首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Stromal cell-derived factor-1 (chemokine C-X-C motif ligand 12) and chemokine C-X-C motif receptor 4 are required for migration of gonadotropin-releasing hormone neurons to the forebrain.
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Stromal cell-derived factor-1 (chemokine C-X-C motif ligand 12) and chemokine C-X-C motif receptor 4 are required for migration of gonadotropin-releasing hormone neurons to the forebrain.

机译:促性腺激素释放激素神经元向前脑的迁移需要基质细胞衍生因子-1(趋化因子C-X-C基序配体12)和趋化因子C-X-C基序受体4。

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摘要

Gonadotropin-releasing hormone (GnRH) neurons migrate from the vomeronasal organ (VNO) in the nasal compartment to the basal forebrain in mice, beginning on embryonic day 11 (E11). These neurons use vomeronasal axons as guides to migrate through the nasal mesenchyme. Most GnRH neurons then migrate along the caudal branch of the vomeronasal nerve to reach the hypothalamus. We show here that stromal cell-derived factor-1 [SDF-1, also known as chemokine C-X-C motif ligand 12 (CXCL12)] is expressed in the embryonic nasal mesenchyme from as early as E10 in an increasing rostral to caudal gradient that is most intense at the border of the nasal mesenchyme and the telencephalon. Chemokine C-X-C motif receptor 4 (CXCR4), the receptor for SDF-1, is expressed by neurons in the olfactory epithelium and VNO. Cells derived from these sensory epithelia, including migrating GnRH neurons and ensheathing glial precursors of the migrating mass (MM), also express CXCR4, suggesting that they may use SDF-1 as a chemokine. In support of this, most GnRH neurons of CXCR4-/- mice fail to exit the VNO at E13, and comparatively few GnRH neurons reach the forebrain. There is also a significant decrease in the total number of GnRH neurons in CXCR4-/- mice and an increase in cell death within the VNO relative to controls. The MM is smaller in CXCR4-/- mice, suggesting that some MM cells also require SDF-1/CXCR4 function for migration and survival.
机译:从胚胎的第11天(E11)开始,促性腺激素释放激素(GnRH)神经元从小鼠鼻腔中的犁鼻器官(VNO)迁移至基底前脑。这些神经元使用犁鼻鼻轴突作为通过鼻间充质迁移的向导。然后,大多数GnRH神经元沿着犁鼻神经的尾支迁移,到达下丘脑。我们在这里显示,基质细胞衍生因子-1 [SDF-1,也称为趋化因子CXC基序配体12(CXCL12)]早在E10时就在胚胎鼻间充质中表达,其鼻翼到尾端的梯度逐渐增加在鼻间质和端脑的边界处强烈。 SDF-1受体趋化因子C-X-C基序受体4(CXCR4)由嗅觉上皮细胞和VNO中的神经元表达。从这些感觉上皮细胞衍生的细胞,包括正在迁移的GnRH神经元和正在迁移的团块(MM)的外皮神经胶质前体,也表达CXCR4,这表明它们可以使用SDF-1作为趋化因子。为此,大多数CXCR4-/-小鼠的GnRH神经元无法在E13处退出VNO,相对较少的GnRH神经元到达前脑。与对照相比,CXCR4-/-小鼠中GnRH神经元的总数也明显减少,而VNO内的细胞死亡增加。 CXCR4-/-小鼠中的MM较小,表明某些MM细胞还需要SDF-1 / CXCR4功能才能迁移和存活。

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