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ACE2 and SARS-CoV-2 Expression in the Normal and COVID-19 Pancreas
Irina Kusmartseva; Wenting Wu; Farooq Syed; Verena van der Heide; Marda Jorgensen; Paul Joseph; Xiaohan Tang; Eduardo Candelario-Jalil; Changjun Yang; Harry Nick; Jack Harbert; Amanda L Posgai; Richard Lloyd; Sirlene Cechin; Alberto Pugliese; Martha Campbell-Thompson; Richard S Vander Heide; Carmella Evans-Molina; Dirk Homann; Mark A. Atkinson.
Affiliation
  • Irina Kusmartseva; University of Florida
  • Wenting Wu; Indiana University
  • Farooq Syed; Indiana University
  • Verena van der Heide; Icahn School of Medicine at Mount Sinai
  • Marda Jorgensen; University of Florida
  • Paul Joseph; University of Florida
  • Xiaohan Tang; University of Florida
  • Eduardo Candelario-Jalil; University of Florida
  • Changjun Yang; University of Florida
  • Harry Nick; University of Florida
  • Jack Harbert; Louisiana State University
  • Amanda L Posgai; University of Florida
  • Richard Lloyd; Baylor College of Medicine
  • Sirlene Cechin; University of Miami
  • Alberto Pugliese; University of Miami
  • Martha Campbell-Thompson; University of Florida
  • Richard S Vander Heide; Louisiana State University
  • Carmella Evans-Molina; Indiana University
  • Dirk Homann; Icahn School of Medicine at Mount Sinai
  • Mark A. Atkinson; University of Florida
Preprint in English | bioRxiv | ID: ppbiorxiv-270736
ABSTRACT
Diabetes is associated with increased mortality from Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2). Given literature suggesting a potential association between SARS-CoV-2 infection and diabetes induction, we examined pancreatic expression of the key molecule for SARS-CoV-2 infection of cells, angiotensin-converting enzyme-2 (ACE2). Specifically, we analyzed five public scRNAseq pancreas datasets and performed fluorescence in situ hybridization, Western blotting, and immunolocalization for ACE2 with extensive reagent validation on normal human pancreatic tissues across the lifespan, as well as those from coronavirus disease 2019 (COVID-19) patients. These in silico and ex vivo analyses demonstrated pancreatic expression of ACE2 is prominent in pancreatic ductal epithelium and the microvasculature, with rare endocrine cell expression of this molecule. Pancreata from COVID-19 patients demonstrated multiple thrombotic lesions with SARS-CoV-2 nucleocapsid protein expression primarily limited to ducts. SARS-CoV-2 infection of pancreatic endocrine cells, via ACE2, appears an unlikely central pathogenic feature of COVID-19 as it relates to diabetes.
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Full text: Available Collection: Preprints Database: bioRxiv Type of study: Prognostic study Language: English Year: 2020 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Prognostic study Language: English Year: 2020 Document type: Preprint
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