The association of NHERF adaptor proteins with G protein-coupled receptors and receptor tyrosine kinases

被引:143
作者
Weinman, EJ [1 ]
Hall, RA
Friedman, PA
Liu-Chen, LY
Shenolikar, S
机构
[1] Univ Maryland, Sch Med, Dept Med, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA
[3] Dept Vet Affairs Med Ctr, Med Serv, Baltimore, MD 21201 USA
[4] Emory Univ, Sch Med, Rollins Res Ctr, Dept Pharmacol, Atlanta, GA 30322 USA
[5] Univ Pittsburgh, Sch Med, Dept Pharmacol, Pittsburgh, PA 15261 USA
[6] Univ Pittsburgh, Sch Med, Dept Med, Pittsburgh, PA 15261 USA
[7] Temple Univ, Sch Med, Dept Pharmacol, Philadelphia, PA 19140 USA
[8] Temple Univ, Sch Med, Ctr Subst Abuse Res, Philadelphia, PA 19140 USA
[9] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
关键词
PDZ adaptor proteins; multiple protein complexes; hormone receptors; growth factor receptors;
D O I
10.1146/annurev.physiol.68.040104.131050
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The sodium-hydrogen exchanger regulatory factors (NHERF-1 and NHERF-2) are a family of adaptor proteins characterized by the presence of two tandem PDZ protein interaction domains and a C-terminal domain that binds the cytoskeleton proteins ezrin, radixin, moesin,and merlin. The NHERF proteins are highly expressed in the kidney, small intestine, and other organs, where they associate with a number of transporters and ion channels, signaling proteins, and transcription factors. Recent evidence has revealed important associations between the NHERF proteins and several G protein-coupled receptors such as the beta(2)-adrenergic receptor, the kappa-Opioid receptor, and the parathyroid hormone receptor, as well as growth factor tyrosine kinase receptors Such as the platelet-derived growth factor receptor and the epidermal growth factor receptor. This review summarizes the emerging data of e biochemical mechanisms, physiologic Outcomes, and potential clinical implications of the assembly and disassembly of receptor/NHERF complexes.
引用
收藏
页码:491 / 505
页数:15
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