血管重构过程中血管同一性的改变

Q3 Medicine
Yukihiko Aoyagi MD , Andrew W. Schwartz BS , Zhuo Li MD, PhD , Hualong Bai MD, PhD , Luis Gonzalez PhD , Cayetana Lazcano Etchebarne BS , Yuichi Ohashi MD , Masaki Kano MD , Bryan Ho MD , Kathleen Martin PhD , Alan Dardik MD, PhD
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引用次数: 0

摘要

血管重构是一个动态过程,其特征是血管特性的改变,从而影响血管的结构和功能。分子标记确定细胞身份为动脉、静脉和淋巴管:Ephrin-B2和Notch决定动脉身份,EphB4和COUP-TFII决定静脉身份,Prox1决定淋巴身份。方法对实验文献进行综述。结果这些蛋白在第一次心跳前的发育过程中决定身份。成年期血液动力学的改变也会改变血管的特性。身份标记的变化与血管细胞表型或疾病的变化一致,因此可能在调节正常和病理血管重塑中发挥作用。血管疾病如动静脉畸形和肺动脉高压是由细胞表型和血管特性的改变驱动的。手术干预,如动静脉瘘(AVF)的创建和动脉搭桥使用静脉移植物诱导身份的改变;静脉移植物失去了静脉身份,但不获得动脉身份,而AVF的静脉肢体在获得动脉身份的同时保留了静脉身份。血管贴片成形术后,血管贴片在其环境中重塑。静脉环境中的斑块获得静脉身份,动脉环境中的斑块形成动脉身份。有趣的是,AVF静脉流出处的斑块呈现静脉-动脉混合表型。结论血管身份的改变在生理和病理条件下驱动血管重构,对血管疾病的治疗策略具有潜在的指导意义。血管重构对于血管的生理和病理适应都是必不可少的。在发育过程中、疾病状态中以及手术和血管内干预后,血管特性的改变是对血流动力学力的反应,并介导血管重构。动脉和静脉身份分子标记的改变调节细胞表型、细胞外基质和血管壁结构,最终决定血管的长期功能。了解控制血管身份的分子调控途径有助于了解血管重塑的机制,并可能确定治疗血管疾病的潜在治疗靶点,改善血管干预后的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Changes in vascular identity during vascular remodeling

Changes in vascular identity during vascular remodeling

Background

Vascular remodeling is a dynamic process characterized by changes in vascular identity that impact vessel structure and function. Molecular markers define cellular identity as arteries, veins, and lymphatic vessels: Ephrin-B2 and Notch determine arterial identity, EphB4 and COUP-TFII determine venous identity, and Prox1 determines lymphatic identity.

Methods

This is a review of experimental literature.

Results

These proteins determine identity during development before the first heartbeat. Hemodynamic changes in adulthood can also alter vascular identity. Changes in identity markers coincide with changes in vascular cell phenotype or disease and thus may play a role in regulating both normal and pathological vascular remodeling. Vascular diseases such as arteriovenous malformations and pulmonary hypertension are driven by changes in cell phenotype and vessel identity. Surgical interventions such as arteriovenous fistula (AVF) creation and arterial bypass using vein grafts induce alterations in identity; vein grafts lose their venous identity, but do not acquire arterial identity, whereas venous limbs of AVF gain arterial identity while retaining their venous identity. After patch angioplasty, vascular patches remodel in their environment. Patches in the venous environment acquire venous identity and patches in the arterial environment develop arterial identity. Interestingly, patches in the venous outflow of AVF gain a mixed venous-arterial phenotype.

Conclusions

Changes in vascular identity drive vascular remodeling in both physiological and pathological settings, with potential implications for therapeutic strategies targeting vascular diseases.

Clinical Relevance

Vascular remodeling is essential for both physiological and pathological vascular adaptation. Changes in vascular identity occur in response to hemodynamic forces and mediate vascular remodeling during development, in disease states, and after surgical and endovascular interventions. Alterations in arterial and venous molecular markers of identity regulate cellular phenotype, the extracellular matrix, and vessel wall structure, ultimately determining long-term vessel function. Understanding the molecular regulatory pathways controlling vascular identity provides insight into understanding the mechanisms of vascular remodeling and may identify potential therapeutic targets to treat vascular disease and improve outcomes after vascular interventions.
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来源期刊
CiteScore
4.20
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