G-Protein-Coupled Receptors in Adult Neurogenesis

被引:58
作者
Doze, Van A. [2 ]
Perez, Dianne M. [1 ]
机构
[1] Cleveland Clin Fdn, Lerner Res Inst, Dept Mol Cardiol, Cleveland, OH 44195 USA
[2] Univ N Dakota, Sch Med & Hlth Sci, Dept Pharmacol Physiol & Therapeut, Grand Forks, ND 58201 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
NEURAL STEM-CELLS; CYCLASE-ACTIVATING POLYPEPTIDE; METABOTROPIC GLUTAMATE RECEPTORS; CENTRAL-NERVOUS-SYSTEM; RAT CHOROID-PLEXUS; MOUSE SUBVENTRICULAR ZONE; HIPPOCAMPAL DENTATE GYRUS; NEWLY GENERATED NEURONS; TRAUMATIC BRAIN-INJURY; NITRIC-OXIDE SYNTHASE;
D O I
10.1124/pr.111.004762
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The importance of adult neurogenesis has only recently been accepted, resulting in a completely new field of investigation within stem cell biology. The regulation and functional significance of adult neurogenesis is currently an area of highly active research. G-protein-coupled receptors (GPCRs) have emerged as potential modulators of adult neurogenesis. GPCRs represent a class of proteins with significant clinical importance, because approximately 30% of all modern therapeutic treatments target these receptors. GPCRs bind to a large class of neurotransmitters and neuromodulators such as norepinephrine, dopamine, and serotonin. Besides their typical role in cellular communication, GPCRs are expressed on adult neural stem cells and their progenitors that relay specific signals to regulate the neurogenic process. This review summarizes the field of adult neurogenesis and its methods and specifies the roles of various GPCRs and their signal transduction pathways that are involved in the regulation of adult neural stem cells and their progenitors. Current evidence supporting adult neurogenesis as a model for self-repair in neuropathologic conditions, adult neural stem cell therapeutic strategies, and potential avenues for GPCR-based therapeutics are also discussed.
引用
收藏
页码:645 / 675
页数:31
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