Differential requirement of GRP94 and GRP78 in mammary gland development

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作者
Genyuan Zhu
Miao Wang
Benjamin Spike
Peter C. Gray
Jieli Shen
Sung-Hyung Lee
Si-Yi Chen
Amy S. Lee
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[1] University of Southern California,Department of Biochemistry and Molecular Biology
[2] Keck School of Medicine,Gene Expression Laboratories
[3] USC Norris Comprehensive Cancer Center,Clayton Foundation Laboratories for Peptide Biology
[4] The Salk Institute for Biological Studies,Department of Molecular Microbiology and Immunology
[5] The Salk Institute for Biological Studies,Hamon Center for Therapeutic Oncology Research, Departments of Surgery and Pharmacology
[6] University of Southern California,undefined
[7] Keck School of Medicine,undefined
[8] University of Texas Southwestern Medical Center,undefined
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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, Grp94f/f mammary glands, despite GRP94 deficiency, exhibited normal proliferation and ductal morphogenesis. Interestingly, MMTV-Cre, Grp78f/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 Grp78f/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.
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