| Literature DB >> 29409895 |
Yui Inomata1, Shouta Nagasaka1, Kazuki Miyate1, Yuta Goto1, Chizuru Hino1, Chihiro Toukairin1, Rieko Higashio1, Kinji Ishida2, Tomoyuki Saino3, Masamichi Hirose4, Hideki Tsumura5, Atsushi Sanbe6.
Abstract
Bcl-2-associated athanogene 3 (BAG3) is strongly expressed in both cardiac and skeletal muscle. A recent study showed that BAG3 may play a protective role in muscles. Little is known, however, regarding the detailed role of BAG3 in cardiac muscle. To better understand the functional role of cardiac BAG3 in the heart, we generated transgenic (TG) mice that overexpress BAG3. A decrease in fractional shortening, and the induction of cardiac atrial natriuretic peptide, were observed in BAG3 TG mice. Moreover, a marked reduction in the protein level of small HSPs was detected in BAG3 TG mouse hearts. We analyzed the cardiac small HSP levels when either the ubiquitin-proteasome system (UPS) or the autophagy system (AS) was inhibited in BAG3 TG mice. The protein turnovers of small HSPs by the AS were activated in BAG3 TG mouse hearts. Thus, BAG3 is critical for the protein turnover of small HSPs via activation of autophagy in the heart.Entities:
Keywords: Cardiac function; Heat shock protein; Transgenic mouse
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Year: 2018 PMID: 29409895 DOI: 10.1016/j.bbrc.2018.01.158
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575