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本文引用的文献

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Culturing embryonic nasal explants for developmental and physiological study.培养胚胎鼻外植体用于发育和生理学研究。
Curr Protoc Neurosci. 2012 Apr;Chapter 3:Unit 3.25.1-16. doi: 10.1002/0471142301.ns0325s59.
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Development of novel CXCR4-based therapeutics.新型 CXCR4 靶向治疗药物的研发。
Expert Opin Investig Drugs. 2012 Mar;21(3):341-53. doi: 10.1517/13543784.2012.656197. Epub 2012 Jan 28.
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Laminin 511 partners with laminin 332 to mediate directional migration of Madin-Darby canine kidney epithelial cells.层粘连蛋白 511 与层粘连蛋白 332 结合,介导犬肾上皮细胞的定向迁移。
Mol Biol Cell. 2012 Jan;23(1):121-36. doi: 10.1091/mbc.E11-08-0718. Epub 2011 Oct 26.
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SDF1 regulates leading process branching and speed of migrating interneurons.SDF1 调节引导过程分支和迁移中间神经元的速度。
J Neurosci. 2011 Feb 2;31(5):1739-45. doi: 10.1523/JNEUROSCI.3118-10.2011.
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Cxcr7 controls neuronal migration by regulating chemokine responsiveness.Cxcr7 通过调节趋化因子的反应性来控制神经元迁移。
Neuron. 2011 Jan 13;69(1):77-90. doi: 10.1016/j.neuron.2010.12.006.
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CXCR4 and CXCR7 have distinct functions in regulating interneuron migration.CXCR4 和 CXCR7 在调节中间神经元迁移方面具有不同的功能。
Neuron. 2011 Jan 13;69(1):61-76. doi: 10.1016/j.neuron.2010.12.005.
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Expression and function of CXCR7 in the mouse forebrain.CXCR7 在小鼠前脑中的表达和功能。
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Neurexins physically and functionally interact with GABA(A) receptors.神经连接蛋白在物理和功能上与 GABA(A)受体相互作用。
Neuron. 2010 May 13;66(3):403-16. doi: 10.1016/j.neuron.2010.04.008.
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Emerging roles for G protein-gated inwardly rectifying potassium (GIRK) channels in health and disease.G 蛋白门控内向整流钾 (GIRK) 通道在健康和疾病中的新兴作用。
Nat Rev Neurosci. 2010 May;11(5):301-15. doi: 10.1038/nrn2834. Epub 2010 Apr 14.
10
Neuropeptide Y directly inhibits neuronal activity in a subpopulation of gonadotropin-releasing hormone-1 neurons via Y1 receptors.神经肽 Y 通过 Y1 受体直接抑制促性腺激素释放激素-1 神经元亚群的神经元活性。
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SDF 与 GABA 相互作用调节 GnRH 神经元的轴突迁移。

SDF and GABA interact to regulate axophilic migration of GnRH neurons.

机构信息

Cellular and Developmental Neurobiology Section, NINDS/NIH, Bethesda, MD 20892, USA.

出版信息

J Cell Sci. 2012 Nov 1;125(Pt 21):5015-25. doi: 10.1242/jcs.101675. Epub 2012 Sep 12.

DOI:10.1242/jcs.101675
PMID:22976302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3533389/
Abstract

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.

摘要

基质衍生生长因子 (SDF-1) 和γ-氨基丁酸 (GABA) 是两种调节发育过程中神经元迁移速度的细胞外信号,它们可能具有协同作用。这种相互作用的分子机制尚不清楚。促性腺激素释放激素-1 (GnRH) 神经元对脊椎动物的繁殖至关重要。在发育过程中,这些神经元从鼻基板中出现,并通过筛板迁移到大脑中。SDF-1 和 GABA 都被证明可以通过加速和减缓迁移来分别调节 GnRH 神经元迁移的速度。因此,该系统被用于探索这些分子如何通过产生协调的细胞运动来发挥作用的机制。在本研究中,GABA 和 SDF-1 通过激活去极化或超极化信号通路对细胞运动速度产生相反的影响,GABA 通过氯离子变化,SDF-1 通过钾离子变化。还发现 GABA 和 SDF-1 协同作用以促进线性而不是随机运动。因此,这些信号通路的同时激活导致对细胞速度的严格控制,并沿着 GnRH 神经元的迁移途径提高方向性。