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10.1091/mbc.E21-02-0074

http://scihub22266oqcxt.onion/10.1091/mbc.E21-02-0074
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suck abstract from ncbi


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pmid34010015      Mol+Biol+Cell 2021 ; 32 (14): 1273-1282
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  • Peroxisomes exhibit compromised structure and matrix protein content in SARS-CoV-2-infected cells #MMPMID34010015
  • Knoblach B; Ishida R; Hobman TC; Rachubinski RA
  • Mol Biol Cell 2021[Jul]; 32 (14): 1273-1282 PMID34010015show ga
  • Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel coronavirus that has triggered global health and economic crises. Here we report the effects of SARS-CoV-2 infection on peroxisomes of human cell lines Huh-7 and SK-N-SH. Peroxisomes undergo dramatic changes in morphology in SARS-CoV-2-infected cells. Rearrangement of peroxisomal membranes is followed by redistribution of peroxisomal matrix proteins to the cytosol, resulting in a dramatic decrease in the number of mature peroxisomes. The SARS-CoV-2 ORF14 protein was shown to interact physically with human PEX14, a peroxisomal membrane protein required for matrix protein import and peroxisome biogenesis. Given the important roles of peroxisomes in innate immunity, SARS-CoV-2 may directly target peroxisomes, resulting in loss of peroxisome structural integrity, matrix protein content and ability to function in antiviral signaling.
  • |Animals[MESH]
  • |Cell Line[MESH]
  • |Cell Membrane/pathology[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Coronavirus Nucleocapsid Proteins/metabolism[MESH]
  • |Extracellular Matrix Proteins/metabolism[MESH]
  • |Humans[MESH]
  • |Membrane Proteins/metabolism[MESH]
  • |Peroxisomes/metabolism/pathology/*virology[MESH]
  • |Phosphoproteins/metabolism[MESH]
  • |Repressor Proteins/metabolism[MESH]
  • |SARS-CoV-2/metabolism[MESH]


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