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二叶式主动脉瓣患者升主动脉中的内皮/上皮间质转化

Endothelial/Epithelial Mesenchymal Transition in Ascending Aortas of Patients With Bicuspid Aortic Valve.

作者信息

Maleki Shohreh, Poujade Flore-Anne, Bergman Otto, Gådin Jesper R, Simon Nancy, Lång Karin, Franco-Cereceda Anders, Body Simon C, Björck Hanna M, Eriksson Per

机构信息

Cardiovascular Medicine Unit, Center for Molecular Medicine, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Solna, Sweden.

Cardiothoracic Surgery Unit, Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, Solna, Sweden.

出版信息

Front Cardiovasc Med. 2019 Dec 17;6:182. doi: 10.3389/fcvm.2019.00182. eCollection 2019.

Abstract

Thoracic aortic aneurysm (TAA) is the progressive enlargement of the aorta due to destructive changes in the connective tissue of the aortic wall. Aneurysm development is silent and often first manifested by the drastic events of aortic dissection or rupture. As yet, therapeutic agents that halt or reverse the process of aortic wall deterioration are absent, and the only available therapeutic recommendation is elective prophylactic surgical intervention. Being born with a bicuspid instead of the normal tricuspid aortic valve (TAV) is a major risk factor for developing aneurysm in the ascending aorta later in life. Although the pathophysiology of the increased aneurysm susceptibility is not known, recent studies are suggestive of a transformation of aortic endothelium into a more mesenchymal state i.e., an endothelial-to-mesenchymal transition in these individuals. This process involves the loss of endothelial cell features, resulting in junction instability and enhanced vascular permeability of the ascending aorta that may lay the ground for increased aneurysm susceptibility. This finding differentiates and further emphasizes the specific characteristics of aneurysm development in individuals with a bicuspid aortic valve (BAV). This review discusses the possibility of a developmental fate shared between the aortic endothelium and aortic valves. It further speculates about the impact of aortic endothelium phenotypic shift on aneurysm development in individuals with a BAV and revisits previous studies in the light of the new findings.

摘要

胸主动脉瘤(TAA)是由于主动脉壁结缔组织的破坏性改变导致主动脉逐渐扩张。动脉瘤的发展是隐匿的,通常首先表现为主动脉夹层或破裂等严重事件。目前,尚无能够阻止或逆转主动脉壁恶化进程的治疗药物,唯一可行的治疗建议是选择性预防性手术干预。出生时患有二叶式而非正常的三叶式主动脉瓣(TAV)是日后发生升主动脉瘤的主要危险因素。尽管动脉瘤易感性增加的病理生理学尚不清楚,但最近的研究表明,这些个体的主动脉内皮细胞会转变为更具间充质特性的状态,即发生内皮-间充质转化。这一过程涉及内皮细胞特征的丧失,导致升主动脉的连接不稳定和血管通透性增强,这可能是动脉瘤易感性增加的基础。这一发现区分并进一步强调了二叶式主动脉瓣(BAV)个体动脉瘤发展的特定特征。本综述讨论了主动脉内皮细胞和主动脉瓣之间可能存在的共同发育命运。它进一步推测了主动脉内皮细胞表型转变对BAV个体动脉瘤发展的影响,并根据新发现重新审视了以往的研究。

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