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10.1016/j.isci.2020.101611

http://scihub22266oqcxt.onion/10.1016/j.isci.2020.101611
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33015591!7518203!33015591
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suck abstract from ncbi


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pmid33015591      iScience 2020 ; 23 (10): 101611
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  • PPARgamma Cistrome Repression during Activation of Lung Monocyte-Macrophages in Severe COVID-19 #MMPMID33015591
  • Desterke C; Turhan AG; Bennaceur-Griscelli A; Griscelli F
  • iScience 2020[Oct]; 23 (10): 101611 PMID33015591show ga
  • The molecular mechanisms of cytokine storm in patients with severe COVID-19 infections are poorly understood. To uncover these events, we performed transcriptome analyses of lung biopsies from patients with COVID-19, revealing a gene enrichment pattern similar to that of PPARgamma-knockout macrophages. Single-cell gene expression analysis of bronchoalveolar lavage fluids revealed a characteristic trajectory of PPARgamma-related disturbance in the CD14+/CD16+ cells. We identified a correlation with the disease severity and the reduced expression of several members of the PPARgamma complex such as EP300, RXRA, RARA, SUMO1, NR3C1, and CCDC88A. ChIP-seq analyses confirmed repression of the PPARgamma-RXRA-NR3C1 cistrome in COVID-19 lung samples. Further analysis of protein-protein networks highlighted an interaction between the PPARgamma-associated protein SUMO1 and a nucleoprotein of the SARS virus. Overall, these results demonstrate for the first time the involvement of the PPARgamma complex in severe COVID-19 lung disease and suggest strongly its role in the major monocyte/macrophage-mediated inflammatory storm.
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