Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Genyuan, Wang, Miao, Spike, Benjamin, Gray, Peter C., Shen, Jieli, Lee, Sung-Hyung, Chen, Si-Yi, Lee, Amy S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
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
_version_ 1782322153836773376
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
work_keys_str_mv AT zhugenyuan differentialrequirementofgrp94andgrp78inmammaryglanddevelopment
AT wangmiao differentialrequirementofgrp94andgrp78inmammaryglanddevelopment
AT spikebenjamin differentialrequirementofgrp94andgrp78inmammaryglanddevelopment
AT graypeterc differentialrequirementofgrp94andgrp78inmammaryglanddevelopment
AT shenjieli differentialrequirementofgrp94andgrp78inmammaryglanddevelopment
AT leesunghyung differentialrequirementofgrp94andgrp78inmammaryglanddevelopment
AT chensiyi differentialrequirementofgrp94andgrp78inmammaryglanddevelopment
AT leeamys differentialrequirementofgrp94andgrp78inmammaryglanddevelopment