血管生物学及其他领域中的 KRIT1。

IF 3.8 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Bioscience Reports Pub Date : 2024-07-31 DOI:10.1042/BSR20231675
Angela J Glading
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引用次数: 0

摘要

KRIT1 是一种 75 kDa 的支架蛋白,它通过限制对炎症刺激的反应以及维持静止和稳定的内皮屏障来调节内皮细胞的表型。KRIT1 的功能缺失突变会导致脑海绵畸形(CCM)的发生,这种疾病的特征是形成异常血管,表现出屏障功能丧失、内皮细胞增殖增加和基因表达改变。虽然我们对 KRIT1 以及与之功能相关的蛋白 CCM2 和 PDCD10 如何调控血管和血管屏障的认识取得了许多进展,但仍存在一些重要的未决问题。此外,KRIT1 被广泛表达,而且 KRIT1 和其他 CCM 蛋白已被证明在非内皮细胞类型和组织中发挥重要作用,这可能与它们作为 CCM 致病源的作用有关,也可能无关。在这篇综述中,我们将讨论有关 KRIT1 在血管生理学中作用的一些悬而未决的问题,并讨论最近的研究进展,这些进展表明这种普遍表达的蛋白可能在内皮细胞之外也有作用。
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KRIT1 in vascular biology and beyond.

KRIT1 is a 75 kDa scaffolding protein which regulates endothelial cell phenotype by limiting the response to inflammatory stimuli and maintaining a quiescent and stable endothelial barrier. Loss-of-function mutations in KRIT1 lead to the development of cerebral cavernous malformations (CCM), a disease marked by the formation of abnormal blood vessels which exhibit a loss of barrier function, increased endothelial proliferation, and altered gene expression. While many advances have been made in our understanding of how KRIT1, and the functionally related proteins CCM2 and PDCD10, contribute to the regulation of blood vessels and the vascular barrier, some important open questions remain. In addition, KRIT1 is widely expressed and KRIT1 and the other CCM proteins have been shown to play important roles in non-endothelial cell types and tissues, which may or may not be related to their role as pathogenic originators of CCM. In this review, we discuss some of the unsettled questions regarding the role of KRIT1 in vascular physiology and discuss recent advances that suggest this ubiquitously expressed protein may have a role beyond the endothelial cell.

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来源期刊
Bioscience Reports
Bioscience Reports 生物-细胞生物学
CiteScore
8.50
自引率
0.00%
发文量
380
审稿时长
6-12 weeks
期刊介绍: Bioscience Reports provides a home for sound scientific research in all areas of cell biology and molecular life sciences. Since 2012, Bioscience Reports has been fully Open Access and publishes all papers under the liberal CC BY licence, giving the life science community quality research to share and discuss.Content before 2012 is subscription-only, and is accessible via archive purchase. Articles are assessed on soundness, providing a home for valid findings and data. We welcome papers that span disciplines (e.g. chemistry, medicine), including papers describing: -new methodologies -tools and reagents to probe biological questions -mechanistic details -disease mechanisms -metabolic processes and their regulation -structure and function -bioenergetics
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