Suppr超能文献

Akt信号传导及其在出生后血管新生中的作用。

Akt signaling and its role in postnatal neovascularization.

作者信息

Ma F X, Han Z C

机构信息

State Key Laboratory of Experimental Hematology and National Research Center for Stem Cell Engineering and Technology, Chinese Academy of Medical Sciences and Peking Union of Medical College, Tianjin 30020, China.

出版信息

Histol Histopathol. 2005 Jan;20(1):275-81. doi: 10.14670/HH-20.275.

Abstract

Postnatal neovascularization has been known to be involved in not only angiogenesis but also vasculogenesis. Several lines of evidence suggest a link between neovascularization and Akt, a family member of serine/threonine protein kinases. Akt phosphorylates endothelial NO synthase (eNOS) and thereby enhances endothelial NO synthesis and influences postnatal vessel growth. Akt signaling is activated by a variety of stimuli in endothelial cells and endothelial progenitor cells (EPCs). Activation of the Akt kinase orchestrates a number of signaling pathways potentially involved in angiogenesis. Dominant negative Akt overexpression leads to functional blocking of EPC bioactivity. Because neovascularization is implicated in the pathophysiology of a number of diseases and is becoming an important therapeutic strategy for those diseases, further dissection of the Akt pathway and elucidation of the downstream effector molecules will lead to a better understanding of postnatal neovascularization and may provide avenues for the development of novel therapeutic interventions. In this review, molecular mechanisms of Akt signal pathway will be discussed with special emphasis on its role in neovascularization.

摘要

已知产后新生血管形成不仅涉及血管生成,还涉及血管发生。多条证据表明新生血管形成与丝氨酸/苏氨酸蛋白激酶家族成员Akt之间存在联系。Akt使内皮型一氧化氮合酶(eNOS)磷酸化,从而增强内皮型一氧化氮的合成并影响产后血管生长。Akt信号通路在内皮细胞和内皮祖细胞(EPC)中被多种刺激激活。Akt激酶的激活协调了许多可能参与血管生成的信号通路。显性负性Akt过表达导致EPC生物活性的功能阻断。由于新生血管形成与多种疾病的病理生理学有关,并且正成为这些疾病的重要治疗策略,进一步剖析Akt途径并阐明下游效应分子将有助于更好地理解产后新生血管形成,并可能为开发新的治疗干预措施提供途径。在这篇综述中,将讨论Akt信号通路的分子机制,特别强调其在新生血管形成中的作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验