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首页> 外文期刊>The Journal of Comparative Neurology >Developmental regulation of neuron-specific P2X(3) receptor expression in the rat cochlea.
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Developmental regulation of neuron-specific P2X(3) receptor expression in the rat cochlea.

机译:在大鼠耳蜗神经元特异性P2X(3)受体表达的发育调节。

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摘要

ATP-gated ion channels assembled from P2X(3) receptor (P2X(3)R) subunits contribute to neurotransmission and neurotrophic signaling, associated with neurite development and synaptogenesis, particularly in peripheral sensory neurons. Here, P2X(3)R expression was characterized in the rat cochlea from embryonic day 16 (E16) to adult (P49-56), using RT-PCR and immunohistochemistry. P2X(3)R mRNA was strongly expressed in the cochlea prior to birth, declined to a minimal level at P14, and was absent in adult tissue. P2X(3)R protein expression was confined to spiral ganglion neurons (SGN) within Rosenthal's canal of the cochlea. At E16, immunolabeling was detected in the SGN neurites, but not the distal neurite projection within the developing sensory epithelium (greater epithelial ridge). From E18, the immunolabeling was observed in the peripheral neurites innervating the inner hair cells but was reduced by P6. However, from P2-8, immunolabeling of the SGN neurites extended to include the outer spiral bundlefiber tract beneath the outer hair cells. This labeling of type II SGN afferent fiber declined after P8. By P14, all synaptic terminal immunolabeling in the organ of Corti was absent, and SGN cell body labeling was minimal. In adult cochlear tissue, P2X(3)R immunolabeling was not detected. Noise exposure did not induce P2X(3)R expression in the adult cochlea. These data indicate that ATP-gated ion channels incorporating P2X(3)R subunit expression are specifically targeted to the afferent terminals just prior to the onset of hearing, and likely contribute to the neurotrophic signaling which establishes functional auditory neurotransmission. J. Comp. Neurol. 484:133-143, 2005. (c) 2005 Wiley-Liss, Inc.
机译:由P2X(3)受体(P2X(3)R)亚基组装的ATP门控离子通道有助于神经传递和神经营养信号传导,与神经突发育和突触形成有关,特别是在周围感觉神经元中。在这里,P2X(3)R表达的特点是从胚胎第16天(E16)到成年(P49-56)的大鼠耳蜗,使用RT-PCR和免疫组织化学。 P2X(3)R mRNA在出生前在耳蜗中强烈表达,在P14处降至最低水平,并且在成人组织中不存在。 P2X(3)R蛋白表达仅限于耳蜗罗森塔尔管内的螺旋神经节神经元(SGN)。在E16时,在SGN神经突中检测到免疫标记,但在发育的感觉上皮(较大的上皮)内未检测到远端神经突突起。从E18开始,免疫标记在支配内部毛细胞的周围神经突中被P6还原。然而,从P2-8开始,SGN神经突的免疫标记扩展到包括在外部毛细胞下方的外部螺旋束纤维束。 P8后,II型SGN传入纤维的标签下降。通过P14,Corti器官中所有的突触末端免疫标记都不存在,并且SGN细胞体标记极少。在成人的人工耳蜗组织中,未检测到P2X(3)R免疫标记。噪声暴露不会在成人耳蜗中诱导P2X(3)R表达。这些数据表明,结合P2X(3)R亚基表达的ATP门控离子通道正好在听力发作之前专门针对传入的末端,并且可能有助于建立功能性听觉神经传递的神经营养信号传导。 J.比较神经元。 484:133-143,2005.(c)2005 Wiley-Liss,Inc.

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