Regulation of stem cell pluripotency and differentiation by G protein coupled receptors

被引:34
作者
Callihan, Phillip
Mumaw, Jennifer [2 ]
Machacek, David W. [3 ]
Stice, Steve L. [2 ,3 ]
Hooks, Shelley B. [1 ]
机构
[1] Univ Georgia, Coll Pharm, Dept Pharmaceut & Biomed Sci, Athens, GA 30602 USA
[2] Univ Georgia, Ctr Regenerat Biosci, Athens, GA 30602 USA
[3] Aruna Biomed, Athens, GA USA
关键词
G protein coupled receptor; GPCR; Pluripotency; Stem cell; Differentiation; CYCLASE-ACTIVATING POLYPEPTIDE; METABOTROPIC GLUTAMATE RECEPTORS; LEUKEMIA INHIBITORY FACTOR; MESENCHYMAL TRANSITION PROCESS; WNT SIGNALING PATHWAY; SELF-RENEWAL; LYSOPHOSPHATIDIC ACID; NEURONAL DIFFERENTIATION; NEURAL DIFFERENTIATION; IN-VITRO;
D O I
10.1016/j.pharmthera.2010.10.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Stem cell-based therapeutics have the potential to effectively treat many terminal and debilitating human diseases, but the mechanisms by which their growth and differentiation are regulated are incompletely defined. Recent data from multiple systems suggest major roles for G protein coupled receptor (GPCR) pathways in regulating stem cell function in vivo and in vitro. The goal of this review is to illustrate common ground between the growing field of stem cell therapeutics and the long-established field of G protein coupled receptor signaling. Herein, we briefly introduce basic stem cell biology and discuss how several conserved pathways regulate pluripotency and differentiation in mouse and human stem cells. We further discuss general mechanisms by which GPCR signaling may impact these pluripotency and differentiation pathways, and summarize specific examples of receptors from each of the major GPCR subfamilies that have been shown to regulate stem cell function. Finally, we discuss possible therapeutic implications of GPCR regulation of stem cell function. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:290 / 306
页数:17
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