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Whole ovary immunohistochemistry for monitoring cell proliferation and ovulatory wound repair in the mouse

BACKGROUND: Ovarian surface epithelial cells are thought to be a precursor cell type for ovarian carcinoma. It has been proposed that an increased rate of ovarian surface epithelial cell proliferation during ovulatory wound repair contributes to the accumulation of genetic changes and cell transform...

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Autores principales: Singavarapu, Rajasekhar, Buchinsky, Natalie, Cheon, Dong-Joo, Orsulic, Sandra
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2929235/
https://www.ncbi.nlm.nih.gov/pubmed/20712898
http://dx.doi.org/10.1186/1477-7827-8-98
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author Singavarapu, Rajasekhar
Buchinsky, Natalie
Cheon, Dong-Joo
Orsulic, Sandra
author_facet Singavarapu, Rajasekhar
Buchinsky, Natalie
Cheon, Dong-Joo
Orsulic, Sandra
author_sort Singavarapu, Rajasekhar
collection PubMed
description BACKGROUND: Ovarian surface epithelial cells are thought to be a precursor cell type for ovarian carcinoma. It has been proposed that an increased rate of ovarian surface epithelial cell proliferation during ovulatory wound repair contributes to the accumulation of genetic changes and cell transformation. The proliferation of ovarian surface epithelial cells during ovulatory wound repair has been studied primarily using immunohistochemical staining of paraffin-embedded ovary sections. However, such analyses require complex reconstruction from serially-cut ovary sections for the visualization and quantification of the cells on the ovarian surface. In order to directly visualize the proliferation and organization of the ovarian surface epithelial cells, we developed a technique for immunohistochemical staining of whole mouse ovaries. Using this method, we analyzed cell proliferation and morphologic changes in mouse ovarian surface epithelial cells during follicle growth and ovulatory wound repair. METHODS: Three-week old FVB/N female mice were superovulated by sequential administration of pregnant mare's serum gonadotropin (PMSG) and human chorionic gonadotropin (hCG). Ten hours after hCG administration, mice were given 5-bromo-2-deoxyuridine (BrdU) and euthanized two hours after BrdU administration for ovary isolation. The levels of incorporated BrdU in the ovarian surface epithelial cells were measured by staining paraffin-embedded ovary sections and whole ovaries with the BrdU antibody. Re-epithelialization of the ovarian surface after ovulatory rupture was visualized by immunohistochemical staining with E-cadherin and Keratin 8 in paraffin-embedded ovary sections and whole ovaries. RESULTS: We determined that active proliferation of ovarian epithelial surface cells primarily occurs during antral follicle formation and, to a lesser extent, in response to an ovulatory wound. We also demonstrated that ovarian surface epithelial cells exhibit a circular organization around the wound site CONCLUSION: Whole ovary immunohistochemistry enables efficient and comprehensive three-dimensional visualization of ovarian surface epithelial cells without the need for laborious reconstruction from immunohistochemically-stained serial ovary sections.
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spelling pubmed-29292352010-08-28 Whole ovary immunohistochemistry for monitoring cell proliferation and ovulatory wound repair in the mouse Singavarapu, Rajasekhar Buchinsky, Natalie Cheon, Dong-Joo Orsulic, Sandra Reprod Biol Endocrinol Methodology BACKGROUND: Ovarian surface epithelial cells are thought to be a precursor cell type for ovarian carcinoma. It has been proposed that an increased rate of ovarian surface epithelial cell proliferation during ovulatory wound repair contributes to the accumulation of genetic changes and cell transformation. The proliferation of ovarian surface epithelial cells during ovulatory wound repair has been studied primarily using immunohistochemical staining of paraffin-embedded ovary sections. However, such analyses require complex reconstruction from serially-cut ovary sections for the visualization and quantification of the cells on the ovarian surface. In order to directly visualize the proliferation and organization of the ovarian surface epithelial cells, we developed a technique for immunohistochemical staining of whole mouse ovaries. Using this method, we analyzed cell proliferation and morphologic changes in mouse ovarian surface epithelial cells during follicle growth and ovulatory wound repair. METHODS: Three-week old FVB/N female mice were superovulated by sequential administration of pregnant mare's serum gonadotropin (PMSG) and human chorionic gonadotropin (hCG). Ten hours after hCG administration, mice were given 5-bromo-2-deoxyuridine (BrdU) and euthanized two hours after BrdU administration for ovary isolation. The levels of incorporated BrdU in the ovarian surface epithelial cells were measured by staining paraffin-embedded ovary sections and whole ovaries with the BrdU antibody. Re-epithelialization of the ovarian surface after ovulatory rupture was visualized by immunohistochemical staining with E-cadherin and Keratin 8 in paraffin-embedded ovary sections and whole ovaries. RESULTS: We determined that active proliferation of ovarian epithelial surface cells primarily occurs during antral follicle formation and, to a lesser extent, in response to an ovulatory wound. We also demonstrated that ovarian surface epithelial cells exhibit a circular organization around the wound site CONCLUSION: Whole ovary immunohistochemistry enables efficient and comprehensive three-dimensional visualization of ovarian surface epithelial cells without the need for laborious reconstruction from immunohistochemically-stained serial ovary sections. BioMed Central 2010-08-16 /pmc/articles/PMC2929235/ /pubmed/20712898 http://dx.doi.org/10.1186/1477-7827-8-98 Text en Copyright ©2010 Singavarapu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Singavarapu, Rajasekhar
Buchinsky, Natalie
Cheon, Dong-Joo
Orsulic, Sandra
Whole ovary immunohistochemistry for monitoring cell proliferation and ovulatory wound repair in the mouse
title Whole ovary immunohistochemistry for monitoring cell proliferation and ovulatory wound repair in the mouse
title_full Whole ovary immunohistochemistry for monitoring cell proliferation and ovulatory wound repair in the mouse
title_fullStr Whole ovary immunohistochemistry for monitoring cell proliferation and ovulatory wound repair in the mouse
title_full_unstemmed Whole ovary immunohistochemistry for monitoring cell proliferation and ovulatory wound repair in the mouse
title_short Whole ovary immunohistochemistry for monitoring cell proliferation and ovulatory wound repair in the mouse
title_sort whole ovary immunohistochemistry for monitoring cell proliferation and ovulatory wound repair in the mouse
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2929235/
https://www.ncbi.nlm.nih.gov/pubmed/20712898
http://dx.doi.org/10.1186/1477-7827-8-98
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