Annexin A4 N-terminal peptide inhibits adenylyl cyclase 5 and limits β-adrenoceptor-mediated prolongation of cardiac action potential.


Journal

FASEB journal : official publication of the Federation of American Societies for Experimental Biology
ISSN: 1530-6860
Titre abrégé: FASEB J
Pays: United States
ID NLM: 8804484

Informations de publication

Date de publication:
08 2020
Historique:
received: 19 08 2019
revised: 08 05 2020
accepted: 26 05 2020
pubmed: 25 6 2020
medline: 2 3 2021
entrez: 25 6 2020
Statut: ppublish

Résumé

Adenylyl cyclases (AC) are essential for the normal and pathophysiological response of many cells. In cardiomyocytes, the predominant AC isoforms are AC5 and AC6. Specific AC5 inhibition was suggested as an option for the treatment of heart failure potentially advantageous over β-blockers. We previously reported an interaction between the calcium-binding protein annexin A4 (ANXA4) and AC5 in human embryonic kidney 293 (HEK293) cells and an inhibition of cyclic adenosine monophosphate (cAMP) production in cardiomyocytes. Here, we investigated whether ANXA4 is able to differentiate between AC5 and AC6. In transfected HEK293 cells, ANXA4 specifically co-immunoprecipitated with AC5 and not with AC6, via its N-terminal domain. Both ANXA4 and a peptide comprising the ANXA4 N-terminal sequence (A4N

Identifiants

pubmed: 32579290
doi: 10.1096/fj.201902094RR
doi:

Substances chimiques

Annexin A4 0
Calcium Channels, L-Type 0
Receptors, Adrenergic 0
Cyclic AMP E0399OZS9N
Adenylyl Cyclases EC 4.6.1.1

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

10489-10504

Informations de copyright

© 2020 The Authors. The FASEB Journal published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology.

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Auteurs

Alexander Heinick (A)

Institute of Pharmacology and Toxicology, University of Münster, Münster, Germany.

Florentina Pluteanu (F)

Institute of Pharmacology and Toxicology, University of Münster, Münster, Germany.

Christina Hermes (C)

Institute of Pharmacology and Toxicology, University of Münster, Münster, Germany.

Andre Klemme (A)

Institute of Pharmacology and Toxicology, University of Münster, Münster, Germany.

Manuel Domnik (M)

Institute of Pharmacology and Toxicology, University of Münster, Münster, Germany.

Xenia Husser (X)

Institute of Pharmacology and Toxicology, University of Münster, Münster, Germany.

Volker Gerke (V)

Institute of Medical Biochemistry, Center for Molecular Biology of Inflammation, University of Münster, Münster, Germany.
Interdisciplinary Clinical Research Center, University of Münster, Münster, Germany.

Wilhelm Schmitz (W)

Institute of Pharmacology and Toxicology, University of Münster, Münster, Germany.

Frank U Müller (FU)

Institute of Pharmacology and Toxicology, University of Münster, Münster, Germany.

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