Liao Yi-En, Liu Jian, Arnold Katelyn
Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, United States.
Front Mol Biosci. 2023 Feb 14;10:1146685. doi: 10.3389/fmolb.2023.1146685. eCollection 2023.
Heparan sulfates (HSs) are the main components in the glycocalyx which covers endothelial cells and modulates vascular homeostasis through interactions with multiple Heparan sulfate binding proteins (HSBPs). During sepsis, heparanase increases and induces HS shedding. The process causes glycocalyx degradation, exacerbating inflammation and coagulation in sepsis. The circulating heparan sulfate fragments may serve as a host defense system by neutralizing dysregulated Heparan sulfate binding proteins or pro-inflammatory molecules in certain circumstances. Understanding heparan sulfates and heparan sulfate binding proteins in health and sepsis is critical to decipher the dysregulated host response in sepsis and advance drug development. In this review, we will overview the current understanding of HS in glycocalyx under septic condition and the dysfunctional heparan sulfate binding proteins as potential drug targets, particularly, high mobility group box 1 (HMGB1) and histones. Moreover, several drug candidates based on heparan sulfates or related to heparan sulfates, such as heparanase inhibitors or heparin-binding protein (HBP), will be discussed regarding their recent advances. By applying chemical or chemoenzymatic approaches, the structure-function relationship between heparan sulfates and heparan sulfate binding proteins is recently revealed with structurally defined heparan sulfates. Such homogenous heparan sulfates may further facilitate the investigation of the role of heparan sulfates in sepsis and the development of carbohydrate-based therapy.
硫酸乙酰肝素(HSs)是覆盖在内皮细胞表面的糖萼的主要成分,通过与多种硫酸乙酰肝素结合蛋白(HSBPs)相互作用来调节血管稳态。在脓毒症期间,肝素酶增加并诱导HS脱落。这一过程导致糖萼降解,加剧脓毒症中的炎症和凝血。在某些情况下,循环中的硫酸乙酰肝素片段可通过中和失调的硫酸乙酰肝素结合蛋白或促炎分子,作为一种宿主防御系统。了解健康和脓毒症状态下的硫酸乙酰肝素及硫酸乙酰肝素结合蛋白,对于解读脓毒症中失调的宿主反应及推进药物研发至关重要。在本综述中,我们将概述目前对脓毒症状态下糖萼中HS的理解,以及作为潜在药物靶点的功能失调的硫酸乙酰肝素结合蛋白,特别是高迁移率族蛋白B1(HMGB1)和组蛋白。此外,还将讨论几种基于硫酸乙酰肝素或与硫酸乙酰肝素相关的候选药物,如肝素酶抑制剂或肝素结合蛋白(HBP),以及它们的最新进展。通过应用化学或化学酶法,最近利用结构明确的硫酸乙酰肝素揭示了硫酸乙酰肝素与硫酸乙酰肝素结合蛋白之间的结构-功能关系。这种同质的硫酸乙酰肝素可能进一步促进对硫酸乙酰肝素在脓毒症中的作用的研究以及基于碳水化合物疗法的开发。