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在发育中的嗅觉系统中,神经元表面糖蛋白Thy-1的表达受转录后调控,并在空间上受到调节。

Expression of the neuronal surface glycoprotein Thy-1 is under post-transcriptional control, and is spatially regulated, in the developing olfactory system.

作者信息

Xue G P, Calvert R A, Morris R J

机构信息

Norman and Sadie Lee Research Centre, Laboratory of Neurobiology, National Institute for Medical Research, Mill Hill, London, UK.

出版信息

Development. 1990 Aug;109(4):851-64. doi: 10.1242/dev.109.4.851.

Abstract

Expression of the neuronal cell surface glycoprotein Thy-1 has been studied during the development of the olfactory bulb in mice and rats, using in situ hybridisation and immunohistochemistry to follow the appearance of Thy-1 mRNA and protein, respectively. The mRNA was first detected 4 days before birth on all mitral cells, the main projection neuron of the bulb, as they formed a distinct layer and grew dendrites. At no stage was any spatial gradient of expression of Thy-1 mRNA evident around the mitral cell layer. Thy-1 protein, on the other hand, was first detectable 2 days later on a group of mitral cells immediately adjacent the point of entry of the olfactory nerve. The numbers of immunoreactive cells spread, over the next 7 days, to include all mitral cells, those located rostrally and laterally in the bulb being slowest to express Thy-1 protein. Thus there was a spatiotemporal gradient of expression of Thy-1 protein, which was not apparent in the earlier general expression of its mRNA, suggesting that some further inductive signal was required after transcription in order to get effective production of protein. Analysis of the growth of the mitral cell axons in the lateral olfactory tract suggested this signal was related to the cessation of axonogenesis, as Thy-1 immunoreactivity became detectable on these axons only when their expression of the transient epitope detected by the G10 antibody, present on microtubule-associated protein (MAP)1x only during axonal growth, declined. For the first week after Thy-1 protein appeared on mitral cells, it was not distributed uniformally on their surface. Immunoreaction was relatively weak on the somatic surface, and the molecule appeared to be entirely excluded from the distal regions of its main dendrite, above the outer plexiform layer. Here the dendrite reaches up to the synaptic glomeruli formed with the incoming olfactory nerve axons. These distal regions of the dendritic shaft became immunoreactive only after the periglomerular cells had first begun to express Thy-1 protein in the glomeruli. Immunolabelling of the somatic membrane then increased, to give the adult pattern of uniform Thy-1 labelling of the neuronal membrane by the end of the second postnatal week. It is suggested that some of the molecular features of Thy-1, and anatomical features of the main bulb, could interact to produce this initial restriction of Thy-1 to particular parts of the mitral cell surface.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在小鼠和大鼠嗅球发育过程中,研究了神经元细胞表面糖蛋白Thy-1的表达情况,分别使用原位杂交和免疫组织化学方法追踪Thy-1 mRNA和蛋白质的出现。出生前4天,在嗅球的主要投射神经元——所有的二尖瓣细胞形成一个独特的层并长出树突时,首次检测到mRNA。在二尖瓣细胞层周围,Thy-1 mRNA的表达在任何阶段都没有明显的空间梯度。另一方面,Thy-1蛋白在2天后首次在紧邻嗅神经进入点的一组二尖瓣细胞中被检测到。在接下来的7天里,免疫反应阳性细胞的数量扩展到包括所有二尖瓣细胞,位于嗅球前部和外侧的细胞表达Thy-1蛋白的速度最慢。因此,Thy-1蛋白的表达存在时空梯度,这在其mRNA早期的普遍表达中并不明显,表明转录后需要一些进一步的诱导信号才能有效产生蛋白质。对二尖瓣细胞轴突在外侧嗅束中生长的分析表明,这个信号与轴突发生的停止有关,因为只有当轴突上与微管相关蛋白(MAP)1x结合的、仅在轴突生长期间存在的瞬时表位的表达下降时,Thy-1免疫反应性才在这些轴突上被检测到。在Thy-1蛋白出现在二尖瓣细胞上后的第一周,它在细胞表面的分布并不均匀。体细胞表面的免疫反应相对较弱,并且该分子似乎完全被排除在其主要树突的远端区域,即在外部丛状层上方。在这里,树突延伸到与传入的嗅神经轴突形成的突触小球。只有在小球周围的细胞首先开始在小球中表达Thy-1蛋白后,树突干的这些远端区域才会产生免疫反应。然后体细胞膜的免疫标记增加,在出生后第二周结束时形成成年期神经元膜上Thy-1均匀标记的模式。有人提出,Thy-1的一些分子特征和嗅球的解剖特征可能相互作用,导致Thy-1最初局限于二尖瓣细胞表面的特定部位。(摘要截短至400字)

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