Department of Physiology, University of Kentucky, Lexington, Kentucky 40536-0298, USA.
J Neurosci Res. 2010 Nov 15;88(15):3243-56. doi: 10.1002/jnr.22497.
Neurogenesis of projection neurons requires that axons be initiated, extended, and connected. Differences in the expression of axon growth and guidance genes must drive these events, but comprehensively characterizing these differences in a single neuronal type has not been accomplished. Guided by a catalog of gene expression in olfactory sensory neurons (OSNs), in situ hybridization and immunohistochemistry revealed that Cxcr4 and Dbn1, two axon initiation genes, marked the developmental transition from basal progenitor cells to immature OSNs in the olfactory epithelium. The CXCR4 immunoreactivity of these nascent OSNs overlapped partially with markers of proliferation of basal progenitor cells and partially with immunoreactivity for GAP43, the canonical marker of immature OSNs. Intracellular guidance cue signaling transcripts Ablim1, Crmp1, Dypsl2, Dpysl3, Dpysl5, Gap43, Marcskl1, and Stmn1-4 were specific to, or much more abundant in, the immature OSN layer. Receptors that mediate axonal inhibition or repulsion tended to be expressed in both immature and mature OSNs (Plxna1, Plxna4, Nrp2, Efna5) or specifically in mature OSNs (Plxna3, Unc5b, Efna3, Epha5, Epha7), although some were specific to immature OSNs (Plxnb1, Plxnb2, Plxdc2, Nrp1). Cell adhesion molecules were expressed either by both immature and mature OSNs (Dscam, Ncam1, Ncam2, Nrxn1) or solely by immature OSNs (Chl1, Nfasc1, Dscaml1). Given the loss of intracellular signaling protein expression, the continued expression of guidance cue receptors in mature OSNs is consistent with a change in the role of these receptors, perhaps to sending signals back to the cell body and nucleus.
投射神经元的神经发生要求轴突起始、延伸和连接。轴突生长和导向基因的表达差异必然驱动这些事件,但在单一神经元类型中全面描述这些差异尚未完成。在嗅感觉神经元(OSN)基因表达目录的指导下,原位杂交和免疫组织化学显示,两个轴突起始基因 Cxcr4 和 Dbn1 标记了嗅上皮中从基底祖细胞到不成熟 OSN 的发育转变。这些新生 OSN 的 CXCR4 免疫反应性部分与基底祖细胞增殖的标志物重叠,部分与不成熟 OSN 的经典标志物 GAP43 的免疫反应性重叠。细胞内导向信号转导转录物 Ablim1、Crmp1、Dypsl2、Dpysl3、Dpysl5、Gap43、Marcskl1 和 Stmn1-4 特异性存在于或在不成熟 OSN 层中更丰富。介导轴突抑制或排斥的受体倾向于在不成熟和成熟 OSN 中表达(Plxna1、Plxna4、Nrp2、Efna5)或特异性在成熟 OSN 中表达(Plxna3、Unc5b、Efna3、Epha5、Epha7),尽管有些受体特异性存在于不成熟 OSN 中(Plxnb1、Plxnb2、Plxdc2、Nrp1)。细胞粘附分子由不成熟和成熟 OSN 共同表达(Dscam、Ncam1、Ncam2、Nrxn1)或仅由不成熟 OSN 表达(Chl1、Nfasc1、Dscaml1)。考虑到细胞内信号转导蛋白表达的丧失,成熟 OSN 中导向 cue 受体的持续表达与其受体作用的改变一致,可能是将信号发送回细胞体和核。