Inomata Yui, Nagasaka Shouta, Miyate Kazuki, Goto Yuta, Hino Chizuru, Toukairin Chihiro, Higashio Rieko, Ishida Kinji, Saino Tomoyuki, Hirose Masamichi, Tsumura Hideki, Sanbe Atsushi
Department of Pharmacotherapeutics, School of Pharmacy, Iwate Medical University, Iwate 028-3694, Japan.
The Center for Electron Microscopy & Bio-imaging Research, Central Research Laboratories, Iwate Medical University, Morioka, Iwate 028-3694, Japan.
Biochem Biophys Res Commun. 2018 Feb 19;496(4):1141-1147. doi: 10.1016/j.bbrc.2018.01.158. Epub 2018 Jan 31.
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.
Bcl-2相关抗凋亡基因3(BAG3)在心肌和骨骼肌中均有强烈表达。最近的一项研究表明,BAG3可能在肌肉中发挥保护作用。然而,关于BAG3在心肌中的具体作用,人们了解甚少。为了更好地理解心脏中BAG3的功能作用,我们构建了过表达BAG3的转基因(TG)小鼠。在BAG3转基因小鼠中观察到缩短分数降低以及心钠素的诱导。此外,在BAG3转基因小鼠心脏中检测到小热休克蛋白(small HSPs)的蛋白质水平显著降低。我们分析了在BAG3转基因小鼠中抑制泛素-蛋白酶体系统(UPS)或自噬系统(AS)时心脏小热休克蛋白的水平。在BAG3转基因小鼠心脏中,自噬系统对小热休克蛋白的蛋白质周转有激活作用。因此,BAG3通过激活心脏中的自噬对小热休克蛋白的蛋白质周转至关重要。