Hartman Institute for Therapeutic Organ Regeneration

SARS-CoV-2 infection induces beta cell transdifferentiation.

TitleSARS-CoV-2 infection induces beta cell transdifferentiation.
Publication TypeJournal Article
Year of Publication2021
AuthorsTang X, Uhl S, Zhang T, Xue D, Li B, J Vandana J, Acklin JA, Bonnycastle LL, Narisu N, Erdos MR, Bram Y, Chandar V, Chong AChi Nok, Lacko LA, Min Z, Lim JK, Borczuk AC, Xiang J, Naji A, Collins FS, Evans T, Liu C, tenOever BR, Schwartz RE, Chen S
JournalCell Metab
Volume33
Issue8
Pagination1577-1591.e7
Date Published2021 Aug 03
ISSN1932-7420
KeywordsAcetamides, Adolescent, Adult, Aged, Aged, 80 and over, Animals, Cell Transdifferentiation, Chlorocebus aethiops, COVID-19, Cyclohexylamines, Cytokines, Eukaryotic Initiation Factor-2, Female, Glucagon, Host-Pathogen Interactions, Humans, Insulin, Insulin-Secreting Cells, Male, Middle Aged, Phenotype, SARS-CoV-2, Signal Transduction, Tissue Culture Techniques, Trypsin, Vero Cells, Young Adult
Abstract

<p>Recent clinical data have suggested a correlation between coronavirus disease 2019 (COVID-19) and diabetes. Here, we describe the detection of SARS-CoV-2 viral antigen in pancreatic beta cells in autopsy samples from individuals with COVID-19. Single-cell RNA sequencing and immunostaining from ex vivo infections confirmed that multiple types of pancreatic islet cells were susceptible to SARS-CoV-2, eliciting a cellular stress response and the induction of chemokines. Upon SARS-CoV-2 infection, beta cells showed a lower expression of insulin and a higher expression of alpha and acinar cell markers, including glucagon and trypsin1, respectively, suggesting cellular transdifferentiation. Trajectory analysis indicated that SARS-CoV-2 induced eIF2-pathway-mediated beta cell transdifferentiation, a phenotype that could be reversed with trans-integrated stress response inhibitor (trans-ISRIB). Altogether, this study demonstrates an example of SARS-CoV-2 infection causing cell fate change, which provides further insight into the pathomechanisms of COVID-19.</p>

DOI10.1016/j.cmet.2021.05.015
Alternate JournalCell Metab
PubMed ID34081913
PubMed Central IDPMC8133495
Grant ListDP3 DK111907 / DK / NIDDK NIH HHS / United States
ZIA HG000024 / ImNIH / Intramural NIH HHS / United States
R01 DK119667 / DK / NIDDK NIH HHS / United States
R01 CA234614 / CA / NCI NIH HHS / United States
R01 DK124463 / DK / NIDDK NIH HHS / United States
R03 DK117252 / DK / NIDDK NIH HHS / United States
R01 DK116075 / DK / NIDDK NIH HHS / United States
UC4 DK112217 / DK / NIDDK NIH HHS / United States
R01 AI107301 / AI / NIAID NIH HHS / United States
F32 HD096810 / HD / NICHD NIH HHS / United States
U01 DK127777 / DK / NIDDK NIH HHS / United States
P30 DK020541 / DK / NIDDK NIH HHS / United States
R01 DK121072 / DK / NIDDK NIH HHS / United States
P60 DK020541 / DK / NIDDK NIH HHS / United States

Weill Cornell Medicine
Hartman Institute for Therapeutic Organ Regeneration
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