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Identification of germ cell-specific VASA and IFITM3 proteins in human ovarian endometriosis

BACKGROUND: Endometriosis is a gynaecological disorder that affects 6–10 % of female population. It is characterized by the presence of endometrial tissue outside the uterus, most often in the pelvic peritoneum or ovaries. Recent studies have indicated that mesenchymal endometrial stem cells might g...

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Autores principales: Fraunhoffer, Nicolas A., Meilerman Abuelafia, Analía, Stella, Inés, Galliano, Silvia, Barrios, Marcela, Vitullo, Alfredo D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597381/
https://www.ncbi.nlm.nih.gov/pubmed/26446766
http://dx.doi.org/10.1186/s13048-015-0193-8
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author Fraunhoffer, Nicolas A.
Meilerman Abuelafia, Analía
Stella, Inés
Galliano, Silvia
Barrios, Marcela
Vitullo, Alfredo D.
author_facet Fraunhoffer, Nicolas A.
Meilerman Abuelafia, Analía
Stella, Inés
Galliano, Silvia
Barrios, Marcela
Vitullo, Alfredo D.
author_sort Fraunhoffer, Nicolas A.
collection PubMed
description BACKGROUND: Endometriosis is a gynaecological disorder that affects 6–10 % of female population. It is characterized by the presence of endometrial tissue outside the uterus, most often in the pelvic peritoneum or ovaries. Recent studies have indicated that mesenchymal endometrial stem cells might get involved in endometriosis progression. Although germ line stem cells have been proved to exist in the ovary, their involvement in ovarian endometriosis has not been investigated. In this preliminary report we aimed to identify germinal stem cell markers in ovarian endometriosis. FINDINGS: Ten paraffin-embedded ovarian endometriosis samples were screened for germ cell-specific proteins DDX4 (VASA) and IFITM3, and its relation with stem cell marker OCT4, proliferation marker PCNA and estrogen receptor alpha (ESR1), by immunohistochemistry, immunofluorescence and PCR. DDX4 and IFITM3 proteins were expressed in isolated cells and clusters of cells in the cortical region of ovarian endometriotic cysts. DDX4 and IFITM3 co-localized in cells from endometriotic stroma, and DDX4/IFITM3-expressing cells were positive for ESR1, OCT4 and PCNA. No cells expressing neither DDX4 nor IFITM3 were detected in normal endometrial tissue. CONCLUSION: The identification of germ cell-specific proteins DDX4 and IFITM3 provides the first evidence of ovarian-sourced cells in ovarian endometriotic lesions and opens up new directions towards understanding the still confusing pathogenesis of endometriosis.
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spelling pubmed-45973812015-10-08 Identification of germ cell-specific VASA and IFITM3 proteins in human ovarian endometriosis Fraunhoffer, Nicolas A. Meilerman Abuelafia, Analía Stella, Inés Galliano, Silvia Barrios, Marcela Vitullo, Alfredo D. J Ovarian Res Brief Communication BACKGROUND: Endometriosis is a gynaecological disorder that affects 6–10 % of female population. It is characterized by the presence of endometrial tissue outside the uterus, most often in the pelvic peritoneum or ovaries. Recent studies have indicated that mesenchymal endometrial stem cells might get involved in endometriosis progression. Although germ line stem cells have been proved to exist in the ovary, their involvement in ovarian endometriosis has not been investigated. In this preliminary report we aimed to identify germinal stem cell markers in ovarian endometriosis. FINDINGS: Ten paraffin-embedded ovarian endometriosis samples were screened for germ cell-specific proteins DDX4 (VASA) and IFITM3, and its relation with stem cell marker OCT4, proliferation marker PCNA and estrogen receptor alpha (ESR1), by immunohistochemistry, immunofluorescence and PCR. DDX4 and IFITM3 proteins were expressed in isolated cells and clusters of cells in the cortical region of ovarian endometriotic cysts. DDX4 and IFITM3 co-localized in cells from endometriotic stroma, and DDX4/IFITM3-expressing cells were positive for ESR1, OCT4 and PCNA. No cells expressing neither DDX4 nor IFITM3 were detected in normal endometrial tissue. CONCLUSION: The identification of germ cell-specific proteins DDX4 and IFITM3 provides the first evidence of ovarian-sourced cells in ovarian endometriotic lesions and opens up new directions towards understanding the still confusing pathogenesis of endometriosis. BioMed Central 2015-10-07 /pmc/articles/PMC4597381/ /pubmed/26446766 http://dx.doi.org/10.1186/s13048-015-0193-8 Text en © Fraunhoffer et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Brief Communication
Fraunhoffer, Nicolas A.
Meilerman Abuelafia, Analía
Stella, Inés
Galliano, Silvia
Barrios, Marcela
Vitullo, Alfredo D.
Identification of germ cell-specific VASA and IFITM3 proteins in human ovarian endometriosis
title Identification of germ cell-specific VASA and IFITM3 proteins in human ovarian endometriosis
title_full Identification of germ cell-specific VASA and IFITM3 proteins in human ovarian endometriosis
title_fullStr Identification of germ cell-specific VASA and IFITM3 proteins in human ovarian endometriosis
title_full_unstemmed Identification of germ cell-specific VASA and IFITM3 proteins in human ovarian endometriosis
title_short Identification of germ cell-specific VASA and IFITM3 proteins in human ovarian endometriosis
title_sort identification of germ cell-specific vasa and ifitm3 proteins in human ovarian endometriosis
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597381/
https://www.ncbi.nlm.nih.gov/pubmed/26446766
http://dx.doi.org/10.1186/s13048-015-0193-8
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