Calcium promotes vascular smooth muscle cell phenotypic switching in Marfan syndrome

被引:1
作者
Yang, Yunxiao [1 ]
Xie, Enzehua [2 ]
Liu, Yuhua [1 ]
Peng, Zhan [1 ]
Yu, Cuntao [2 ]
Hua, Kun [1 ]
Yang, Xiubin [1 ]
机构
[1] Capital Med Univ, Beijing Anzhen Hosp, Dept Cardiovasc Surg, Beijing 100029, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Natl Ctr Cardiovasc Dis, Fuwai Hosp, Dept Cardiovasc Surg, Beijing 100047, Peoples R China
关键词
Marfan syndrome; Vascular smooth muscle cell; Phenotypic switching; Calcium; AORTIC-ANEURYSM; PROLIFERATION; SERCA;
D O I
10.1016/j.bbrc.2023.05.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fibrillin 1 (Fbn1) mutations cause Marfan syndrome (MFS), with aortic root dilatation, dissection, and rupture. Few studies reported the blood calcium and lipid profile of MFS, and the effect of vascular smooth muscle cell (VSMC) phenotypic switching on MFS aortic aneurysm is unclear. Here, we aimed to investigate the role of calcium-related VSMC phenotypic switching in MFS. We retrospectively collected MFS patients' clinical data, performed bioinformatics analysis to screen the enriched biological process in MFS patients and mice, and detected markers of VSMC phenotypic switching on Fbn1C1039G/ thorn mice and primary aortic vascular smooth muscle cells. We found that patients with MFS have elevated blood calcium levels and dyslipidemia. Furthermore, the calcium concentration levels were increased with age in MFS mice, accompanied by the promoted VSMC phenotypic switching, and SERCA2 contributed to maintaining the contractile phenotype of VSMCs. This study provides the first evidence that the increased calcium is associated with the promoted VSMC phenotype switching in MFS. SERCA may become a novel therapeutic target for suppressing aneurysm progression in MFS. (c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:124 / 132
页数:9
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