Smooth Muscle Heterogeneity and Plasticity in Health and Aortic Aneurysmal Disease

被引:18
作者
Hu, Yunwen [1 ]
Cai, Zhaohua [1 ]
He, Ben [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Cardiol, Sch Med, Shanghai 200030, Peoples R China
基金
中国国家自然科学基金;
关键词
abdominal aortic aneurysm; thoracic aortic aneurysm; VSMC; phenotypic switching; MESENCHYMAL STEM-CELLS; EXTRACELLULAR-MATRIX; TGFBR2; MUTATIONS; PROGENITOR CELLS; ASCENDING AORTA; BLOOD-FLOW; PHENOTYPIC MODULATION; THORACIC AORTA; C-MYB; GROWTH;
D O I
10.3390/ijms241411701
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
Vascular smooth muscle cells (VSMCs) are the predominant cell type in the medial layer of the aorta, which plays a critical role in the maintenance of aortic wall integrity. VSMCs have been suggested to have contractile and synthetic phenotypes and undergo phenotypic switching to contribute to the deteriorating aortic wall structure. Recently, the unprecedented heterogeneity and diversity of VSMCs and their complex relationship to aortic aneurysms (AAs) have been revealed by high-resolution research methods, such as lineage tracing and single-cell RNA sequencing. The aortic wall consists of VSMCs from different embryonic origins that respond unevenly to genetic defects that directly or indirectly regulate VSMC contractile phenotype. This difference predisposes to hereditary AAs in the aortic root and ascending aorta. Several VSMC phenotypes with different functions, for example, secreting VSMCs, proliferative VSMCs, mesenchymal stem cell-like VSMCs, immune-related VSMCs, proinflammatory VSMCs, senescent VSMCs, and stressed VSMCs are identified in non-hereditary AAs. The transformation of VSMCs into different phenotypes is an adaptive response to deleterious stimuli but can also trigger pathological remodeling that exacerbates the pathogenesis and development of AAs. This review is intended to contribute to the understanding of VSMC diversity in health and aneurysmal diseases. Papers that give an update on VSMC phenotype diversity in health and aneurysmal disease are summarized and recent insights on the role of VSMCs in AAs are discussed.
引用
收藏
页数:22
相关论文
共 183 条
[1]   Transcription factor GATA6 promotes migration of human coronary artery smooth muscle cells in vitro [J].
Alajbegovic, Azra ;
Daoud, Fatima ;
Ali, Neserin ;
Kawka, Katarzyna ;
Holmberg, Johan ;
Albinsson, Sebastian .
FRONTIERS IN PHYSIOLOGY, 2022, 13
[2]   Smooth muscle cell fate and plasticity in atherosclerosis [J].
Allahverdian, Sima ;
Chaabane, Chiraz ;
Boukais, Kamel ;
Francis, Gordon A. ;
Bochaton-Piallat, Marie-Luce .
CARDIOVASCULAR RESEARCH, 2018, 114 (04) :540-550
[3]   TGF-β (Transforming Growth Factor-β) Signaling Protects the Thoracic and Abdominal Aorta From Angiotensin II-Induced Pathology by Distinct Mechanisms [J].
Angelov, Stoyan N. ;
Hu, Jie Hong ;
Wei, Hao ;
Airhart, Nathan ;
Shi, Minghui ;
Dichek, David A. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2017, 37 (11) :2102-+
[4]   Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD) [J].
Arnaud, Pauline ;
Hanna, Nadine ;
Benarroch, Louise ;
Aubart, Melodie ;
Bal, Laurence ;
Bouvagnet, Patrice ;
Busa, Tiffany ;
Dulac, Yves ;
Dupuis-Girod, Sophie ;
Edouard, Thomas ;
Faivre, Laurence ;
Gouya, Laurent ;
Lacombe, Didier ;
Langeois, Maud ;
Leheup, Bruno ;
Milleron, Olivier ;
Naudion, Sophie ;
Odent, Sylvie ;
Tchitchinadze, Maria ;
Ropers, Jacques ;
Jondeau, Guillaume ;
Boileau, Catherine .
GENETICS IN MEDICINE, 2019, 21 (09) :2015-2024
[5]   Pathophysiology and Therapeutics of Thoracic Aortic Aneurysm in Marfan Syndrome [J].
Asano, Keiichi ;
Cantalupo, Anna ;
Sedes, Lauriane ;
Ramirez, Francesco .
BIOMOLECULES, 2022, 12 (01)
[6]   Genomic insights in ascending aortic size and distensibility [J].
Benjamins, Jan Walter ;
Yeung, Ming Wai ;
van de Vegte, Yordi J. ;
Said, M. Abdullah ;
van der Linden, Thijs ;
Ties, Daan ;
Juarez-Orozco, Luis E. ;
Verweij, Niek ;
van der Harst, Pim .
EBIOMEDICINE, 2022, 75
[7]   Novel concepts for the role of smooth muscle cells in vascular disease: towards a new smooth muscle cell classification [J].
Bochaton-Piallat, Marie-Luce ;
Back, Magnus .
CARDIOVASCULAR RESEARCH, 2018, 114 (04) :477-480
[8]   Abdominal Aortic Aneurysm Genetic Associations: Mostly False? A Systematic Review and Meta-analysis [J].
Bradley, D. T. ;
Badger, S. A. ;
McFarland, M. ;
Hughes, A. E. .
EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY, 2016, 51 (01) :64-75
[9]   Postnatal Smad3 Inactivation in Murine Smooth Muscle Cells Elicits a Temporally and Regionally Distinct Transcriptional Response [J].
Bramel, Emily E. ;
Creamer, Tyler J. ;
Saqib, Muzna ;
Nunez, Wendy A. Camejo ;
Bagirzadeh, Rustam ;
Roker, LaToya Ann ;
Goff, Loyal A. ;
MacFarlane, Elena Gallo .
FRONTIERS IN CARDIOVASCULAR MEDICINE, 2022, 9
[10]   Phenotypic alteration of vascular smooth muscle cells precedes elastolysis in a mouse model of Marfan syndrome [J].
Bunton, TE ;
Biery, NJ ;
Myers, L ;
Gayraud, B ;
Ramirez, F ;
Dietz, HC .
CIRCULATION RESEARCH, 2001, 88 (01) :37-43