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Plasma membrane receptor mediated MAPK signaling pathways are activated in human uterine cervix at parturition
BACKGROUND: Cervical ripening resembles an inflammatory reaction. Estrogens induce leukocyte migration into tissue and factors promoting cervical remodeling and labor, although the mechanisms are only partially known. The aim of this study was to investigate whether plasma membrane receptor mediated...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1796879/ https://www.ncbi.nlm.nih.gov/pubmed/17257441 http://dx.doi.org/10.1186/1477-7827-5-3 |
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author | Wang, Hong Stjernholm, Ylva Vladic |
author_facet | Wang, Hong Stjernholm, Ylva Vladic |
author_sort | Wang, Hong |
collection | PubMed |
description | BACKGROUND: Cervical ripening resembles an inflammatory reaction. Estrogens induce leukocyte migration into tissue and factors promoting cervical remodeling and labor, although the mechanisms are only partially known. The aim of this study was to investigate whether plasma membrane receptor mediated pathways, known to be activated by estrogens and proinflammatory compounds, are involved in cervical ripening before labor. METHODS: The expression and distribution of mitogen activated protein kinases (MAPK), which transduce extracellular signals into intracellular responses through phosphorylation, and their intracellular targets transcription factors c-Jun and c-Fos proteins (AP-1) were analysed in cervical biopsies from term pregnant women (TP), immediately after parturition (PP), and from non-pregnant women (NP). Immunohistochemistry and RT-PCR techniques were used. RESULTS: Cell-specific alterations in the immunostaining pattern for MAPK were observed. The expressions of activated, phosphorylated MAPK forms pERK1/2, pJNK and p38MAPK were significantly increased in cervical stroma until TP and pERK1/2 expression was significantly enhanced in PP group. c-Jun was significantly increased in cervical stroma and smooth muscle in TP as compared to NP group. c-Fos was significantly increased in stroma, squamous epithelium and glandular epithelium in PP as compared to TP group. CONCLUSION: We report, for the first time, cell-specific activation of pMAPKs and their targets transcription factors c-Fos and c-Jun (AP-1) proteins in human uterine cervix until term pregnancy, and immediately after parturition. These results suggest a role for MAPK activation in cervical ripening before labor. |
format | Text |
id | pubmed-1796879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-17968792007-02-10 Plasma membrane receptor mediated MAPK signaling pathways are activated in human uterine cervix at parturition Wang, Hong Stjernholm, Ylva Vladic Reprod Biol Endocrinol Research BACKGROUND: Cervical ripening resembles an inflammatory reaction. Estrogens induce leukocyte migration into tissue and factors promoting cervical remodeling and labor, although the mechanisms are only partially known. The aim of this study was to investigate whether plasma membrane receptor mediated pathways, known to be activated by estrogens and proinflammatory compounds, are involved in cervical ripening before labor. METHODS: The expression and distribution of mitogen activated protein kinases (MAPK), which transduce extracellular signals into intracellular responses through phosphorylation, and their intracellular targets transcription factors c-Jun and c-Fos proteins (AP-1) were analysed in cervical biopsies from term pregnant women (TP), immediately after parturition (PP), and from non-pregnant women (NP). Immunohistochemistry and RT-PCR techniques were used. RESULTS: Cell-specific alterations in the immunostaining pattern for MAPK were observed. The expressions of activated, phosphorylated MAPK forms pERK1/2, pJNK and p38MAPK were significantly increased in cervical stroma until TP and pERK1/2 expression was significantly enhanced in PP group. c-Jun was significantly increased in cervical stroma and smooth muscle in TP as compared to NP group. c-Fos was significantly increased in stroma, squamous epithelium and glandular epithelium in PP as compared to TP group. CONCLUSION: We report, for the first time, cell-specific activation of pMAPKs and their targets transcription factors c-Fos and c-Jun (AP-1) proteins in human uterine cervix until term pregnancy, and immediately after parturition. These results suggest a role for MAPK activation in cervical ripening before labor. BioMed Central 2007-01-28 /pmc/articles/PMC1796879/ /pubmed/17257441 http://dx.doi.org/10.1186/1477-7827-5-3 Text en Copyright © 2007 Wang and Stjernholm; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Wang, Hong Stjernholm, Ylva Vladic Plasma membrane receptor mediated MAPK signaling pathways are activated in human uterine cervix at parturition |
title | Plasma membrane receptor mediated MAPK signaling pathways are activated in human uterine cervix at parturition |
title_full | Plasma membrane receptor mediated MAPK signaling pathways are activated in human uterine cervix at parturition |
title_fullStr | Plasma membrane receptor mediated MAPK signaling pathways are activated in human uterine cervix at parturition |
title_full_unstemmed | Plasma membrane receptor mediated MAPK signaling pathways are activated in human uterine cervix at parturition |
title_short | Plasma membrane receptor mediated MAPK signaling pathways are activated in human uterine cervix at parturition |
title_sort | plasma membrane receptor mediated mapk signaling pathways are activated in human uterine cervix at parturition |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1796879/ https://www.ncbi.nlm.nih.gov/pubmed/17257441 http://dx.doi.org/10.1186/1477-7827-5-3 |
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