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High stretch cycling inhibits the morphological and biological decidual process in human endometrial stromal cells
PURPOSE: Subendometrial myometrium exerts wave‐like activity throughout the menstrual cycle, and uterine peristalsis is markedly reduced during the implantation phase. We hypothesized that abnormal uterine peristalsis has an adverse effect on the endometrial decidualization process. We conducted an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542020/ https://www.ncbi.nlm.nih.gov/pubmed/33071640 http://dx.doi.org/10.1002/rmb2.12341 |
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author | Saito, Ryohei Kajihara, Takeshi Takamura, Masashi Tochigi, Hideno Sato, Tsuyoshi Ishihara, Osamu |
author_facet | Saito, Ryohei Kajihara, Takeshi Takamura, Masashi Tochigi, Hideno Sato, Tsuyoshi Ishihara, Osamu |
author_sort | Saito, Ryohei |
collection | PubMed |
description | PURPOSE: Subendometrial myometrium exerts wave‐like activity throughout the menstrual cycle, and uterine peristalsis is markedly reduced during the implantation phase. We hypothesized that abnormal uterine peristalsis has an adverse effect on the endometrial decidualization process. We conducted an in vitro culture experiment to investigate the effect of cyclic stretch on the morphological and biological endometrial decidual process. METHODS: Primary human endometrial stromal cells (HESCs) were isolated from hysterectomy specimens and incubated with or without 8‐bromo‐cyclic adenosine monophosphate (8‐br‐cAMP) and medroxyprogesterone acetate (MPA) for 3 days. After decidualization, cultures were continued for 24 hours with or without cyclic stretch using a computer‐operated cell tension system. RESULTS: Cyclic stretch significantly repressed expression of decidual markers including insulin‐like growth factor‐binding protein 1 (IGFBP1), prolactin (PRL), forkhead box O1 (FOXO1), and WNT4 on decidualized HESCs. In addition, cyclic stretch of decidualized HESCs affected the decidual morphological phenotype to an elongated shape. The alternation of F‐actin localization in decidualized HESCs was not observed in response to cyclic stretch. CONCLUSIONS: These data suggest that cyclic stretch inhibits the morphological and biological decidual process of HESCs. Our findings imply that uterine abnormal contractions during the implantation period impair endometrial decidualization and contribute to infertility. |
format | Online Article Text |
id | pubmed-7542020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75420202020-10-16 High stretch cycling inhibits the morphological and biological decidual process in human endometrial stromal cells Saito, Ryohei Kajihara, Takeshi Takamura, Masashi Tochigi, Hideno Sato, Tsuyoshi Ishihara, Osamu Reprod Med Biol Original Articles PURPOSE: Subendometrial myometrium exerts wave‐like activity throughout the menstrual cycle, and uterine peristalsis is markedly reduced during the implantation phase. We hypothesized that abnormal uterine peristalsis has an adverse effect on the endometrial decidualization process. We conducted an in vitro culture experiment to investigate the effect of cyclic stretch on the morphological and biological endometrial decidual process. METHODS: Primary human endometrial stromal cells (HESCs) were isolated from hysterectomy specimens and incubated with or without 8‐bromo‐cyclic adenosine monophosphate (8‐br‐cAMP) and medroxyprogesterone acetate (MPA) for 3 days. After decidualization, cultures were continued for 24 hours with or without cyclic stretch using a computer‐operated cell tension system. RESULTS: Cyclic stretch significantly repressed expression of decidual markers including insulin‐like growth factor‐binding protein 1 (IGFBP1), prolactin (PRL), forkhead box O1 (FOXO1), and WNT4 on decidualized HESCs. In addition, cyclic stretch of decidualized HESCs affected the decidual morphological phenotype to an elongated shape. The alternation of F‐actin localization in decidualized HESCs was not observed in response to cyclic stretch. CONCLUSIONS: These data suggest that cyclic stretch inhibits the morphological and biological decidual process of HESCs. Our findings imply that uterine abnormal contractions during the implantation period impair endometrial decidualization and contribute to infertility. John Wiley and Sons Inc. 2020-07-20 /pmc/articles/PMC7542020/ /pubmed/33071640 http://dx.doi.org/10.1002/rmb2.12341 Text en © 2020 The Authors. Reproductive Medicine and Biology published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Saito, Ryohei Kajihara, Takeshi Takamura, Masashi Tochigi, Hideno Sato, Tsuyoshi Ishihara, Osamu High stretch cycling inhibits the morphological and biological decidual process in human endometrial stromal cells |
title | High stretch cycling inhibits the morphological and biological decidual process in human endometrial stromal cells |
title_full | High stretch cycling inhibits the morphological and biological decidual process in human endometrial stromal cells |
title_fullStr | High stretch cycling inhibits the morphological and biological decidual process in human endometrial stromal cells |
title_full_unstemmed | High stretch cycling inhibits the morphological and biological decidual process in human endometrial stromal cells |
title_short | High stretch cycling inhibits the morphological and biological decidual process in human endometrial stromal cells |
title_sort | high stretch cycling inhibits the morphological and biological decidual process in human endometrial stromal cells |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542020/ https://www.ncbi.nlm.nih.gov/pubmed/33071640 http://dx.doi.org/10.1002/rmb2.12341 |
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