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10.1152/ajpcell.00224.2020 http://scihub22266oqcxt.onion/10.1152/ajpcell.00224.2020 32510973!7381712!32510973     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=32510973&cmd=llinks): Failed to open stream: HTTP request failed! 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Decoding SARS-CoV-2 hijacking of host mitochondria in COVID-19 pathogenesis |pdf=|usr=}}{{32510973}} gab.com Text Decoding SARS-CoV-2 hijacking of host mitochondria in COVID-19 pathogenesis JO: Am J Physiol Cell Physiol http://www.kidney.de/pget.php?&tw=1&pmid=32510973 #FOAvip Because of the ongoing pandemic around the world, the mechanisms underlying the SARS-CoV-2-induced COVID-19 are subject to intense investigation. Based on available data for the SARS-CoV-1 virus, we suggest how CoV-2 localization of RNA transcripts in mitochondria hijacks the host cell's mitochondrial function to viral advantage. Besides viral RNA transcripts, RNA also localizes to mitochondria. SARS-CoV-2 may manipulate mitochondrial function indirectly, first by ACE2 regulation of mitochondrial function, and once it enters the host cell, open-reading frames (ORFs) such as ORF-9b can directly manipulate mitochondrial function to evade host cell immunity and facilitate virus replication and COVID-19 disease. Manipulations of host mitochondria by viral ORFs can release mitochondrial DNA (mtDNA) in the cytoplasm and activate mtDNA-induced inflammasome and suppress innate and adaptive immunity. We argue that a decline in ACE2 function in aged individuals, coupled with the age-associated decline in mitochondrial functions resulting in chronic metabolic disorders like diabetes or cancer, may make the host more vulnerable to infection and health complications to mortality. These observations suggest that distinct localization of viral RNA and proteins in mitochondria must play essential roles in SARS-CoV-2 pathogenesis. Understanding the mechanisms underlying virus communication with host mitochondria may provide critical insights into COVID-19 pathologies. An investigation into the SARS-CoV-2 hijacking of mitochondria should lead to novel approaches to prevent and treat COVID-19. Twit Text FOAVip Decoding SARS-CoV-2 hijacking of host mitochondria in COVID-19 pathogenesis ????Am J Physiol Cell Physiol http://www.kidney.de/pget.php?&tw=1&pmid=32510973 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32510973 #FOAvip English Wikipedia <ref>{{Cite pmid|32510973}}</ref> Decoding SARS-CoV-2 hijacking of host mitochondria in COVID-19 pathogenesis #MMPMID32510973 Singh KK; Chaubey G; Chen JY; Suravajhala P Am J Physiol Cell Physiol 2020[Aug]; 319 (2): C258-C267 PMID32510973show ga Because of the ongoing pandemic around the world, the mechanisms underlying the SARS-CoV-2-induced COVID-19 are subject to intense investigation. Based on available data for the SARS-CoV-1 virus, we suggest how CoV-2 localization of RNA transcripts in mitochondria hijacks the host cell's mitochondrial function to viral advantage. Besides viral RNA transcripts, RNA also localizes to mitochondria. SARS-CoV-2 may manipulate mitochondrial function indirectly, first by ACE2 regulation of mitochondrial function, and once it enters the host cell, open-reading frames (ORFs) such as ORF-9b can directly manipulate mitochondrial function to evade host cell immunity and facilitate virus replication and COVID-19 disease. Manipulations of host mitochondria by viral ORFs can release mitochondrial DNA (mtDNA) in the cytoplasm and activate mtDNA-induced inflammasome and suppress innate and adaptive immunity. We argue that a decline in ACE2 function in aged individuals, coupled with the age-associated decline in mitochondrial functions resulting in chronic metabolic disorders like diabetes or cancer, may make the host more vulnerable to infection and health complications to mortality. These observations suggest that distinct localization of viral RNA and proteins in mitochondria must play essential roles in SARS-CoV-2 pathogenesis. Understanding the mechanisms underlying virus communication with host mitochondria may provide critical insights into COVID-19 pathologies. An investigation into the SARS-CoV-2 hijacking of mitochondria should lead to novel approaches to prevent and treat COVID-19. |Adaptive Immunity[MESH] |Angiotensin-Converting Enzyme 2[MESH] |Animals[MESH] |Betacoronavirus/*genetics/growth & development/immunology/metabolism[MESH] |COVID-19[MESH] |Coronavirus Infections/genetics/immunology/metabolism/*virology[MESH] |DNA, Mitochondrial/*genetics/metabolism[MESH] |Gene Expression Regulation, Viral[MESH] |Host Microbial Interactions[MESH] |Humans[MESH] |Immunity, Innate[MESH] |Mitochondria/*genetics/immunology/metabolism/virology[MESH] |Pandemics[MESH] |Peptidyl-Dipeptidase A/genetics/metabolism[MESH] |Pneumonia, Viral/genetics/immunology/metabolism/*virology[MESH] |RNA, Viral/*genetics[MESH] |SARS-CoV-2[MESH]Decoding SARS-CoV-2 hijacking of host mitochondria in COVID-19 pathoge(epmc).pdf DeepDyve Pubget Overpricing