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揭示心脏瓣膜病理生理学的复杂性。

Unveiling the intricacies of cardiac valve pathophysiology.

作者信息

Jedrzejczyk Johannes H, Hjertensgaard Oline, Puelles Victor G, Hasenkam J Michael

机构信息

Department of Cardiothoracic and Vascular Surgery, Aarhus University Hospital, Aarhus, Denmark.

Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

出版信息

Front Cardiovasc Med. 2025 Jul 24;12:1570271. doi: 10.3389/fcvm.2025.1570271. eCollection 2025.


DOI:10.3389/fcvm.2025.1570271
PMID:40777570
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12328368/
Abstract

INTRODUCTION: Heart valves have long been regarded as uncomplicated, avascular, and passive structures. However, we hypothesise that their structure and function are complex. Therefore, we have reviewed the available literature to gain a profound understanding of their cellular composition and (patho)physiological behaviour. METHODS: A systematic search for articles related to the anatomy, histology, and physiology of heart valves was conducted using PubMed and Google Scholar, as well as a manual search of journals and websites. All publications were screened by title and abstract, and potentially eligible articles were reviewed in full text to assess their relevance. RESULTS: Cardiac valves comprise a complex, three-layered structure composed of an intricate network of cells. Valvular endothelial cells cover the atrial and ventricular sides of the valves. Valvular endothelial cells are morphologically and functionally distinct from vascular endothelial cells and play a crucial role in maintaining valve function. The three-valve layers, lamina fibrosa, spongiosa, and ventricularis, exhibit distinct biomechanical properties due to their varying extracellular matrix components and valvular interstitial cells. Valvular interstitial cells can be divided into four subtypes, each exhibiting specific cellular functions essential for normal valve physiology. However, pathological stimuli can cause aberrant activation of the valvular interstitial cells, leading to valve calcification and stenosis. CONCLUSION: The intricate interplay of cellular components within cardiac valves is vital for maintaining normal valve function and structural integrity, but also contributes to valve pathology. A holistic understanding of heart valves, integrating cellular, molecular, and neural perspectives, is needed in the future.

摘要

引言:长期以来,心脏瓣膜一直被视为结构简单、无血管且被动的结构。然而,我们推测其结构和功能是复杂的。因此,我们回顾了现有文献,以深入了解其细胞组成和(病理)生理行为。 方法:使用PubMed和谷歌学术对与心脏瓣膜解剖学、组织学和生理学相关的文章进行系统检索,并手动检索期刊和网站。所有出版物均通过标题和摘要进行筛选,对潜在符合条件的文章进行全文审查以评估其相关性。 结果:心脏瓣膜由复杂的三层结构组成,该结构由错综复杂的细胞网络构成。瓣膜内皮细胞覆盖瓣膜的心房侧和心室侧。瓣膜内皮细胞在形态和功能上与血管内皮细胞不同,在维持瓣膜功能方面起着关键作用。瓣膜的三层结构,即纤维层、海绵层和心室层,由于其细胞外基质成分和瓣膜间质细胞的不同而表现出不同的生物力学特性。瓣膜间质细胞可分为四种亚型,每种亚型都具有对正常瓣膜生理学至关重要的特定细胞功能。然而,病理刺激可导致瓣膜间质细胞异常激活,从而导致瓣膜钙化和狭窄。 结论:心脏瓣膜内细胞成分的复杂相互作用对于维持正常瓣膜功能和结构完整性至关重要,但也会导致瓣膜病变。未来需要从细胞、分子和神经等多个角度对心脏瓣膜进行全面了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff5d/12328368/6ec55289b23e/fcvm-12-1570271-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff5d/12328368/d5283342520f/fcvm-12-1570271-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff5d/12328368/efd8fb4baae3/fcvm-12-1570271-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff5d/12328368/6ec55289b23e/fcvm-12-1570271-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff5d/12328368/d5283342520f/fcvm-12-1570271-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff5d/12328368/efd8fb4baae3/fcvm-12-1570271-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff5d/12328368/6ec55289b23e/fcvm-12-1570271-g003.jpg

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本文引用的文献

[1]
Valvular Heart Disease Epidemiology.

Med Sci (Basel). 2022-6-15

[2]
2021 ESC/EACTS Guidelines for the management of valvular heart disease.

Eur Heart J. 2022-2-12

[3]
Immune Privilege of Heart Valves.

Front Immunol. 2021

[4]
2020 ACC/AHA Guideline for the Management of Patients With Valvular Heart Disease: Executive Summary: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines.

Circulation. 2021-2-2

[5]
Harnessing Mechanosensation in Next Generation Cardiovascular Tissue Engineering.

Biomolecules. 2020-10-7

[6]
Endothelial-to-Mesenchymal Transition in Calcific Aortic Valve Disease.

Acta Cardiol Sin. 2020-5

[7]
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Curr Cardiol Rev. 2020

[8]
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Physiol Rev. 2019-4-1

[9]
Correlation between valvular interstitial cell morphology and phenotypes: A novel way to detect activation.

Tissue Cell. 2018-10

[10]
Activation of human aortic valve interstitial cells by local stiffness involves YAP-dependent transcriptional signaling.

Biomaterials. 2018-7-31

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