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Effects of Progesterone and 17β-Estradiol under Presence or Absence of FBS on Plasminogen Activators Activity in Porcine Uterine Epithelial Cells

The present study was conducted to investigate the regulatory mechanism of plasminogen activators (PAs) activation by 17β-estradiol (E(2)) and progesterone (P(4)) in porcine uterine epithelial cells (pUECs). pUECs were collected from porcine uterine horn and cultured at 80% confluence. Then, 0.1% (v...

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Autores principales: Hwangbo, Yong, Lee, Mi-Rim, Cheong, Hee-Tae, Yang, Boo-Keun, Park, Choon-Keun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Developmental Biology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344362/
https://www.ncbi.nlm.nih.gov/pubmed/30680330
http://dx.doi.org/10.12717/DR.2018.22.4.309
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author Hwangbo, Yong
Lee, Mi-Rim
Cheong, Hee-Tae
Yang, Boo-Keun
Park, Choon-Keun
author_facet Hwangbo, Yong
Lee, Mi-Rim
Cheong, Hee-Tae
Yang, Boo-Keun
Park, Choon-Keun
author_sort Hwangbo, Yong
collection PubMed
description The present study was conducted to investigate the regulatory mechanism of plasminogen activators (PAs) activation by 17β-estradiol (E(2)) and progesterone (P(4)) in porcine uterine epithelial cells (pUECs). pUECs were collected from porcine uterine horn and cultured at 80% confluence. Then, 0.1% (v/v) DMSO, 20 ng/mL E(2), and P(4) with or without fetal bovine serum (FBS) treated to cultured cells for 24 hours. The supernatants were used for measurement of PAs activity and expression of urokinase-type PA (uPA), tissue-type PA (tPA), uPA specific receptor (uPAR), and type-1 PA inhibitor (PAI-1) mRNA were analyzed by real-time PCR. The expression of PAs-related genes was not affect by steroid hormones in both of serum treatment groups. However, PAs activity was increased by treatment of E(2) compared to 0.1% DMSO treatment in serum-free group (p<0.05). Then, E(2) and P(4) were diluted with 0.002% (v/v) DMSO for reduction of its effect and treated to cultured cells without FBS. Only tPA mRNA was significantly increased by E(2) treatment (p<0.05). PAs activity was enhanced in E(2) treated group compared to control groups (p<0.05). These results indicate that serum-free condition is more proper to evaluate effect of steroid hormones and activation of PAs in pUECs was mainly regulated by estrogen. These regulation of PAs activation may be associated with uterine remodeling during pre-ovulatory phase in pigs, however, further studies are needed to investigate precise regulatory mechanism.
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spelling pubmed-63443622019-01-24 Effects of Progesterone and 17β-Estradiol under Presence or Absence of FBS on Plasminogen Activators Activity in Porcine Uterine Epithelial Cells Hwangbo, Yong Lee, Mi-Rim Cheong, Hee-Tae Yang, Boo-Keun Park, Choon-Keun Dev Reprod Original Research The present study was conducted to investigate the regulatory mechanism of plasminogen activators (PAs) activation by 17β-estradiol (E(2)) and progesterone (P(4)) in porcine uterine epithelial cells (pUECs). pUECs were collected from porcine uterine horn and cultured at 80% confluence. Then, 0.1% (v/v) DMSO, 20 ng/mL E(2), and P(4) with or without fetal bovine serum (FBS) treated to cultured cells for 24 hours. The supernatants were used for measurement of PAs activity and expression of urokinase-type PA (uPA), tissue-type PA (tPA), uPA specific receptor (uPAR), and type-1 PA inhibitor (PAI-1) mRNA were analyzed by real-time PCR. The expression of PAs-related genes was not affect by steroid hormones in both of serum treatment groups. However, PAs activity was increased by treatment of E(2) compared to 0.1% DMSO treatment in serum-free group (p<0.05). Then, E(2) and P(4) were diluted with 0.002% (v/v) DMSO for reduction of its effect and treated to cultured cells without FBS. Only tPA mRNA was significantly increased by E(2) treatment (p<0.05). PAs activity was enhanced in E(2) treated group compared to control groups (p<0.05). These results indicate that serum-free condition is more proper to evaluate effect of steroid hormones and activation of PAs in pUECs was mainly regulated by estrogen. These regulation of PAs activation may be associated with uterine remodeling during pre-ovulatory phase in pigs, however, further studies are needed to investigate precise regulatory mechanism. Korean Society of Developmental Biology 2018-12 2018-12-31 /pmc/articles/PMC6344362/ /pubmed/30680330 http://dx.doi.org/10.12717/DR.2018.22.4.309 Text en © Copyright 2018 The Korean Society of Developmental Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Hwangbo, Yong
Lee, Mi-Rim
Cheong, Hee-Tae
Yang, Boo-Keun
Park, Choon-Keun
Effects of Progesterone and 17β-Estradiol under Presence or Absence of FBS on Plasminogen Activators Activity in Porcine Uterine Epithelial Cells
title Effects of Progesterone and 17β-Estradiol under Presence or Absence of FBS on Plasminogen Activators Activity in Porcine Uterine Epithelial Cells
title_full Effects of Progesterone and 17β-Estradiol under Presence or Absence of FBS on Plasminogen Activators Activity in Porcine Uterine Epithelial Cells
title_fullStr Effects of Progesterone and 17β-Estradiol under Presence or Absence of FBS on Plasminogen Activators Activity in Porcine Uterine Epithelial Cells
title_full_unstemmed Effects of Progesterone and 17β-Estradiol under Presence or Absence of FBS on Plasminogen Activators Activity in Porcine Uterine Epithelial Cells
title_short Effects of Progesterone and 17β-Estradiol under Presence or Absence of FBS on Plasminogen Activators Activity in Porcine Uterine Epithelial Cells
title_sort effects of progesterone and 17β-estradiol under presence or absence of fbs on plasminogen activators activity in porcine uterine epithelial cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344362/
https://www.ncbi.nlm.nih.gov/pubmed/30680330
http://dx.doi.org/10.12717/DR.2018.22.4.309
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