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Reelin and aromatase cooperate in ovarian follicle development
Reelin plays an important role in cerebral cortex development and synaptogenesis. In the hippocampus, the neurosteroid estrogen affects reelin expression. In this study we tested a potential crosstalk between estradiol and reelin, thus the possibility of a reelin-induced activation of the estradiol...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992190/ https://www.ncbi.nlm.nih.gov/pubmed/29880879 http://dx.doi.org/10.1038/s41598-018-26928-x |
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author | Meseke, Maurice Pröls, Felicitas Schmahl, Camilla Seebo, Katja Kruse, Claas Brandt, Nicola Fester, Lars Zhou, Lepu Bender, Roland Rune, Gabriele M. |
author_facet | Meseke, Maurice Pröls, Felicitas Schmahl, Camilla Seebo, Katja Kruse, Claas Brandt, Nicola Fester, Lars Zhou, Lepu Bender, Roland Rune, Gabriele M. |
author_sort | Meseke, Maurice |
collection | PubMed |
description | Reelin plays an important role in cerebral cortex development and synaptogenesis. In the hippocampus, the neurosteroid estrogen affects reelin expression. In this study we tested a potential crosstalk between estradiol and reelin, thus the possibility of a reelin-induced activation of the estradiol synthesizing enzyme aromatase. As a model system, we used ovaries, which express reelin and are a major source of estradiol. We found that in wild-type mice, reelin and aromatase are expressed in granulosa cells of growing follicles. The expression of reelin varies with the estrus cycle and is highest shortly before ovulation, when estradiol serum levels are at their maximum. In ovaries of reelin-deficient reeler mice, aromatase mRNA and protein are significantly reduced, as evidenced by real-time PCR, western blot analysis, and quantitative immunohistochemistry in granulosa cells of preovulatory follicles. In line with reduced estradiol synthesis, ovarian estrus cycle length is prolonged in reeler mice. Most importantly, treating cultured granulosa cells with recombinant reelin results in significant upregulation of aromatase mRNA and protein and increased secretion of estradiol into the supernatant. Our data provide evidence of a local increase of aromatase expression by reelin. Regarding reproduction, this crosstalk may contribute to follicular stability and counteract luteinization in ovaries. |
format | Online Article Text |
id | pubmed-5992190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59921902018-07-05 Reelin and aromatase cooperate in ovarian follicle development Meseke, Maurice Pröls, Felicitas Schmahl, Camilla Seebo, Katja Kruse, Claas Brandt, Nicola Fester, Lars Zhou, Lepu Bender, Roland Rune, Gabriele M. Sci Rep Article Reelin plays an important role in cerebral cortex development and synaptogenesis. In the hippocampus, the neurosteroid estrogen affects reelin expression. In this study we tested a potential crosstalk between estradiol and reelin, thus the possibility of a reelin-induced activation of the estradiol synthesizing enzyme aromatase. As a model system, we used ovaries, which express reelin and are a major source of estradiol. We found that in wild-type mice, reelin and aromatase are expressed in granulosa cells of growing follicles. The expression of reelin varies with the estrus cycle and is highest shortly before ovulation, when estradiol serum levels are at their maximum. In ovaries of reelin-deficient reeler mice, aromatase mRNA and protein are significantly reduced, as evidenced by real-time PCR, western blot analysis, and quantitative immunohistochemistry in granulosa cells of preovulatory follicles. In line with reduced estradiol synthesis, ovarian estrus cycle length is prolonged in reeler mice. Most importantly, treating cultured granulosa cells with recombinant reelin results in significant upregulation of aromatase mRNA and protein and increased secretion of estradiol into the supernatant. Our data provide evidence of a local increase of aromatase expression by reelin. Regarding reproduction, this crosstalk may contribute to follicular stability and counteract luteinization in ovaries. Nature Publishing Group UK 2018-06-07 /pmc/articles/PMC5992190/ /pubmed/29880879 http://dx.doi.org/10.1038/s41598-018-26928-x Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Meseke, Maurice Pröls, Felicitas Schmahl, Camilla Seebo, Katja Kruse, Claas Brandt, Nicola Fester, Lars Zhou, Lepu Bender, Roland Rune, Gabriele M. Reelin and aromatase cooperate in ovarian follicle development |
title | Reelin and aromatase cooperate in ovarian follicle development |
title_full | Reelin and aromatase cooperate in ovarian follicle development |
title_fullStr | Reelin and aromatase cooperate in ovarian follicle development |
title_full_unstemmed | Reelin and aromatase cooperate in ovarian follicle development |
title_short | Reelin and aromatase cooperate in ovarian follicle development |
title_sort | reelin and aromatase cooperate in ovarian follicle development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992190/ https://www.ncbi.nlm.nih.gov/pubmed/29880879 http://dx.doi.org/10.1038/s41598-018-26928-x |
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