| Literature DB >> 33574769 |
Francesco Moccia1, Sharon Negri1, Pawan Faris1, Angelica Perna2, Antonio De Luca3, Teresa Soda4, Roberto Berra-Romani5, Germano Guerra2.
Abstract
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 Ca2+. 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.Entities:
Keywords: 5)P2; COVID-19; NAADP; PI(3; SARS-CoV-2; cardiovascular system; endolysosomal Ca2+ signaling; two-pore channels
Year: 2021 PMID: 33574769 PMCID: PMC7870486 DOI: 10.3389/fphys.2021.629119
Source DB: PubMed Journal: Front Physiol ISSN: 1664-042X Impact factor: 4.566