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10.1080/19382014.2021.1954458

http://scihub22266oqcxt.onion/10.1080/19382014.2021.1954458
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34304698!8528404!34304698
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suck abstract from ncbi


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pmid34304698      Islets 2021 ; 13 (5-6): 106-114
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  • Expression of SARS-CoV-2 receptor "ACE2" in human pancreatic beta cells: to be or not to be! #MMPMID34304698
  • El-Huneidi W; Hamad M; Taneera J
  • Islets 2021[Sep]; 13 (5-6): 106-114 PMID34304698show ga
  • The current COVID-19 pandemic, which continues to spread across the globe, is caused by severe acute respiratory syndrome coronavirus (SARS-Cov-2). Soon after the pandemic emerged in China, it became clear that the receptor-binding domain (RBD) of angiotensin-converting enzyme 2 (ACE2) serves as the primary cell surface receptor for SARS-Cov-2. Subsequent work has shown that diabetes and hyperglycemia are major risk factors for morbidity and mortality in COVID-19 patients. However, data on the pattern of expression of ACE2 on human pancreatic beta cells remain contradictory. Additionally, there is no consensus on whether the virus can directly infect and damage pancreatic islets and hence exacerbate diabetes. In this mini-review, we highlight the role of ACE2 receptor and summarize the current state of knowledge regarding its expression/co-localization in human pancreatic endocrine cells. We also discuss recent data on the permissiveness of human pancreatic beta cells to SARS-Cov-2 infection.
  • |*COVID-19[MESH]
  • |*Insulin-Secreting Cells[MESH]
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]


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