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Expression of the mRNA stability regulator Tristetraprolin is required for lactation maintenance in the mouse mammary gland
Tristetraprolin (TTP), an mRNA-binding protein that negatively controls levels of inflammatory factors, is highly expressed in the lactating mouse mammary gland. To determine the biological relevance of this expression profile, we developed bi-transgenic mice in which this protein is specifically do...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5823555/ https://www.ncbi.nlm.nih.gov/pubmed/29492194 http://dx.doi.org/10.18632/oncotarget.23904 |
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author | Goddio, María Victoria Gattelli, Albana Tocci, Johanna M. Cuervo, Lourdes Pérez Stedile, Micaela Stumpo, Deborah J. Hynes, Nancy E. Blackshear, Perry J. Meiss, Roberto P. Kordon, Edith C. |
author_facet | Goddio, María Victoria Gattelli, Albana Tocci, Johanna M. Cuervo, Lourdes Pérez Stedile, Micaela Stumpo, Deborah J. Hynes, Nancy E. Blackshear, Perry J. Meiss, Roberto P. Kordon, Edith C. |
author_sort | Goddio, María Victoria |
collection | PubMed |
description | Tristetraprolin (TTP), an mRNA-binding protein that negatively controls levels of inflammatory factors, is highly expressed in the lactating mouse mammary gland. To determine the biological relevance of this expression profile, we developed bi-transgenic mice in which this protein is specifically down-regulated in the secretory mammary epithelium in the secretory mammary epithelium during lactation. Our data show that TTP conditional KO mice produced underweight litters, possibly due to massive mammary cell death induced during lactation without the requirement of additional stimuli. This effect was linked to overexpression of inflammatory cytokines, activation of STAT3 and down-regulation of AKT phosphorylation. Importantly, blocking TNFα activity in the lactating conditional TTP KO mice inhibited cell death and similar effects were observed when this treatment was applied to wild-type animals during 48 h after weaning. Therefore, our results demonstrate that during lactation TTP wards off early involution by preventing the increase of local inflammatory factors. In addition, our data reveal the relevance of locally secreted TNFα for triggering programmed cell death after weaning. |
format | Online Article Text |
id | pubmed-5823555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-58235552018-02-28 Expression of the mRNA stability regulator Tristetraprolin is required for lactation maintenance in the mouse mammary gland Goddio, María Victoria Gattelli, Albana Tocci, Johanna M. Cuervo, Lourdes Pérez Stedile, Micaela Stumpo, Deborah J. Hynes, Nancy E. Blackshear, Perry J. Meiss, Roberto P. Kordon, Edith C. Oncotarget Research Paper: Autophagy and Cell Death Tristetraprolin (TTP), an mRNA-binding protein that negatively controls levels of inflammatory factors, is highly expressed in the lactating mouse mammary gland. To determine the biological relevance of this expression profile, we developed bi-transgenic mice in which this protein is specifically down-regulated in the secretory mammary epithelium in the secretory mammary epithelium during lactation. Our data show that TTP conditional KO mice produced underweight litters, possibly due to massive mammary cell death induced during lactation without the requirement of additional stimuli. This effect was linked to overexpression of inflammatory cytokines, activation of STAT3 and down-regulation of AKT phosphorylation. Importantly, blocking TNFα activity in the lactating conditional TTP KO mice inhibited cell death and similar effects were observed when this treatment was applied to wild-type animals during 48 h after weaning. Therefore, our results demonstrate that during lactation TTP wards off early involution by preventing the increase of local inflammatory factors. In addition, our data reveal the relevance of locally secreted TNFα for triggering programmed cell death after weaning. Impact Journals LLC 2018-01-03 /pmc/articles/PMC5823555/ /pubmed/29492194 http://dx.doi.org/10.18632/oncotarget.23904 Text en Copyright: © 2018 Goddio et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper: Autophagy and Cell Death Goddio, María Victoria Gattelli, Albana Tocci, Johanna M. Cuervo, Lourdes Pérez Stedile, Micaela Stumpo, Deborah J. Hynes, Nancy E. Blackshear, Perry J. Meiss, Roberto P. Kordon, Edith C. Expression of the mRNA stability regulator Tristetraprolin is required for lactation maintenance in the mouse mammary gland |
title | Expression of the mRNA stability regulator Tristetraprolin is required for lactation maintenance in the mouse mammary gland |
title_full | Expression of the mRNA stability regulator Tristetraprolin is required for lactation maintenance in the mouse mammary gland |
title_fullStr | Expression of the mRNA stability regulator Tristetraprolin is required for lactation maintenance in the mouse mammary gland |
title_full_unstemmed | Expression of the mRNA stability regulator Tristetraprolin is required for lactation maintenance in the mouse mammary gland |
title_short | Expression of the mRNA stability regulator Tristetraprolin is required for lactation maintenance in the mouse mammary gland |
title_sort | expression of the mrna stability regulator tristetraprolin is required for lactation maintenance in the mouse mammary gland |
topic | Research Paper: Autophagy and Cell Death |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5823555/ https://www.ncbi.nlm.nih.gov/pubmed/29492194 http://dx.doi.org/10.18632/oncotarget.23904 |
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