Mechanism of progesterone promoting uterine smooth muscle contraction through RhoA/ROCK signaling pathway

Objective To investigate the mechanism of progesterone affecting the contractions of uterine smooth muscle through RhoA/ROCK signaling pathway. Methods The tissues of uterine smooth muscle were collected from 5 cases in labor and another 5 of non-labor, respectively. The expression levels of phospho...

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Main Authors: YAN Xiaoli, CHEN Cheng, WANG Dan, CHANG Qing
Format: Article
Language:zho
Published: Editorial Office of Journal of Army Medical University 2022-06-01
Series:陆军军医大学学报
Subjects:
Online Access:http://aammt.tmmu.edu.cn/Upload/rhtml/202111235.htm
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author YAN Xiaoli
CHEN Cheng
WANG Dan
CHANG Qing
author_facet YAN Xiaoli
CHEN Cheng
WANG Dan
CHANG Qing
author_sort YAN Xiaoli
collection DOAJ
description Objective To investigate the mechanism of progesterone affecting the contractions of uterine smooth muscle through RhoA/ROCK signaling pathway. Methods The tissues of uterine smooth muscle were collected from 5 cases in labor and another 5 of non-labor, respectively. The expression levels of phosphorylation of myosin light chain (p-MLC20), ROCK1 and ROCK2 were detected by Western blotting and immunohistochemical (IHC) assay. Uterine smooth muscle cells were isolated and cultured, and then identified by immunofluorescence assay. Laser confocal microscopy was used to measure the concentration of intracellular free Ca2+ ([Ca2+]i) in the cells. In addition, the uterine smooth muscle cells were treated with progesterone+progesterone receptor antagonist, mifepristone, and with progesterone+ROCK inhibitor, Y-27632, respectively. Western blotting was performed to determine the expression of p-MLC20, ROCK1 and ROCK2 in the corresponding groups. Results As compared with the non-labor group, the expression of p-MLC20, ROCK1 and ROCK2 in the uterine smooth muscle tissues were significantly increased in the labor group (P < 0.05). Progesterone induced the elevation of p-MLC20, ROCK1 and ROCK2 levels in the cultured uterine smooth muscle cells (P < 0.05), while after the intervention of Y-27632+progesterone, the p-MLC20 level was greatly decreased (P < 0.05). Conclusion Progesterone regulates p-MLC20 level through RhoA/ROCK signaling pathway and thus promotes the contractions of uterine smooth muscle cells.
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spelling doaj.art-ad6e8cbea1bb47edbc41e99f9b3de9152022-12-22T00:32:33ZzhoEditorial Office of Journal of Army Medical University陆军军医大学学报2097-09272022-06-0144121199120610.16016/j.2097-0927.202111235Mechanism of progesterone promoting uterine smooth muscle contraction through RhoA/ROCK signaling pathwayYAN Xiaoli0CHEN Cheng1WANG Dan2CHANG Qing3 Department of Gynecology and Obstetrics, First Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, 400038Department of Gynecology and Obstetrics, Chongqing Hospital of University of Chinese Academy of Sciences (Chongqing General Hospital), Chongqing, 401147, ChinaDepartment of Gynecology and Obstetrics, First Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, 400038Department of Gynecology and Obstetrics, First Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, 400038Objective To investigate the mechanism of progesterone affecting the contractions of uterine smooth muscle through RhoA/ROCK signaling pathway. Methods The tissues of uterine smooth muscle were collected from 5 cases in labor and another 5 of non-labor, respectively. The expression levels of phosphorylation of myosin light chain (p-MLC20), ROCK1 and ROCK2 were detected by Western blotting and immunohistochemical (IHC) assay. Uterine smooth muscle cells were isolated and cultured, and then identified by immunofluorescence assay. Laser confocal microscopy was used to measure the concentration of intracellular free Ca2+ ([Ca2+]i) in the cells. In addition, the uterine smooth muscle cells were treated with progesterone+progesterone receptor antagonist, mifepristone, and with progesterone+ROCK inhibitor, Y-27632, respectively. Western blotting was performed to determine the expression of p-MLC20, ROCK1 and ROCK2 in the corresponding groups. Results As compared with the non-labor group, the expression of p-MLC20, ROCK1 and ROCK2 in the uterine smooth muscle tissues were significantly increased in the labor group (P < 0.05). Progesterone induced the elevation of p-MLC20, ROCK1 and ROCK2 levels in the cultured uterine smooth muscle cells (P < 0.05), while after the intervention of Y-27632+progesterone, the p-MLC20 level was greatly decreased (P < 0.05). Conclusion Progesterone regulates p-MLC20 level through RhoA/ROCK signaling pathway and thus promotes the contractions of uterine smooth muscle cells. http://aammt.tmmu.edu.cn/Upload/rhtml/202111235.htmprogesteronerhoa/rock signal pathwayphosphorylation of myosin light chain 20 uterine contractionsmooth muscle cells
spellingShingle YAN Xiaoli
CHEN Cheng
WANG Dan
CHANG Qing
Mechanism of progesterone promoting uterine smooth muscle contraction through RhoA/ROCK signaling pathway
陆军军医大学学报
progesterone
rhoa/rock signal pathway
phosphorylation of myosin light chain 20 uterine contraction
smooth muscle cells
title Mechanism of progesterone promoting uterine smooth muscle contraction through RhoA/ROCK signaling pathway
title_full Mechanism of progesterone promoting uterine smooth muscle contraction through RhoA/ROCK signaling pathway
title_fullStr Mechanism of progesterone promoting uterine smooth muscle contraction through RhoA/ROCK signaling pathway
title_full_unstemmed Mechanism of progesterone promoting uterine smooth muscle contraction through RhoA/ROCK signaling pathway
title_short Mechanism of progesterone promoting uterine smooth muscle contraction through RhoA/ROCK signaling pathway
title_sort mechanism of progesterone promoting uterine smooth muscle contraction through rhoa rock signaling pathway
topic progesterone
rhoa/rock signal pathway
phosphorylation of myosin light chain 20 uterine contraction
smooth muscle cells
url http://aammt.tmmu.edu.cn/Upload/rhtml/202111235.htm
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AT chencheng mechanismofprogesteronepromotinguterinesmoothmusclecontractionthroughrhoarocksignalingpathway
AT wangdan mechanismofprogesteronepromotinguterinesmoothmusclecontractionthroughrhoarocksignalingpathway
AT changqing mechanismofprogesteronepromotinguterinesmoothmusclecontractionthroughrhoarocksignalingpathway