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Myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice

This study aimed to determine the mechanism of uterine activation during labour, both term (TL) and preterm (PTL). We hypothesized that the peripheral leucocytes are recruited to uterine tissues by locally produced cytokines where they contribute to the initiation of parturition. Mouse uteri were co...

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Autores principales: Shynlova, Oksana, Nedd-Roderique, Tamara, Li, Yunqing, Dorogin, Anna, Lye, Stephen J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823139/
https://www.ncbi.nlm.nih.gov/pubmed/23205502
http://dx.doi.org/10.1111/j.1582-4934.2012.01650.x
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author Shynlova, Oksana
Nedd-Roderique, Tamara
Li, Yunqing
Dorogin, Anna
Lye, Stephen J
author_facet Shynlova, Oksana
Nedd-Roderique, Tamara
Li, Yunqing
Dorogin, Anna
Lye, Stephen J
author_sort Shynlova, Oksana
collection PubMed
description This study aimed to determine the mechanism of uterine activation during labour, both term (TL) and preterm (PTL). We hypothesized that the peripheral leucocytes are recruited to uterine tissues by locally produced cytokines where they contribute to the initiation of parturition. Mouse uteri were collected (i) during gestation, TL and post-partum (PP), (ii) during PTL initiated by intrauterine infusion of LPS (125 μg) or (iii) injection of the progesterone receptor antagonist RU486 and analysed for multiple cytokine expression levels by real-time polymerase chain reaction (RT-PCR) and 23-plex Cytokine assay or enzymatically dispersed for assessment of immune cell populations. Markers of myeloid cell differentiation (Gr1, Neu7/4 and F4/80) were evaluated by FACS to define tissue macrophages (Macs), monocytes (M) and neutrophils (N) and by immunohistochemistry to detect tissue Macs and N. Our results indicate that: (1) Macs were elevated in mouse myometrium before TL (P < 0.05) followed by an increase in M and N; these changes were accompanied by an increase in multiple pro-inflammatory cytokines/chemokines genes. The expression of corresponding proteins increased PP. (2) TL and RU486-PTL models showed similar gene/protein expression profiles, (3) LPS-PTL was characterized by strong pro-inflammatory response and massive influx of N in myometrial tissues showing a pattern different from TL and RU486-PTL, (4) The PP period appears similar in all three models, with elevated myometrial cytokine levels and high infiltration of immune cells. We concluded that leucocytes infiltrate myometrium around the time of parturition implicating their potential role in labour activation (both term and preterm) and major role in PP uterine involution.
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spelling pubmed-38231392014-12-03 Myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice Shynlova, Oksana Nedd-Roderique, Tamara Li, Yunqing Dorogin, Anna Lye, Stephen J J Cell Mol Med Original Articles This study aimed to determine the mechanism of uterine activation during labour, both term (TL) and preterm (PTL). We hypothesized that the peripheral leucocytes are recruited to uterine tissues by locally produced cytokines where they contribute to the initiation of parturition. Mouse uteri were collected (i) during gestation, TL and post-partum (PP), (ii) during PTL initiated by intrauterine infusion of LPS (125 μg) or (iii) injection of the progesterone receptor antagonist RU486 and analysed for multiple cytokine expression levels by real-time polymerase chain reaction (RT-PCR) and 23-plex Cytokine assay or enzymatically dispersed for assessment of immune cell populations. Markers of myeloid cell differentiation (Gr1, Neu7/4 and F4/80) were evaluated by FACS to define tissue macrophages (Macs), monocytes (M) and neutrophils (N) and by immunohistochemistry to detect tissue Macs and N. Our results indicate that: (1) Macs were elevated in mouse myometrium before TL (P < 0.05) followed by an increase in M and N; these changes were accompanied by an increase in multiple pro-inflammatory cytokines/chemokines genes. The expression of corresponding proteins increased PP. (2) TL and RU486-PTL models showed similar gene/protein expression profiles, (3) LPS-PTL was characterized by strong pro-inflammatory response and massive influx of N in myometrial tissues showing a pattern different from TL and RU486-PTL, (4) The PP period appears similar in all three models, with elevated myometrial cytokine levels and high infiltration of immune cells. We concluded that leucocytes infiltrate myometrium around the time of parturition implicating their potential role in labour activation (both term and preterm) and major role in PP uterine involution. Blackwell Publishing Ltd 2013-01 2012-12-04 /pmc/articles/PMC3823139/ /pubmed/23205502 http://dx.doi.org/10.1111/j.1582-4934.2012.01650.x Text en Copyright © 2013 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Articles
Shynlova, Oksana
Nedd-Roderique, Tamara
Li, Yunqing
Dorogin, Anna
Lye, Stephen J
Myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice
title Myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice
title_full Myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice
title_fullStr Myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice
title_full_unstemmed Myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice
title_short Myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice
title_sort myometrial immune cells contribute to term parturition, preterm labour and post-partum involution in mice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823139/
https://www.ncbi.nlm.nih.gov/pubmed/23205502
http://dx.doi.org/10.1111/j.1582-4934.2012.01650.x
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