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suck abstract from ncbi


10.1016/j.stemcr.2021.02.001

http://scihub22266oqcxt.onion/10.1016/j.stemcr.2021.02.001
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33581053!7862909!33581053
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suck abstract from ncbi

pmid33581053      Stem+Cell+Reports 2021 ; 16 (3): 428-436
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  • Human Erythroid Progenitors Are Directly Infected by SARS-CoV-2: Implications for Emerging Erythropoiesis in Severe COVID-19 Patients #MMPMID33581053
  • Huerga Encabo H; Grey W; Garcia-Albornoz M; Wood H; Ulferts R; Aramburu IV; Kulasekararaj AG; Mufti G; Papayannopoulos V; Beale R; Bonnet D
  • Stem Cell Reports 2021[Mar]; 16 (3): 428-436 PMID33581053show ga
  • We document here that intensive care COVID-19 patients suffer a profound decline in hemoglobin levels but show an increase of circulating nucleated red cells, suggesting that SARS-CoV-2 infection either directly or indirectly induces stress erythropoiesis. We show that ACE2 expression peaks during erythropoiesis and renders erythroid progenitors vulnerable to infection by SARS-CoV-2. Early erythroid progenitors, defined as CD34(-)CD117(+)CD71(+)CD235a(-), show the highest levels of ACE2 and constitute the primary target cell to be infected during erythropoiesis. SARS-CoV-2 causes the expansion of colony formation by erythroid progenitors and can be detected in these cells after 2 weeks of the initial infection. Our findings constitute the first report of SARS-CoV-2 infectivity in erythroid progenitor cells and can contribute to understanding both the clinical symptoms of severe COVID-19 patients and how the virus can spread through the circulation to produce local inflammation in tissues, including the bone marrow.
  • |Angiotensin-Converting Enzyme 2/metabolism[MESH]
  • |Animals[MESH]
  • |COVID-19/metabolism/*virology[MESH]
  • |Cell Line[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Erythroid Precursor Cells/metabolism/*virology[MESH]
  • |Erythropoiesis/*physiology[MESH]
  • |Humans[MESH]
  • |Inflammation/metabolism/virology[MESH]
  • |SARS-CoV-2/*pathogenicity[MESH]


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