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10.3389/fphys.2021.629119

http://scihub22266oqcxt.onion/10.3389/fphys.2021.629119
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suck abstract from ncbi


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pmid33574769      Front+Physiol 2021 ; 12 (ä): 629119
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  • Targeting Endolysosomal Two-Pore Channels to Treat Cardiovascular Disorders in the Novel COronaVIrus Disease 2019 #MMPMID33574769
  • Moccia F; Negri S; Faris P; Perna A; De Luca A; Soda T; Berra-Romani R; Guerra G
  • Front Physiol 2021[]; 12 (ä): 629119 PMID33574769show ga
  • 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(2+). 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.
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