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IL-22 regulates endometrial regeneration by enhancing tight junctions and orchestrating extracellular matrix

The uterine endometrium uniquely regenerates after menses, postpartum, or after breaks in the uterine layer integrity throughout women’s lives. Direct cell–cell contacts ensured by tight and adherens junctions play an important role in endometrial integrity. Any changes in these junctions can alter...

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Autores principales: Ganieva, Umida, Schneiderman, Sylvia, Bu, Pengli, Beaman, Kenneth, Dambaeva, Svetlana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453595/
https://www.ncbi.nlm.nih.gov/pubmed/36091010
http://dx.doi.org/10.3389/fimmu.2022.955576
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author Ganieva, Umida
Schneiderman, Sylvia
Bu, Pengli
Beaman, Kenneth
Dambaeva, Svetlana
author_facet Ganieva, Umida
Schneiderman, Sylvia
Bu, Pengli
Beaman, Kenneth
Dambaeva, Svetlana
author_sort Ganieva, Umida
collection PubMed
description The uterine endometrium uniquely regenerates after menses, postpartum, or after breaks in the uterine layer integrity throughout women’s lives. Direct cell–cell contacts ensured by tight and adherens junctions play an important role in endometrial integrity. Any changes in these junctions can alter the endometrial permeability of the uterus and have an impact on the regeneration of uterine layers. Interleukin 22 (IL-22) is a cytokine that is recognized for its role in epithelial regeneration. Moreover, it is crucial in controlling the inflammatory response in mucosal tissues. Here, we studied the role of IL-22 in endometrial recovery after inflammation-triggered abortion. Fecundity of mice was studied in consecutive matings of the same animals after lipopolysaccharide (LPS) (10 µg per mouse)-triggered abortion. The fecundity rate after the second mating was substantially different between IL-22 knockout (IL-22(−/−)) (9.1%) and wild-type (WT) (71.4%) mice (p < 0.05), while there was no difference between the groups in the initial mating, suggesting that IL-22 deficiency might be associated with secondary infertility. A considerable difference was observed between IL-22(−/−) and WT mice in the uterine clearance following LPS-triggered abortion. Gross examination of the uteri of IL-22(−/−) mice revealed non-viable fetuses retained inside the horns (delayed clearance). In contrast, all WT mice had completed abortion with total clearance after LPS exposure. We also discovered that IL-22 deficiency is associated with a decreased expression of tight junctions (claudin-2 and claudin-10) and cell surface pathogen protectors (mucin-1). Moreover, IL-22 has a role in the remodeling of the uterine tissue in the inflammatory environment by regulating epithelial–mesenchymal transition markers called E- and N-cadherin. Therefore, IL-22 contributes to the proper regeneration of endometrial layers after inflammation-triggered abortion. Thus, it might have a practical significance to be utilized as a treatment option postpartum (enhanced regeneration function) and in secondary infertility caused by inflammation (enhanced barrier/protector function).
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spelling pubmed-94535952022-09-09 IL-22 regulates endometrial regeneration by enhancing tight junctions and orchestrating extracellular matrix Ganieva, Umida Schneiderman, Sylvia Bu, Pengli Beaman, Kenneth Dambaeva, Svetlana Front Immunol Immunology The uterine endometrium uniquely regenerates after menses, postpartum, or after breaks in the uterine layer integrity throughout women’s lives. Direct cell–cell contacts ensured by tight and adherens junctions play an important role in endometrial integrity. Any changes in these junctions can alter the endometrial permeability of the uterus and have an impact on the regeneration of uterine layers. Interleukin 22 (IL-22) is a cytokine that is recognized for its role in epithelial regeneration. Moreover, it is crucial in controlling the inflammatory response in mucosal tissues. Here, we studied the role of IL-22 in endometrial recovery after inflammation-triggered abortion. Fecundity of mice was studied in consecutive matings of the same animals after lipopolysaccharide (LPS) (10 µg per mouse)-triggered abortion. The fecundity rate after the second mating was substantially different between IL-22 knockout (IL-22(−/−)) (9.1%) and wild-type (WT) (71.4%) mice (p < 0.05), while there was no difference between the groups in the initial mating, suggesting that IL-22 deficiency might be associated with secondary infertility. A considerable difference was observed between IL-22(−/−) and WT mice in the uterine clearance following LPS-triggered abortion. Gross examination of the uteri of IL-22(−/−) mice revealed non-viable fetuses retained inside the horns (delayed clearance). In contrast, all WT mice had completed abortion with total clearance after LPS exposure. We also discovered that IL-22 deficiency is associated with a decreased expression of tight junctions (claudin-2 and claudin-10) and cell surface pathogen protectors (mucin-1). Moreover, IL-22 has a role in the remodeling of the uterine tissue in the inflammatory environment by regulating epithelial–mesenchymal transition markers called E- and N-cadherin. Therefore, IL-22 contributes to the proper regeneration of endometrial layers after inflammation-triggered abortion. Thus, it might have a practical significance to be utilized as a treatment option postpartum (enhanced regeneration function) and in secondary infertility caused by inflammation (enhanced barrier/protector function). Frontiers Media S.A. 2022-08-25 /pmc/articles/PMC9453595/ /pubmed/36091010 http://dx.doi.org/10.3389/fimmu.2022.955576 Text en Copyright © 2022 Ganieva, Schneiderman, Bu, Beaman and Dambaeva https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Ganieva, Umida
Schneiderman, Sylvia
Bu, Pengli
Beaman, Kenneth
Dambaeva, Svetlana
IL-22 regulates endometrial regeneration by enhancing tight junctions and orchestrating extracellular matrix
title IL-22 regulates endometrial regeneration by enhancing tight junctions and orchestrating extracellular matrix
title_full IL-22 regulates endometrial regeneration by enhancing tight junctions and orchestrating extracellular matrix
title_fullStr IL-22 regulates endometrial regeneration by enhancing tight junctions and orchestrating extracellular matrix
title_full_unstemmed IL-22 regulates endometrial regeneration by enhancing tight junctions and orchestrating extracellular matrix
title_short IL-22 regulates endometrial regeneration by enhancing tight junctions and orchestrating extracellular matrix
title_sort il-22 regulates endometrial regeneration by enhancing tight junctions and orchestrating extracellular matrix
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453595/
https://www.ncbi.nlm.nih.gov/pubmed/36091010
http://dx.doi.org/10.3389/fimmu.2022.955576
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