and TGF-β in CFs. These results indicated that miR-145 upregulation could improve cardiac dysfunction and cardiac fibrosis by inhibiting MAP3K3 in heart failure. Thus, upregulating miR-145 or blocking MAP3K3 can be used to treat heart failure and cardiac fibrosis.

Identifiants

pubmed: 35416554
doi: 10.1007/s10557-021-07312-w
pii: 10.1007/s10557-021-07312-w
doi:

Substances chimiques

MicroRNAs 0
MAP Kinase Kinase Kinase 3 EC 2.7.11.25
Collagen 9007-34-5
Transforming Growth Factor beta 0
Angiotensin II 11128-99-7
Transforming Growth Factor beta1 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

655-665

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Yun Liu (Y)

Department of Intensive Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Jing Hu (J)

Research Division of Clinical Pharmacology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Weiwei Wang (W)

Department of Intensive Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Qian Wang (Q)

Pediatric Department, Shanghai General Hospital, No.650 Xinsongjiang Road, Shanghai, 201600, Songjiang District, China. wangq1983@126.com.

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