Moccia Francesco, Negri Sharon, Faris Pawan, Perna Angelica, De Luca Antonio, Soda Teresa, Berra-Romani Roberto, Guerra Germano
Laboratory of General Physiology, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, Pavia, Italy.
Department of Medicine and Health Sciences "V. Tiberio", University of Molise, Campobasso, Italy.
Front Physiol. 2021 Jan 26;12:629119. doi: 10.3389/fphys.2021.629119. eCollection 2021.
Emerging evidence hints in favor of a life-threatening link between severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) and the cardiovascular system. SARS-CoV-2 may result in dramatic cardiovascular complications, whereas the severity of COronaVIrus Disease 2019 (COVID-19) and the incidence of fatalities tend to increase in patients with pre-existing cardiovascular complications. SARS-CoV-2 is internalized into the host cells by endocytosis and may then escape the endolysosomal system via endosomes. Two-pore channels drive endolysosomal trafficking through the release of endolysosomal Ca. Recent evidence suggested that the pharmacological inhibition of TPCs prevents Ebola virus and Middle East Respiratory Syndrome COronaVirus (MERS-CoV) entry into host cells. In this perspective, we briefly summarize the biophysical and pharmacological features of TPCs, illustrate their emerging role in the cardiovascular system, and finally present them as a reliable target to treat cardiovascular complications in COVID-19 patients.
新出现的证据表明,严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)与心血管系统之间存在危及生命的联系。SARS-CoV-2可能导致严重的心血管并发症,而在已有心血管并发症的患者中,2019冠状病毒病(COVID-19)的严重程度和死亡率往往会增加。SARS-CoV-2通过内吞作用进入宿主细胞,然后可能通过内体逃离内溶酶体系统。双孔通道通过释放内溶酶体钙来驱动内溶酶体运输。最近的证据表明,对双孔通道的药理学抑制可阻止埃博拉病毒和中东呼吸综合征冠状病毒(MERS-CoV)进入宿主细胞。从这个角度来看,我们简要总结了双孔通道的生物物理和药理学特征,阐述了它们在心血管系统中新兴的作用,最后将它们作为治疗COVID-19患者心血管并发症的可靠靶点。