Zhang Qi, Pavlinov Ivan, Ye Yihong, Zheng Wei
Therapeutic Development Branch, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, United States.
Laboratory of Molecular Biology, National Institute of Diabetes, Digestive, and Kidney Diseases, National Institutes of Health, Bethesda, MD, United States.
Front Med (Lausanne). 2024 Mar 27;11:1364657. doi: 10.3389/fmed.2024.1364657. eCollection 2024.
The global pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has led to an urgent need for effective therapeutic options. SARS-CoV-2 is a novel coronavirus responsible for the COVID-19 pandemic that has resulted in significant morbidity and mortality worldwide. The virus is known to enter host cells by binding to the angiotensin-converting enzyme 2 (ACE2) receptor, and emerging evidence suggests that heparan sulfate proteoglycans (HSPGs) play a crucial role in facilitating this process. HSPGs are abundant cell surface proteoglycan present in many tissues, including the lung, and have been shown to interact directly with the spike protein of SARS-CoV-2. This review aims to summarize the current understanding of the role of HSPGs in SARS-CoV-2 infection and the potential of developing new therapies targeting HSPGs.
由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的全球大流行导致迫切需要有效的治疗选择。SARS-CoV-2是一种新型冠状病毒,导致了全球范围内的COVID-19大流行,造成了重大的发病率和死亡率。已知该病毒通过与血管紧张素转换酶2(ACE2)受体结合进入宿主细胞,新出现的证据表明硫酸乙酰肝素蛋白聚糖(HSPGs)在促进这一过程中起关键作用。HSPGs是许多组织(包括肺)中丰富的细胞表面蛋白聚糖,已被证明可直接与SARS-CoV-2的刺突蛋白相互作用。本综述旨在总结目前对HSPGs在SARS-CoV-2感染中的作用的理解以及开发针对HSPGs的新疗法的潜力。