Li Sanjun, Xiao Xiaoyong, Chang Yuechen, Xu Ziyao, Zheng Xianping, Zhou Haiwen, Ding Haiqiang, Lu Weiling, Li Tian, Tao Yu
Department of Cardiology, Jiangxi Provincial People's Hospital, the First Affiliated Hospital of Nanchang Medical College, Nanchang, China.
Department of Emergency Medicine, The First Affiliated Hospital of Shenzhen University, Health Science Center, Shenzhen Second People's Hospital, Shenzhen, Guangdong, China.
J Cell Mol Med. 2025 Apr;29(7):e70509. doi: 10.1111/jcmm.70509.
Abdominal aortic aneurysm (AAA) is a life-threatening disease featuring extensive membrane destruction in the vascular wall, which is closely associated with the phenotypic switching of vascular smooth muscle cells (VSMC). A thorough understanding of the changes in regulatory factors during the pathogenesis of VSMC phenotypic switching is essential for medical treatments in AAA. NRF2 was deemed to hold a pivotal position in developing AAA, especially as it can regulate VSMC phenotypic switching. In this study, we found that berberine prevents the formation of AAA by regulating the phenotypic switching of VSMC, which was well validated in both in vitro and in vivo functional experiments. Mechanically, we found that berberine regulates VSMC phenotypic switching by promoting the expression of downstream VSMC contraction genes through the deubiquitination of Keap1, in which the deubiquitinating enzyme USP15 plays an important mediating role in this process.
腹主动脉瘤(AAA)是一种危及生命的疾病,其特征是血管壁出现广泛的膜破坏,这与血管平滑肌细胞(VSMC)的表型转换密切相关。深入了解VSMC表型转换发病机制中调节因子的变化对于AAA的医学治疗至关重要。NRF2被认为在AAA的发展中占据关键地位,特别是因为它可以调节VSMC表型转换。在本研究中,我们发现黄连素通过调节VSMC的表型转换来预防AAA的形成,这在体外和体内功能实验中均得到了充分验证。从机制上讲,我们发现黄连素通过Keap1的去泛素化促进下游VSMC收缩基因的表达来调节VSMC表型转换,其中去泛素化酶USP15在此过程中起重要介导作用。