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Stress Decreases Host Viral Resistance and Increases Covid Susceptibility in Embryonic Stem Cells
Stress-induced changes in viral receptor and susceptibility gene expression were measured in embryonic stem cells (ESC) and differentiated progeny. Rex1 promoter-Red Fluorescence Protein reporter ESC were tested by RNAseq after 72hr exposures to control stress hyperosmotic sorbitol under stemness cu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216586/ https://www.ncbi.nlm.nih.gov/pubmed/34155611 http://dx.doi.org/10.1007/s12015-021-10188-w |
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author | Abdulhasan, Mohammed Ruden, Ximena Rappolee, Benjamin Dutta, Sudipta Gurdziel, Katherine Ruden, Douglas M. Awonuga, Awoniyi O Korzeniewski, Steve J. Puscheck, Elizabeth E. Rappolee, Daniel A. |
author_facet | Abdulhasan, Mohammed Ruden, Ximena Rappolee, Benjamin Dutta, Sudipta Gurdziel, Katherine Ruden, Douglas M. Awonuga, Awoniyi O Korzeniewski, Steve J. Puscheck, Elizabeth E. Rappolee, Daniel A. |
author_sort | Abdulhasan, Mohammed |
collection | PubMed |
description | Stress-induced changes in viral receptor and susceptibility gene expression were measured in embryonic stem cells (ESC) and differentiated progeny. Rex1 promoter-Red Fluorescence Protein reporter ESC were tested by RNAseq after 72hr exposures to control stress hyperosmotic sorbitol under stemness culture (NS) to quantify stress-forced differentiation (SFD) transcriptomic programs. Control ESC cultured with stemness factor removal produced normal differentiation (ND). Bulk RNAseq transcriptomic analysis showed significant upregulation of two genes involved in Covid-19 cell uptake, Vimentin (VIM) and Transmembrane Serine Protease 2 (TMPRSS2). SFD increased the hepatitis A virus receptor (Havcr1) and the transplacental Herpes simplex 1 (HSV1) virus receptor (Pvrl1) compared with ESC undergoing ND. Several other coronavirus receptors, Glutamyl Aminopeptidase (ENPEP) and Dipeptidyl Peptidase 4 (DPP4) were upregulated significantly in SFD>ND. Although stressed ESC are more susceptible to infection due to increased expression of viral receptors and decreased resistance, the necessary Covid-19 receptor, angiotensin converting enzyme (ACE)2, was not expressed in our experiments. TMPRSS2, ENPEP, and DPP4 mediate Coronavirus uptake, but are also markers of extra-embryonic endoderm (XEN), which arise from ESC undergoing ND or SFD. Mouse and human ESCs differentiated to XEN increase TMPRSS2 and other Covid-19 uptake-mediating gene expression, but only some lines express ACE2. Covid-19 susceptibility appears to be genotype-specific and not ubiquitous. Of the 30 gene ontology (GO) groups for viral susceptibility, 15 underwent significant stress-forced changes. Of these, 4 GO groups mediated negative viral regulation and most genes in these increase in ND and decrease with SFD, thus suggesting that stress increases ESC viral susceptibility. Taken together, the data suggest that a control hyperosmotic stress can increase Covid-19 susceptibility and decrease viral host resistance in mouse ESC. However, this limited pilot study should be followed with studies in human ESC, tests of environmental, hormonal, and pharmaceutical stressors and direct tests for infection of stressed, cultured ESC and embryos by Covid-19. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12015-021-10188-w. |
format | Online Article Text |
id | pubmed-8216586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-82165862021-06-23 Stress Decreases Host Viral Resistance and Increases Covid Susceptibility in Embryonic Stem Cells Abdulhasan, Mohammed Ruden, Ximena Rappolee, Benjamin Dutta, Sudipta Gurdziel, Katherine Ruden, Douglas M. Awonuga, Awoniyi O Korzeniewski, Steve J. Puscheck, Elizabeth E. Rappolee, Daniel A. Stem Cell Rev Rep Article Stress-induced changes in viral receptor and susceptibility gene expression were measured in embryonic stem cells (ESC) and differentiated progeny. Rex1 promoter-Red Fluorescence Protein reporter ESC were tested by RNAseq after 72hr exposures to control stress hyperosmotic sorbitol under stemness culture (NS) to quantify stress-forced differentiation (SFD) transcriptomic programs. Control ESC cultured with stemness factor removal produced normal differentiation (ND). Bulk RNAseq transcriptomic analysis showed significant upregulation of two genes involved in Covid-19 cell uptake, Vimentin (VIM) and Transmembrane Serine Protease 2 (TMPRSS2). SFD increased the hepatitis A virus receptor (Havcr1) and the transplacental Herpes simplex 1 (HSV1) virus receptor (Pvrl1) compared with ESC undergoing ND. Several other coronavirus receptors, Glutamyl Aminopeptidase (ENPEP) and Dipeptidyl Peptidase 4 (DPP4) were upregulated significantly in SFD>ND. Although stressed ESC are more susceptible to infection due to increased expression of viral receptors and decreased resistance, the necessary Covid-19 receptor, angiotensin converting enzyme (ACE)2, was not expressed in our experiments. TMPRSS2, ENPEP, and DPP4 mediate Coronavirus uptake, but are also markers of extra-embryonic endoderm (XEN), which arise from ESC undergoing ND or SFD. Mouse and human ESCs differentiated to XEN increase TMPRSS2 and other Covid-19 uptake-mediating gene expression, but only some lines express ACE2. Covid-19 susceptibility appears to be genotype-specific and not ubiquitous. Of the 30 gene ontology (GO) groups for viral susceptibility, 15 underwent significant stress-forced changes. Of these, 4 GO groups mediated negative viral regulation and most genes in these increase in ND and decrease with SFD, thus suggesting that stress increases ESC viral susceptibility. Taken together, the data suggest that a control hyperosmotic stress can increase Covid-19 susceptibility and decrease viral host resistance in mouse ESC. However, this limited pilot study should be followed with studies in human ESC, tests of environmental, hormonal, and pharmaceutical stressors and direct tests for infection of stressed, cultured ESC and embryos by Covid-19. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12015-021-10188-w. Springer US 2021-06-21 2021 /pmc/articles/PMC8216586/ /pubmed/34155611 http://dx.doi.org/10.1007/s12015-021-10188-w Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Abdulhasan, Mohammed Ruden, Ximena Rappolee, Benjamin Dutta, Sudipta Gurdziel, Katherine Ruden, Douglas M. Awonuga, Awoniyi O Korzeniewski, Steve J. Puscheck, Elizabeth E. Rappolee, Daniel A. Stress Decreases Host Viral Resistance and Increases Covid Susceptibility in Embryonic Stem Cells |
title | Stress Decreases Host Viral Resistance and Increases Covid Susceptibility in Embryonic Stem Cells |
title_full | Stress Decreases Host Viral Resistance and Increases Covid Susceptibility in Embryonic Stem Cells |
title_fullStr | Stress Decreases Host Viral Resistance and Increases Covid Susceptibility in Embryonic Stem Cells |
title_full_unstemmed | Stress Decreases Host Viral Resistance and Increases Covid Susceptibility in Embryonic Stem Cells |
title_short | Stress Decreases Host Viral Resistance and Increases Covid Susceptibility in Embryonic Stem Cells |
title_sort | stress decreases host viral resistance and increases covid susceptibility in embryonic stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216586/ https://www.ncbi.nlm.nih.gov/pubmed/34155611 http://dx.doi.org/10.1007/s12015-021-10188-w |
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