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Heterogeneous Escape from X Chromosome Inactivation Results in Sex Differences in Type I IFN Responses at the Single Human pDC Level
Immune responses differ between women and men, and type I interferon (IFN) responses following Toll-like receptor 7 (TLR7) stimulation are higher in women. The precise mechanisms driving these sex differences in immunity are unknown. To investigate possible genetic factors, we quantify escape from X...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7833293/ https://www.ncbi.nlm.nih.gov/pubmed/33296655 http://dx.doi.org/10.1016/j.celrep.2020.108485 |
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author | Hagen, Sven Hendrik Henseling, Florian Hennesen, Jana Savel, Hélène Delahaye, Solenne Richert, Laura Ziegler, Susanne Maria Altfeld, Marcus |
author_facet | Hagen, Sven Hendrik Henseling, Florian Hennesen, Jana Savel, Hélène Delahaye, Solenne Richert, Laura Ziegler, Susanne Maria Altfeld, Marcus |
author_sort | Hagen, Sven Hendrik |
collection | PubMed |
description | Immune responses differ between women and men, and type I interferon (IFN) responses following Toll-like receptor 7 (TLR7) stimulation are higher in women. The precise mechanisms driving these sex differences in immunity are unknown. To investigate possible genetic factors, we quantify escape from X chromosome inactivation (XCI) for TLR7 and four other genes (RPS6KA3, CYBB, BTK, and IL13RA1) at the single plasmacytoid dendritic cell (pDC) level. We observe escape from XCI for all investigated genes, leading to biallelic expression patterns. pDCs with biallelic gene expression have significantly higher mRNA levels of the respective genes. Unstimulated pDCs with biallelic TLR7 expression exhibit significantly higher IFNα/β mRNA levels, and IFNα exposure results in significantly increased IFNα/β protein production by pDCs. These results identify unanticipated heterogeneity in escape from XCI of several genes in pDCs and highlight the important contribution of X chromosome factors to sex differences in type I IFN responses, which might explain observed sex differences in human diseases. |
format | Online Article Text |
id | pubmed-7833293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Authors. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78332932021-01-26 Heterogeneous Escape from X Chromosome Inactivation Results in Sex Differences in Type I IFN Responses at the Single Human pDC Level Hagen, Sven Hendrik Henseling, Florian Hennesen, Jana Savel, Hélène Delahaye, Solenne Richert, Laura Ziegler, Susanne Maria Altfeld, Marcus Cell Rep Report Immune responses differ between women and men, and type I interferon (IFN) responses following Toll-like receptor 7 (TLR7) stimulation are higher in women. The precise mechanisms driving these sex differences in immunity are unknown. To investigate possible genetic factors, we quantify escape from X chromosome inactivation (XCI) for TLR7 and four other genes (RPS6KA3, CYBB, BTK, and IL13RA1) at the single plasmacytoid dendritic cell (pDC) level. We observe escape from XCI for all investigated genes, leading to biallelic expression patterns. pDCs with biallelic gene expression have significantly higher mRNA levels of the respective genes. Unstimulated pDCs with biallelic TLR7 expression exhibit significantly higher IFNα/β mRNA levels, and IFNα exposure results in significantly increased IFNα/β protein production by pDCs. These results identify unanticipated heterogeneity in escape from XCI of several genes in pDCs and highlight the important contribution of X chromosome factors to sex differences in type I IFN responses, which might explain observed sex differences in human diseases. The Authors. 2020-12-08 2020-12-08 /pmc/articles/PMC7833293/ /pubmed/33296655 http://dx.doi.org/10.1016/j.celrep.2020.108485 Text en © 2020 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Report Hagen, Sven Hendrik Henseling, Florian Hennesen, Jana Savel, Hélène Delahaye, Solenne Richert, Laura Ziegler, Susanne Maria Altfeld, Marcus Heterogeneous Escape from X Chromosome Inactivation Results in Sex Differences in Type I IFN Responses at the Single Human pDC Level |
title | Heterogeneous Escape from X Chromosome Inactivation Results in Sex Differences in Type I IFN Responses at the Single Human pDC Level |
title_full | Heterogeneous Escape from X Chromosome Inactivation Results in Sex Differences in Type I IFN Responses at the Single Human pDC Level |
title_fullStr | Heterogeneous Escape from X Chromosome Inactivation Results in Sex Differences in Type I IFN Responses at the Single Human pDC Level |
title_full_unstemmed | Heterogeneous Escape from X Chromosome Inactivation Results in Sex Differences in Type I IFN Responses at the Single Human pDC Level |
title_short | Heterogeneous Escape from X Chromosome Inactivation Results in Sex Differences in Type I IFN Responses at the Single Human pDC Level |
title_sort | heterogeneous escape from x chromosome inactivation results in sex differences in type i ifn responses at the single human pdc level |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7833293/ https://www.ncbi.nlm.nih.gov/pubmed/33296655 http://dx.doi.org/10.1016/j.celrep.2020.108485 |
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