丝氨酸
发病机制
机制(生物学)
疾病
功能(生物学)
细胞生物学
苏氨酸
限制
医学
生物信息学
生物
药理学
酶
生物化学
免疫学
内科学
哲学
工程类
认识论
机械工程
作者
Israel Olapeju Bolanle,Kirsten Riches-Suman,Richard A. Williamson,Timothy M. Palmer
标识
DOI:10.1016/j.phrs.2021.105467
摘要
Cardiovascular diseases (CVDs) are the leading cause of death globally. While the major focus of pharmacological and non-pharmacological interventions has been on targeting disease pathophysiology and limiting predisposing factors, our understanding of the cellular and molecular mechanisms underlying the pathogenesis of CVDs remains incomplete. One mechanism that has recently emerged is protein O-GlcNAcylation. This is a dynamic, site-specific reversible post-translational modification of serine and threonine residues on target proteins and is controlled by two enzymes: O-linked β-N-acetylglucosamine transferase (OGT) and O-linked β-N-acetylglucosaminidase (OGA). Protein O-GlcNAcylation alters the cellular functions of these target proteins which play vital roles in pathways that modulate vascular homeostasis and cardiac function. Through this review, we aim to give insights on the role of protein O-GlcNAcylation in cardiovascular diseases and identify potential therapeutic targets in this pathway for development of more effective medicines to improve patient outcomes.
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