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Loss of Panx1 Impairs Mammary Gland Development at Lactation: Implications for Breast Tumorigenesis

Pannexin1 (Panx1) subunits oligomerize to form large-pore channels between the intracellular and extracellular milieu that have been shown to regulate proliferation, differentiation and cell death mechanisms. These key cellular responses are ultimately necessary for normal tissue development and fun...

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Autores principales: Stewart, Michael K. G., Plante, Isabelle, Penuela, Silvia, Laird, Dale W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839729/
https://www.ncbi.nlm.nih.gov/pubmed/27099931
http://dx.doi.org/10.1371/journal.pone.0154162
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author Stewart, Michael K. G.
Plante, Isabelle
Penuela, Silvia
Laird, Dale W.
author_facet Stewart, Michael K. G.
Plante, Isabelle
Penuela, Silvia
Laird, Dale W.
author_sort Stewart, Michael K. G.
collection PubMed
description Pannexin1 (Panx1) subunits oligomerize to form large-pore channels between the intracellular and extracellular milieu that have been shown to regulate proliferation, differentiation and cell death mechanisms. These key cellular responses are ultimately necessary for normal tissue development and function but the role of Panx1 in development, differentiation and function in many tissues remains unexplored, including that of the breast. Panx1 was identified to be expressed in the mammary gland through western blot and immunofluorescent analysis and is dynamically upregulated during pregnancy and lactation. In order to evaluate the role of Panx1 in the context of mammary gland development and function, Panx1(-/-) mice were evaluated in comparison to wild-type mice in the mammary glands of virgin, lactating and involuting mice. Our results revealed that Panx1 ablation did not affect virgin or involuting mammary glands following histological and whole mount analysis. Panx1 was necessary for timely alveolar development during early lactation based on a decreased number of alveolar lumen following histological analysis and reduced proliferation following Ki67 immunofluorescent labelling. Importantly, the loss of Panx1 in lactating mammary glands did not overtly affect epithelial or secretory differentiation of the mammary gland suggesting that Panx1 is not critical in normal mammary gland function. In addition, PANX1 mRNA expression was correlated with negative clinical outcomes in patients with breast cancer using in silico arrays. Together, our results suggest that Panx1 is necessary for timely alveolar development following the transition from pregnancy to lactation, which may have implications extending to patients with breast cancer.
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spelling pubmed-48397292016-04-29 Loss of Panx1 Impairs Mammary Gland Development at Lactation: Implications for Breast Tumorigenesis Stewart, Michael K. G. Plante, Isabelle Penuela, Silvia Laird, Dale W. PLoS One Research Article Pannexin1 (Panx1) subunits oligomerize to form large-pore channels between the intracellular and extracellular milieu that have been shown to regulate proliferation, differentiation and cell death mechanisms. These key cellular responses are ultimately necessary for normal tissue development and function but the role of Panx1 in development, differentiation and function in many tissues remains unexplored, including that of the breast. Panx1 was identified to be expressed in the mammary gland through western blot and immunofluorescent analysis and is dynamically upregulated during pregnancy and lactation. In order to evaluate the role of Panx1 in the context of mammary gland development and function, Panx1(-/-) mice were evaluated in comparison to wild-type mice in the mammary glands of virgin, lactating and involuting mice. Our results revealed that Panx1 ablation did not affect virgin or involuting mammary glands following histological and whole mount analysis. Panx1 was necessary for timely alveolar development during early lactation based on a decreased number of alveolar lumen following histological analysis and reduced proliferation following Ki67 immunofluorescent labelling. Importantly, the loss of Panx1 in lactating mammary glands did not overtly affect epithelial or secretory differentiation of the mammary gland suggesting that Panx1 is not critical in normal mammary gland function. In addition, PANX1 mRNA expression was correlated with negative clinical outcomes in patients with breast cancer using in silico arrays. Together, our results suggest that Panx1 is necessary for timely alveolar development following the transition from pregnancy to lactation, which may have implications extending to patients with breast cancer. Public Library of Science 2016-04-21 /pmc/articles/PMC4839729/ /pubmed/27099931 http://dx.doi.org/10.1371/journal.pone.0154162 Text en © 2016 Stewart et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Stewart, Michael K. G.
Plante, Isabelle
Penuela, Silvia
Laird, Dale W.
Loss of Panx1 Impairs Mammary Gland Development at Lactation: Implications for Breast Tumorigenesis
title Loss of Panx1 Impairs Mammary Gland Development at Lactation: Implications for Breast Tumorigenesis
title_full Loss of Panx1 Impairs Mammary Gland Development at Lactation: Implications for Breast Tumorigenesis
title_fullStr Loss of Panx1 Impairs Mammary Gland Development at Lactation: Implications for Breast Tumorigenesis
title_full_unstemmed Loss of Panx1 Impairs Mammary Gland Development at Lactation: Implications for Breast Tumorigenesis
title_short Loss of Panx1 Impairs Mammary Gland Development at Lactation: Implications for Breast Tumorigenesis
title_sort loss of panx1 impairs mammary gland development at lactation: implications for breast tumorigenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839729/
https://www.ncbi.nlm.nih.gov/pubmed/27099931
http://dx.doi.org/10.1371/journal.pone.0154162
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