Cargando…
HB-EGF upregulates StAR expression and stimulates progesterone production through ERK1/2 signaling in human granulosa-lutein cells
BACKGROUND: Heparin-binding epidermal growth factor-like growth factor (HB-EGF) belongs to the epidermal growth factor (EGF) family of growth factors. HB-EGF and its receptors, epidermal growth factor receptor (EGFR) and HER4, are expressed in the human corpus luteum. HB-EGF has been shown to regula...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598000/ https://www.ncbi.nlm.nih.gov/pubmed/36284301 http://dx.doi.org/10.1186/s12964-022-00983-4 |
_version_ | 1784816225398816768 |
---|---|
author | Cheng, Jung-Chien Han, Xiaoyu Meng, Qingxue Guo, Yanjie Liu, Boqun Song, Tinglin Jia, Yuanyuan Fang, Lanlan Sun, Ying-Pu |
author_facet | Cheng, Jung-Chien Han, Xiaoyu Meng, Qingxue Guo, Yanjie Liu, Boqun Song, Tinglin Jia, Yuanyuan Fang, Lanlan Sun, Ying-Pu |
author_sort | Cheng, Jung-Chien |
collection | PubMed |
description | BACKGROUND: Heparin-binding epidermal growth factor-like growth factor (HB-EGF) belongs to the epidermal growth factor (EGF) family of growth factors. HB-EGF and its receptors, epidermal growth factor receptor (EGFR) and HER4, are expressed in the human corpus luteum. HB-EGF has been shown to regulate luteal function by preventing cell apoptosis. Steroidogenesis is the primary function of the human corpus luteum. Steroidogenic acute regulatory protein (StAR) plays a critical role in steroidogenesis. StAR expression and progesterone (P4) production in human granulosa-lutein (hGL) cells have been shown to be upregulated by a ligand of EGFR, amphiregulin. However, whether HB-EGF can achieve the same effects remains unknown. METHODS: A steroidogenic human ovarian granulosa-like tumor cell line, KGN, and primary culture of hGL cells obtained from patients undergoing in vitro fertilization treatment were used as experimental models. The underlying molecular mechanisms mediating the effects of HB-EGF on StAR expression and P4 production were explored by a series of in vitro experiments. RESULTS: Western blot showed that EGFR, HER2, and HER4 were expressed in both KGN and hGL cells. Treatment with HB-EGF for 24 h induced StAR expression but did not affect the expression of steroidogenesis-related enzymes, P450 side chain cleavage enzyme, 3β-hydroxysteroid dehydrogenase, and aromatase. Using pharmacological inhibitors and a siRNA-mediated knockdown approach, we showed that EGFR, HER4, but not HER2, were required for HB-EGF-stimulated StAR expression and P4 production. In addition, HB-EGF-induced upregulations of StAR expression and P4 production were mediated by the activation of the ERK1/2 signaling pathway. CONCLUSION: This study increases the understanding of the physiological role of HB-EGF in human luteal functions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-022-00983-4. |
format | Online Article Text |
id | pubmed-9598000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95980002022-10-27 HB-EGF upregulates StAR expression and stimulates progesterone production through ERK1/2 signaling in human granulosa-lutein cells Cheng, Jung-Chien Han, Xiaoyu Meng, Qingxue Guo, Yanjie Liu, Boqun Song, Tinglin Jia, Yuanyuan Fang, Lanlan Sun, Ying-Pu Cell Commun Signal Research BACKGROUND: Heparin-binding epidermal growth factor-like growth factor (HB-EGF) belongs to the epidermal growth factor (EGF) family of growth factors. HB-EGF and its receptors, epidermal growth factor receptor (EGFR) and HER4, are expressed in the human corpus luteum. HB-EGF has been shown to regulate luteal function by preventing cell apoptosis. Steroidogenesis is the primary function of the human corpus luteum. Steroidogenic acute regulatory protein (StAR) plays a critical role in steroidogenesis. StAR expression and progesterone (P4) production in human granulosa-lutein (hGL) cells have been shown to be upregulated by a ligand of EGFR, amphiregulin. However, whether HB-EGF can achieve the same effects remains unknown. METHODS: A steroidogenic human ovarian granulosa-like tumor cell line, KGN, and primary culture of hGL cells obtained from patients undergoing in vitro fertilization treatment were used as experimental models. The underlying molecular mechanisms mediating the effects of HB-EGF on StAR expression and P4 production were explored by a series of in vitro experiments. RESULTS: Western blot showed that EGFR, HER2, and HER4 were expressed in both KGN and hGL cells. Treatment with HB-EGF for 24 h induced StAR expression but did not affect the expression of steroidogenesis-related enzymes, P450 side chain cleavage enzyme, 3β-hydroxysteroid dehydrogenase, and aromatase. Using pharmacological inhibitors and a siRNA-mediated knockdown approach, we showed that EGFR, HER4, but not HER2, were required for HB-EGF-stimulated StAR expression and P4 production. In addition, HB-EGF-induced upregulations of StAR expression and P4 production were mediated by the activation of the ERK1/2 signaling pathway. CONCLUSION: This study increases the understanding of the physiological role of HB-EGF in human luteal functions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-022-00983-4. BioMed Central 2022-10-25 /pmc/articles/PMC9598000/ /pubmed/36284301 http://dx.doi.org/10.1186/s12964-022-00983-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Cheng, Jung-Chien Han, Xiaoyu Meng, Qingxue Guo, Yanjie Liu, Boqun Song, Tinglin Jia, Yuanyuan Fang, Lanlan Sun, Ying-Pu HB-EGF upregulates StAR expression and stimulates progesterone production through ERK1/2 signaling in human granulosa-lutein cells |
title | HB-EGF upregulates StAR expression and stimulates progesterone production through ERK1/2 signaling in human granulosa-lutein cells |
title_full | HB-EGF upregulates StAR expression and stimulates progesterone production through ERK1/2 signaling in human granulosa-lutein cells |
title_fullStr | HB-EGF upregulates StAR expression and stimulates progesterone production through ERK1/2 signaling in human granulosa-lutein cells |
title_full_unstemmed | HB-EGF upregulates StAR expression and stimulates progesterone production through ERK1/2 signaling in human granulosa-lutein cells |
title_short | HB-EGF upregulates StAR expression and stimulates progesterone production through ERK1/2 signaling in human granulosa-lutein cells |
title_sort | hb-egf upregulates star expression and stimulates progesterone production through erk1/2 signaling in human granulosa-lutein cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598000/ https://www.ncbi.nlm.nih.gov/pubmed/36284301 http://dx.doi.org/10.1186/s12964-022-00983-4 |
work_keys_str_mv | AT chengjungchien hbegfupregulatesstarexpressionandstimulatesprogesteroneproductionthrougherk12signalinginhumangranulosaluteincells AT hanxiaoyu hbegfupregulatesstarexpressionandstimulatesprogesteroneproductionthrougherk12signalinginhumangranulosaluteincells AT mengqingxue hbegfupregulatesstarexpressionandstimulatesprogesteroneproductionthrougherk12signalinginhumangranulosaluteincells AT guoyanjie hbegfupregulatesstarexpressionandstimulatesprogesteroneproductionthrougherk12signalinginhumangranulosaluteincells AT liuboqun hbegfupregulatesstarexpressionandstimulatesprogesteroneproductionthrougherk12signalinginhumangranulosaluteincells AT songtinglin hbegfupregulatesstarexpressionandstimulatesprogesteroneproductionthrougherk12signalinginhumangranulosaluteincells AT jiayuanyuan hbegfupregulatesstarexpressionandstimulatesprogesteroneproductionthrougherk12signalinginhumangranulosaluteincells AT fanglanlan hbegfupregulatesstarexpressionandstimulatesprogesteroneproductionthrougherk12signalinginhumangranulosaluteincells AT sunyingpu hbegfupregulatesstarexpressionandstimulatesprogesteroneproductionthrougherk12signalinginhumangranulosaluteincells |