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CXCR7 Receptor Controls the Maintenance of Subpial Positioning of Cajal-Retzius Cells

机译:CXCR7受体控制Cajal-Retzius细胞在椎弓根下定位的维持

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摘要

Cajal-Retzius (CR) cells are essential for cortical development and lamination. These pioneer neurons arise from distinct progenitor sources, including the cortical hem and the ventral pallium at pallium-subpallium boundary (PSB). CXCR4, the canonical receptor for the chemokine CXCL12, controls the superficial location of hem-derived CR cells. However, recent studies showed that CXCR7, a second CXCL12 receptor, is also expressed in CR cells at early developmental stages. We thus investigated the role of CXCR7 during CR cell development using multiple loss-of-function approaches. Cxcr7 gene inactivation led to aberrant localization of Reelin-positive cells within the pallium. In addition, Cxcr7(-/-) mice were characterized by significant accumulation of ectopic CR cells in the lateral part of the dorsal pallium compared with Cxcr4 knockout mice. Loss-of-function approaches, using either gene targeting or pharmacological receptor inhibition, reveal that CXCR7 and CXCR4 act both in CR positioning. Finally, conditional Cxcr7 deletion in cells derived from Dbx1-expressing progenitors indicates an essential role of CXCR7 in controlling the positioning of a subpopulation of PSB-derived CR cells. Our data demonstrate that CXCR7 has a role in the positioning of hem and PSB-derived CR cells, CXCL12 regulating CR cell subpial localization through the combined action of CXCR4 and CXCR7.
机译:Cajal-Retzius(CR)细胞对于皮层发育和层压至关重要。这些先驱神经元来自不同的祖细胞,包括皮质下摆和位于皮下-皮层下边界(PSB)的腹侧皮层。 CXCR4是趋化因子CXCL12的规范受体,它控制下摆来源的CR细胞的表面位置。但是,最近的研究表明,第二种CXCL12受体CXCR7在早期发育阶段也在CR细胞中表达。因此,我们使用多种功能丧失方法研究了CXCR7在CR细胞发育过程中的作用。 Cxcr7基因失活导致大脑皮层内Reelin阳性细胞异常定位。此外,与Cxcr4基因敲除小鼠相比,Cxcr7(-/-)小鼠的特征在于异位CR细胞大量积聚在背颅骨外侧。使用基因靶向或药理学受体抑制的功能丧失方法显示,CXCR7和CXCR4均在CR定位中起作用。最后,从表达Dbx1的祖细胞衍生的细胞中有条件的Cxcr7缺失表明CXCR7在控制PSB衍生的CR细胞亚群的定位中的重要作用。我们的数据表明,CXCR7在下摆和PSB衍生的CR细胞的定位中具有作用,CXCL12通过CXCR4和CXCR7的联合作用来调节CR细胞在椎管下的定位。

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