Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/53943
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Type: Journal article
Title: Nedd4 controls animal growth by regulating IGF-1 signaling
Author: Cao, X.
Lill, N.
Boase, N.
Shi, P.
Croucher, D.
Shan, H.
Qu, J.
Sweezer, E.
Place, T.
Kirby, P.
Daly, R.
Kumar, S.
Yang, B.
Citation: Science Signaling, 2008; 1(38):1-10
Publisher: American Assoc Advancement Science
Issue Date: 2008
ISSN: 1945-0877
1937-9145
Statement of
Responsibility: 
Xiao R. Cao, Nancy L. Lill, Natasha Boase, Peijun P. Shi, David R. Croucher, Hongbo Shan, Jing Qu, Eileen M. Sweezer, Trenton Place, Patricia A. Kirby, Roger J. Daly, Sharad Kumar, and Baoli Yang
Abstract: The ubiquitin ligase Nedd4 has been proposed to regulate a number of signaling pathways, but its physiological role in mammals has not been characterized. Here we present an analysis of Nedd4-null mice to show that loss of Nedd4 results in reduced insulin-like growth factor 1 (IGF-1) and insulin signaling, delayed embryonic development, reduced growth and body weight, and neonatal lethality. In mouse embryonic fibroblasts, mitogenic activity was reduced, the abundance of the adaptor protein Grb10 was increased, and the IGF-1 receptor, which is normally present on the plasma membrane, was mislocalized. However, surface expression of IGF-1 receptor was restored in homozygous mutant mouse embryonic fibroblasts after knockdown of Grb10, and Nedd4–/– lethality was rescued by maternal inheritance of a disrupted Grb10 allele. Thus, in vivo, Nedd4 appears to positively control IGF-1 and insulin signaling partly through the regulation of Grb10 function.
Keywords: Cells, Cultured
Cell Membrane
Animals
Mice
Mice, Mutant Strains
Insulin
Ubiquitin-Protein Ligases
Receptor, IGF Type 1
Insulin-Like Growth Factor I
Signal Transduction
Phosphorylation
GRB10 Adaptor Protein
Endosomal Sorting Complexes Required for Transport
Nedd4 Ubiquitin Protein Ligases
DOI: 10.1126/scisignal.1160940
Appears in Collections:Aurora harvest 5
Medicine publications

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