SDF and GABA interact to regulate axophilic migration of GnRH neurons

被引:44
作者
Casoni, Filippo [1 ]
Hutchins, B. Ian [1 ]
Donohue, Duncan [1 ]
Fornaro, Michele [1 ,2 ]
Condie, Brian G. [3 ]
Wray, Susan [1 ]
机构
[1] NINDS, Cellular & Dev Neurobiol Sect, NIH, Bethesda, MD 20892 USA
[2] Midwestern Univ, Dept Anat, Downers Grove, IL 60515 USA
[3] Univ Georgia, Dept Genet, Athens, GA 30602 USA
基金
美国国家卫生研究院;
关键词
GABA; GIRK; GnRH; Motility; Neuronal migration; SDF; HORMONE-RELEASING HORMONE; CELL-DERIVED FACTOR-1-ALPHA; GAMMA-AMINOBUTYRIC-ACID; LHRH NEURONS; INTERNEURON MIGRATION; OLFACTORY EXPLANTS; KALLMANN-SYNDROME; CEREBRAL-CORTEX; KNOCKOUT MICE; CLEFT-PALATE;
D O I
10.1242/jcs.101675
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Stromal derived growth factor (SDF-1) and gamma-aminobutyric acid (GABA) are two extracellular cues that regulate the rate of neuronal migration during development and may act synergistically. The molecular mechanisms of this interaction are still unclear. Gonadotropin releasing hormone-1 (GnRH) neurons are essential for vertebrate reproduction. During development, these neurons emerge from the nasal placode and migrate through the cribriform plate into the brain. Both SDF-1 and GABA have been shown to regulate the rate of GnRH neuronal migration by accelerating and slowing migration, respectively. As such, this system was used to explore the mechanism by which these molecules act to produce coordinated cell movement during development. In the present study, GABA and SDF-1 are shown to exert opposite effects on the speed of cell movement by activating depolarizing or hyperpolarizing signaling pathways, GABA via changes in chloride and SDF-1 via changes in potassium. GABA and SDF-1 were also found to act synergistically to promote linear rather than random movement. The simultaneous activation of these signaling pathways, therefore, results in tight control of cellular speed and improved directionality along the migratory pathway of GnRH neurons.
引用
收藏
页码:5015 / 5025
页数:11
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