| Literature DB >> 30429362 |
Hiroko Ishiwata-Endo1, Jiro Kato1, Akihiko Tonouchi1, Youn Wook Chung1, Junhui Sun2, Linda A Stevens1, Jianfeng Zhu1, Angel M Aponte3, Danielle A Springer4, Hong San5, Kazuyo Takeda6, Zu-Xi Yu6, Victoria Hoffmann7, Elizabeth Murphy2, Joel Moss1.
Abstract
Mono-ADP-ribosylation of an (arginine) protein catalyzed by ADP-ribosyltransferase 1 (ART1) - i.e., transfer of ADP-ribose from NAD to arginine - is reversed by ADP-ribosylarginine hydrolase 1 (ARH1) cleavage of the ADP-ribose-arginine bond. ARH1-deficient mice developed cardiomyopathy with myocardial fibrosis, decreased myocardial function under dobutamine stress, and increased susceptibility to ischemia/reperfusion injury. The membrane repair protein TRIM72 was identified as a substrate for ART1 and ARH1; ADP-ribosylated TRIM72 levels were greater in ARH1-deficient mice following ischemia/reperfusion injury. To understand better the role of TRIM72 and ADP-ribosylation, we used C2C12 myocytes. ARH1 knockdown in C2C12 myocytes increased ADP-ribosylation of TRIM72 and delayed wound healing in a scratch assay. Mutant TRIM72 (R207K, R260K) that is not ADP-ribosylated interfered with assembly of TRIM72 repair complexes at a site of laser-induced injury. The regulatory enzymes ART1 and ARH1 and their substrate TRIM72 were found in multiple complexes, which were coimmunoprecipitated from mouse heart lysates. In addition, the mono-ADP-ribosylation inhibitors vitamin K1 and novobiocin inhibited oligomerization of TRIM72, the mechanism by which TRIM72 is recruited to the site of injury. We propose that a mono-ADP-ribosylation cycle involving recruitment of TRIM72 and other regulatory factors to sites of membrane damage is critical for membrane repair and wound healing following myocardial injury.Entities:
Keywords: Cardiology; Fibrosis; Heart failure; Mouse models; Muscle Biology
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Year: 2018 PMID: 30429362 PMCID: PMC6302937 DOI: 10.1172/jci.insight.97898
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708