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腺苷A2A受体通过调节神经元极化和轴突形成,对皮质投射神经元的放射状迁移起作用。

Adenosine A2A Receptors Contribute to the Radial Migration of Cortical Projection Neurons through the Regulation of Neuronal Polarization and Axon Formation.

作者信息

Alçada-Morais Sofia, Gonçalves Nélio, Moreno-Juan Verónica, Andres Belén, Ferreira Sofia, Marques Joana M, Magalhães Joana, Rocha João M M, Xu Xinli, Partidário Matilde, Cunha Rodrigo A, López-Bendito Guillermina, Rodrigues Ricardo J

机构信息

CNC-Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra 3004-504, Portugal.

Institute for Interdisciplinary Research, University of Coimbra, Coimbra 3030-789, Portugal.

出版信息

Cereb Cortex. 2021 Oct 22;31(12):5652-5663. doi: 10.1093/cercor/bhab188.

DOI:10.1093/cercor/bhab188
PMID:34184030
Abstract

Cortical interneurons born in the subpallium reach the cortex through tangential migration, whereas pyramidal cells reach their final position by radial migration. Purinergic signaling via P2Y1 receptors controls the migration of intermediate precursor cells from the ventricular zone to the subventricular zone. It was also reported that the blockade of A2A receptors (A2AR) controls the tangential migration of somatostatin+ interneurons. Here we found that A2AR control radial migration of cortical projection neurons. In A2AR-knockout (KO) mouse embryos or naïve mouse embryos exposed to an A2AR antagonist, we observed an accumulation of early-born migrating neurons in the lower intermediate zone at late embryogenesis. In utero knockdown of A2AR also caused an accumulation of neurons at the lower intermediate zone before birth. This entails the presently identified ability of A2AR to promote multipolar-bipolar transition and axon formation, critical for the transition of migrating neurons from the intermediate zone to the cortical plate. This effect seems to require extracellular ATP-derived adenosine since a similar accumulation of neurons at the lower intermediate zone was observed in mice lacking ecto-5'-nucleotidase (CD73-KO). These findings frame adenosine as a fine-tune regulator of the wiring of cortical inhibitory and excitatory networks.

摘要

起源于皮质下的皮质中间神经元通过切向迁移到达皮质,而锥体细胞则通过径向迁移到达其最终位置。经由P2Y1受体的嘌呤能信号传导控制中间前体细胞从脑室区向室下区的迁移。也有报道称,A2A受体(A2AR)的阻断控制生长抑素阳性中间神经元的切向迁移。在此,我们发现A2AR控制皮质投射神经元的径向迁移。在A2AR基因敲除(KO)小鼠胚胎或暴露于A2AR拮抗剂的新生小鼠胚胎中,我们观察到在胚胎发育后期,早期迁移的神经元在下部中间区积聚。在子宫内敲低A2AR也会导致出生前神经元在下部中间区积聚。这意味着目前已确定的A2AR促进多极-双极转变和轴突形成的能力,这对于迁移神经元从中间区向皮质板的转变至关重要。这种效应似乎需要细胞外ATP衍生的腺苷,因为在缺乏胞外5'-核苷酸酶(CD73-KO)的小鼠中,在下部中间区也观察到类似的神经元积聚。这些发现将腺苷界定为皮质抑制和兴奋性网络布线的微调调节器。

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