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Differential requirement of GRP94 and GRP78 in mammary gland development
Glucose Regulated Protein (GRP) 94 and GRP78 are critical molecular chaperones and regulators of signaling. Conditional knockout mouse models have revealed tissue specific requirements for GRP94 and GRP78, including selection for allele retention in specific cell types. Here we report the consequenc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066247/ https://www.ncbi.nlm.nih.gov/pubmed/24953136 http://dx.doi.org/10.1038/srep05390 |
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author | Zhu, Genyuan Wang, Miao Spike, Benjamin Gray, Peter C. Shen, Jieli Lee, Sung-Hyung Chen, Si-Yi Lee, Amy S. |
author_facet | Zhu, Genyuan Wang, Miao Spike, Benjamin Gray, Peter C. Shen, Jieli Lee, Sung-Hyung Chen, Si-Yi Lee, Amy S. |
author_sort | Zhu, Genyuan |
collection | PubMed |
description | Glucose Regulated Protein (GRP) 94 and GRP78 are critical molecular chaperones and regulators of signaling. Conditional knockout mouse models have revealed tissue specific requirements for GRP94 and GRP78, including selection for allele retention in specific cell types. Here we report the consequences of mammary-targeted knockout of these GRPs. Our studies revealed that MMTV-Cre, Grp94(f/f) mammary glands, despite GRP94 deficiency, exhibited normal proliferation and ductal morphogenesis. Interestingly, MMTV-Cre, Grp78(f/f) mammary glands displayed only slightly reduced GRP78 protein levels, associating with the retention of the non-recombined Grp78 floxed alleles in isolated mammary epithelial cells and displayed phenotypes comparable to wild-type glands. In contrast, transduction of isolated Grp78(f/f) mammary epithelial stem/progenitor cells with adenovirus expressing GFP and Cre-recombinase was successful in GRP78 ablation, and the GFP sorted cells failed to give rise to repopulated mammary glands in de-epithelialized recipient mice. These studies imply GRP78, but not GRP94, is required for mammary gland development. |
format | Online Article Text |
id | pubmed-4066247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40662472014-06-23 Differential requirement of GRP94 and GRP78 in mammary gland development Zhu, Genyuan Wang, Miao Spike, Benjamin Gray, Peter C. Shen, Jieli Lee, Sung-Hyung Chen, Si-Yi Lee, Amy S. Sci Rep Article Glucose Regulated Protein (GRP) 94 and GRP78 are critical molecular chaperones and regulators of signaling. Conditional knockout mouse models have revealed tissue specific requirements for GRP94 and GRP78, including selection for allele retention in specific cell types. Here we report the consequences of mammary-targeted knockout of these GRPs. Our studies revealed that MMTV-Cre, Grp94(f/f) mammary glands, despite GRP94 deficiency, exhibited normal proliferation and ductal morphogenesis. Interestingly, MMTV-Cre, Grp78(f/f) mammary glands displayed only slightly reduced GRP78 protein levels, associating with the retention of the non-recombined Grp78 floxed alleles in isolated mammary epithelial cells and displayed phenotypes comparable to wild-type glands. In contrast, transduction of isolated Grp78(f/f) mammary epithelial stem/progenitor cells with adenovirus expressing GFP and Cre-recombinase was successful in GRP78 ablation, and the GFP sorted cells failed to give rise to repopulated mammary glands in de-epithelialized recipient mice. These studies imply GRP78, but not GRP94, is required for mammary gland development. Nature Publishing Group 2014-06-23 /pmc/articles/PMC4066247/ /pubmed/24953136 http://dx.doi.org/10.1038/srep05390 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Zhu, Genyuan Wang, Miao Spike, Benjamin Gray, Peter C. Shen, Jieli Lee, Sung-Hyung Chen, Si-Yi Lee, Amy S. Differential requirement of GRP94 and GRP78 in mammary gland development |
title | Differential requirement of GRP94 and GRP78 in mammary gland development |
title_full | Differential requirement of GRP94 and GRP78 in mammary gland development |
title_fullStr | Differential requirement of GRP94 and GRP78 in mammary gland development |
title_full_unstemmed | Differential requirement of GRP94 and GRP78 in mammary gland development |
title_short | Differential requirement of GRP94 and GRP78 in mammary gland development |
title_sort | differential requirement of grp94 and grp78 in mammary gland development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066247/ https://www.ncbi.nlm.nih.gov/pubmed/24953136 http://dx.doi.org/10.1038/srep05390 |
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