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小窝和小窝蛋白-1作为膳食多酚预防血管内皮功能障碍的靶点。

Caveolae and caveolin-1 as targets of dietary polyphenols for protection against vascular endothelial dysfunction.

作者信息

Terao Junji

机构信息

Faculty of Medicine, Tokushima University, 3-18-15 Kuramoto-cho, Tokushima 770-8503, Japan.

出版信息

J Clin Biochem Nutr. 2024 Jul;75(1):7-16. doi: 10.3164/jcbn.24-30. Epub 2024 Mar 7.

DOI:10.3164/jcbn.24-30
PMID:39070533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11273273/
Abstract

Caveolae, consisting of caveolin-1 proteins, are ubiquitously present in endothelial cells and contribute to normal cardiovascular functions by acting as a platform for cellular signaling pathways as well as transcytosis and endocytosis. However, caveolin-1 is thought to have a proatherogenic role by inhibiting endothelial nitric oxide synthase activity and Nrf2 activation, or by promoting inflammation through NF-κB activation. Dietary polyphenols were suggested to exert anti-atherosclerotic effects by a mechanism involving the inhibition of endothelial dysfunction, by which they can regulate redox-sensitive signaling pathways in relation to NF-κB and Nrf2 activation. Some monomeric polyphenols and microbiota-derived catabolites from monomeric polyphenols or polymeric tannins might be responsible for the inhibition, because they can be transferred into the circulation from the digestive tract. Several polyphenols were reported to modulate caveolin-1 expression or its localization in caveolae. Therefore, we hypothesized that circulating polyphenols affect caveolae functions by altering its structure leading to the release of caveolin-1 from caveolae, and attenuating redox-sensitive signaling pathway-dependent caveolin-1 overexpression. Further studies using circulating polyphenols at a physiologically relevant level are necessary to clarify the mechanism of action of dietary polyphenols targeting caveolae and caveolin-1.

摘要

小窝由小窝蛋白-1组成,普遍存在于内皮细胞中,并通过作为细胞信号通路以及转胞吞作用和内吞作用的平台,对正常心血管功能发挥作用。然而,小窝蛋白-1被认为具有促动脉粥样硬化作用,其机制包括抑制内皮型一氧化氮合酶活性和Nrf2激活,或通过NF-κB激活促进炎症。膳食多酚被认为通过抑制内皮功能障碍的机制发挥抗动脉粥样硬化作用,通过这种机制它们可以调节与NF-κB和Nrf2激活相关的氧化还原敏感信号通路。一些单体多酚以及来自单体多酚或聚合单宁的微生物衍生分解产物可能是这种抑制作用的原因,因为它们可以从消化道转移到循环系统中。据报道,几种多酚可调节小窝蛋白-1的表达或其在小窝中的定位。因此,我们假设循环中的多酚通过改变小窝结构,导致小窝蛋白-1从小窝中释放,并减弱氧化还原敏感信号通路依赖性小窝蛋白-1的过表达,从而影响小窝功能。有必要使用生理相关水平的循环多酚进行进一步研究,以阐明膳食多酚靶向小窝和小窝蛋白-1的作用机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce8e/11273273/9daf90dee8f8/jcbn24-30f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce8e/11273273/09828a1fbd51/jcbn24-30f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce8e/11273273/7db7d64bdb8f/jcbn24-30f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce8e/11273273/565cf3b5c62f/jcbn24-30f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce8e/11273273/9daf90dee8f8/jcbn24-30f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce8e/11273273/09828a1fbd51/jcbn24-30f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce8e/11273273/7db7d64bdb8f/jcbn24-30f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce8e/11273273/565cf3b5c62f/jcbn24-30f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce8e/11273273/9daf90dee8f8/jcbn24-30f04.jpg

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