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Selective segregation of DNA strands persists in long label retaining mammary cells during pregnancy

INTRODUCTION: During pregnancy the mammary epithelial compartment undergoes extreme proliferation and differentiation, facilitated by stem/progenitor cells. Mouse mammary epithelium in nonpregnant mice contains long label-retaining epithelial cells (LREC) that divide asymmetrically and retain their...

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Autores principales: Booth, Brian W, Boulanger, Corinne A, Smith, Gilbert H
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614527/
https://www.ncbi.nlm.nih.gov/pubmed/18950502
http://dx.doi.org/10.1186/bcr2188
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author Booth, Brian W
Boulanger, Corinne A
Smith, Gilbert H
author_facet Booth, Brian W
Boulanger, Corinne A
Smith, Gilbert H
author_sort Booth, Brian W
collection PubMed
description INTRODUCTION: During pregnancy the mammary epithelial compartment undergoes extreme proliferation and differentiation, facilitated by stem/progenitor cells. Mouse mammary epithelium in nonpregnant mice contains long label-retaining epithelial cells (LREC) that divide asymmetrically and retain their template DNA strands. The role of LREC during alveogenesis has not been determined. METHODS: We performed immunohistochemistry and autoradiography on murine mammary glands that had been labeled with 5-bromodeoxyuridine (5BrdU) during allometric ductal growth to investigate the co-expression of DNA label retention and estrogen receptor-α or progesterone receptor during pregnancy. A second DNA label ([(3)H]-thymidine) was administered during pregnancy to identify label-retaining cells (LRC), which subsequently enter the cell cycle. Use of this methodology allowed us to investigate the co-localization of 5BrdU with smooth muscle actin, CD31, cytokeratin, and desmin in periductal or peri-acinar LRC in mammary tissue from pregnant mice subsequent to a long chase period in order to identify LRC. RESULTS: Estrogen receptor-α positive and progesterone receptor positive cells represented approximately 30% to 40% of the LREC, which is under 1.0% of the epithelial subpopulation. Pregnancy altered the percentage of LREC expressing estrogen receptor-α. LRC situated in periductal or peri-acinar positions throughout the gland do not express epithelial, endothelial, or myoepithelial markers, and these undefined LRCs persist throughout pregnancy. Additionally, new cycling LREC ([(3)H]-thymidine retaining) appear during alveologenesis, and LRC found in other tissue types (for example, endothelium and nerve) within the mammary fat pad become double labeled during pregnancy, which indicates that they may also divide asymmetrically. CONCLUSIONS: Our findings support the premise that there is a subpopulation of LREC in the mouse mammary gland that persists during alveologenesis. These cells react to hormonal cues during pregnancy and enter the cell cycle while continuing to retain, selectively, their original template DNA. In addition, nonepithelial LRC are found in periductal or peri-acinar positions. These LRC also enter the cell cycle during pregnancy. During alveologenesis, newly created label-retaining ([(3)H]-thymidine) epithelial cells appear within the expanding alveoli and continue to cycle and retain their original template DNA ([(3)H]-thymidine) strands, as determined by a second pulse of 5BrdU.
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spelling pubmed-26145272009-01-08 Selective segregation of DNA strands persists in long label retaining mammary cells during pregnancy Booth, Brian W Boulanger, Corinne A Smith, Gilbert H Breast Cancer Res Research Article INTRODUCTION: During pregnancy the mammary epithelial compartment undergoes extreme proliferation and differentiation, facilitated by stem/progenitor cells. Mouse mammary epithelium in nonpregnant mice contains long label-retaining epithelial cells (LREC) that divide asymmetrically and retain their template DNA strands. The role of LREC during alveogenesis has not been determined. METHODS: We performed immunohistochemistry and autoradiography on murine mammary glands that had been labeled with 5-bromodeoxyuridine (5BrdU) during allometric ductal growth to investigate the co-expression of DNA label retention and estrogen receptor-α or progesterone receptor during pregnancy. A second DNA label ([(3)H]-thymidine) was administered during pregnancy to identify label-retaining cells (LRC), which subsequently enter the cell cycle. Use of this methodology allowed us to investigate the co-localization of 5BrdU with smooth muscle actin, CD31, cytokeratin, and desmin in periductal or peri-acinar LRC in mammary tissue from pregnant mice subsequent to a long chase period in order to identify LRC. RESULTS: Estrogen receptor-α positive and progesterone receptor positive cells represented approximately 30% to 40% of the LREC, which is under 1.0% of the epithelial subpopulation. Pregnancy altered the percentage of LREC expressing estrogen receptor-α. LRC situated in periductal or peri-acinar positions throughout the gland do not express epithelial, endothelial, or myoepithelial markers, and these undefined LRCs persist throughout pregnancy. Additionally, new cycling LREC ([(3)H]-thymidine retaining) appear during alveologenesis, and LRC found in other tissue types (for example, endothelium and nerve) within the mammary fat pad become double labeled during pregnancy, which indicates that they may also divide asymmetrically. CONCLUSIONS: Our findings support the premise that there is a subpopulation of LREC in the mouse mammary gland that persists during alveologenesis. These cells react to hormonal cues during pregnancy and enter the cell cycle while continuing to retain, selectively, their original template DNA. In addition, nonepithelial LRC are found in periductal or peri-acinar positions. These LRC also enter the cell cycle during pregnancy. During alveologenesis, newly created label-retaining ([(3)H]-thymidine) epithelial cells appear within the expanding alveoli and continue to cycle and retain their original template DNA ([(3)H]-thymidine) strands, as determined by a second pulse of 5BrdU. BioMed Central 2008 2008-10-24 /pmc/articles/PMC2614527/ /pubmed/18950502 http://dx.doi.org/10.1186/bcr2188 Text en Copyright © 2008 Booth 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 Research Article
Booth, Brian W
Boulanger, Corinne A
Smith, Gilbert H
Selective segregation of DNA strands persists in long label retaining mammary cells during pregnancy
title Selective segregation of DNA strands persists in long label retaining mammary cells during pregnancy
title_full Selective segregation of DNA strands persists in long label retaining mammary cells during pregnancy
title_fullStr Selective segregation of DNA strands persists in long label retaining mammary cells during pregnancy
title_full_unstemmed Selective segregation of DNA strands persists in long label retaining mammary cells during pregnancy
title_short Selective segregation of DNA strands persists in long label retaining mammary cells during pregnancy
title_sort selective segregation of dna strands persists in long label retaining mammary cells during pregnancy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614527/
https://www.ncbi.nlm.nih.gov/pubmed/18950502
http://dx.doi.org/10.1186/bcr2188
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