Department of Clinical Sciences Lund, Oncology, Lund University, Lund, Sweden.
Department of Immunology, Genetics, and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Am J Physiol Cell Physiol. 2023 Jan 1;324(1):C76-C84. doi: 10.1152/ajpcell.00453.2022. Epub 2022 Dec 2.
As structural components of the glycocalyx, heparan sulfate proteoglycans (HSPGs) are involved in multiple pathophysiological processes at the apex of cell signaling cascades, and as endocytosis receptors for particle structures, such as lipoproteins, extracellular vesicles, and enveloped viruses, including SARS-CoV-2. Given their diversity and complex biogenesis regulation, HSPGs remain understudied. Here we compile some of the latest studies focusing on HSPGs as internalizing receptors of extracellular vesicles ("endogenous virus") and SARS-CoV-2 lipid-enclosed particles and highlight similarities in their biophysical and structural characteristics. Specifically, the similarities in their biogenesis, size, and lipid composition may explain a common dependence on HSPGs for efficient cell-surface attachment and uptake. We further discuss the relative complexity of extracellular vesicle composition and the viral mechanisms that evolve towards increased infectivity that complicate therapeutic strategies addressing blockade of their uptake.
作为糖萼的结构成分,硫酸乙酰肝素蛋白聚糖(HSPGs)参与细胞信号级联反应的顶端的多种病理生理过程,并且作为脂蛋白、细胞外囊泡和包膜病毒(包括 SARS-CoV-2)等颗粒结构的内吞受体。鉴于其多样性和复杂的生物发生调节,HSPGs 的研究仍不够充分。在这里,我们汇集了一些最新的研究,重点关注 HSPGs 作为细胞外囊泡(“内源性病毒”)和 SARS-CoV-2 脂质包被颗粒的内吞受体,并强调它们在生物物理和结构特征上的相似性。具体来说,它们在生物发生、大小和脂质组成上的相似性可能解释了它们对 HSPGs 高效细胞表面附着和摄取的共同依赖性。我们进一步讨论了细胞外囊泡组成的相对复杂性以及病毒进化为提高感染性的机制,这使得针对阻断其摄取的治疗策略变得复杂。