tetano
Editor, Senior Moderator
Br J Pharmacol
. 2021 Oct 10.
doi: 10.1111/bph.15670. Online ahead of print.
Pyroptosis targeting via mitochondria: An educated guess to innovate COVID-19 therapies
Aarti Singh[SUP] 1 [/SUP], Daniela Strobbe[SUP] 2 [/SUP], Michelangelo Campanella[SUP] 1 2 3 [/SUP]
Affiliations
Abstract
Pyroptosis is a specialized form of inflammatory cell death which aids the defensive response against invading pathogens. Its normally tight regulation is lost during infection by the severe acute respiratory coronavirus 2 (SARS-CoV-2), and thus, uncontrolled pyroptosis disrupts the immune system and the integrity of organs defining the critical conditions in patients with high viral load. Molecular pathways engaged downstream of the formation and stabilization of the inflammasome, which are necessary to execute the process, have been uncovered and drugs are available for their regulation. However, the pharmacology of the upstream events, which are critical to sense and interpret the initial damage by the pathogen, is far from being elucidated. This limits our capacity to identify early markers and targets to ameliorate SARS-CoV-2 linked pyroptosis. Here, we focus attention on the mitochondria and pathways leading to their dysfunction, in order to elucidate the early steps of inflammasome formation and devise tools to predict and counter pathological states induced by SARS-CoV-2.
Keywords: SARS-CoV-2; mitochondria and pharmacology; pyroptosis.
. 2021 Oct 10.
doi: 10.1111/bph.15670. Online ahead of print.
Pyroptosis targeting via mitochondria: An educated guess to innovate COVID-19 therapies
Aarti Singh[SUP] 1 [/SUP], Daniela Strobbe[SUP] 2 [/SUP], Michelangelo Campanella[SUP] 1 2 3 [/SUP]
Affiliations
- PMID: 34632567
- DOI: 10.1111/bph.15670
Abstract
Pyroptosis is a specialized form of inflammatory cell death which aids the defensive response against invading pathogens. Its normally tight regulation is lost during infection by the severe acute respiratory coronavirus 2 (SARS-CoV-2), and thus, uncontrolled pyroptosis disrupts the immune system and the integrity of organs defining the critical conditions in patients with high viral load. Molecular pathways engaged downstream of the formation and stabilization of the inflammasome, which are necessary to execute the process, have been uncovered and drugs are available for their regulation. However, the pharmacology of the upstream events, which are critical to sense and interpret the initial damage by the pathogen, is far from being elucidated. This limits our capacity to identify early markers and targets to ameliorate SARS-CoV-2 linked pyroptosis. Here, we focus attention on the mitochondria and pathways leading to their dysfunction, in order to elucidate the early steps of inflammasome formation and devise tools to predict and counter pathological states induced by SARS-CoV-2.
Keywords: SARS-CoV-2; mitochondria and pharmacology; pyroptosis.