Division of Cardiology, Department of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430000, China.
Department of Orthopedics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430000, China.
Biochem Soc Trans. 2021 Feb 26;49(1):485-494. doi: 10.1042/BST20200981.
Valosin-containing protein (VCP/p97) is a member of the conserved type II AAA+ (ATPases associated with diverse cellular activities) family of proteins with multiple biological functions, especially in protein homeostasis. Mutations in VCP/p97 are reportedly related to unique autosomal dominant diseases, which may worsen cardiac function. Although the structure of VCP/p97 has been clearly characterized, with reports of high abundance in the heart, research focusing on the molecular mechanisms underpinning the roles of VCP/p97 in the cardiovascular system has been recently undertaken over the past decades. Recent studies have shown that VCP/p97 deficiency affects myocardial fibers and induces heart failure, while overexpression of VCP/p97 eliminates ischemia/reperfusion injury and relieves pathological cardiac hypertrophy caused by cardiac pressure overload, which is related to changes in the mitochondria and calcium overload. However, certain studies have drawn opposing conclusions, including the mitigation of ischemia/reperfusion injury via inhibition of VCP/p97 ATPase activity. Nevertheless, these emerging studies shed light on the role of VCP/p97 and its therapeutic potential in cardiovascular diseases. In other words, VCP/p97 may be involved in the development of cardiovascular disease, and is anticipated to be a new therapeutic target. This review summarizes current findings regarding VCP/p97 in the cardiovascular system for the first time, and discusses the role of VCP/p97 in cardiovascular disease.
泛素结合酶 p97(VCP/p97)是具有多种生物学功能的保守 II 型 AAA+(与多种细胞活动相关的 ATP 酶)家族蛋白的成员,尤其在蛋白质稳态中。VCP/p97 的突变与独特的常染色体显性疾病有关,可能会导致心脏功能恶化。尽管 VCP/p97 的结构已被明确描述,且在心脏中含量丰富,但过去几十年来,研究人员才开始关注 VCP/p97 在心血管系统中的分子机制。最近的研究表明,VCP/p97 缺乏会影响心肌纤维并导致心力衰竭,而过表达 VCP/p97 可消除缺血/再灌注损伤并缓解由心脏压力超负荷引起的病理性心肌肥厚,这与线粒体和钙超载的变化有关。然而,某些研究得出了相反的结论,包括通过抑制 VCP/p97 ATP 酶活性减轻缺血/再灌注损伤。尽管如此,这些新兴研究阐明了 VCP/p97 在心血管疾病中的作用及其治疗潜力。换句话说,VCP/p97 可能参与了心血管疾病的发生发展,有望成为新的治疗靶点。本综述首次总结了 VCP/p97 在心血管系统中的研究现状,并讨论了 VCP/p97 在心血管疾病中的作用。