Karlsson M, Clary D O, Lefcort F B, Reichardt L F, Karten H J, Hallböök F
Uppsala University, Sweden.
J Comp Neurol. 1998 Oct 26;400(3):408-16.
Nerve growth factor is known to stimulate neurite outgrowth and support neuronal survival during embryonic development. We have studied the expression of the nerve growth factor receptor, TrkA, at both mRNA and protein levels during the course of chicken retinal development. Furthermore, we have compared the expression of trkA mRNA with that of the 75-kD low-affinity neurotrophin receptor (p75NTR). RNase protection assay identified peak-levels of trkA mRNA in the late embryonic retina. Using in situ hybridization and immunohistochemistry, we found cells expressing TrkA in both the internal and the external part of the inner nuclear layer, corresponding to amacrine and horizontal cells, respectively. The TrkA-expressing amacrine cell has a unistratified dendritic arborization in the second sublamina of the inner plexiform layer, and may represent the stellate amacrine cell described by Cajal. The horizontal cells, possessing arciform dendrite processes in the outer plexiform layer, showed strong TrkA immunoreactivity in both dendrites and cell bodies. During the course of retinal development, the TrkA-expressing amacrine cells decreased in number, whereas the TrkA-expressing horizontal cells persisted. Because nerve growth factor was expressed where the horizontal cells, but not where the amacrine cells were located, these findings raise the question of whether nerve growth factor could locally support the survival of TrkA-expressing interneurons during retinal development.
已知神经生长因子在胚胎发育过程中可刺激神经突生长并支持神经元存活。我们研究了鸡视网膜发育过程中神经生长因子受体TrkA在mRNA和蛋白质水平的表达。此外,我们还比较了trkA mRNA与75-kD低亲和力神经营养因子受体(p75NTR)的表达。核糖核酸酶保护试验确定了胚胎晚期视网膜中trkA mRNA的峰值水平。通过原位杂交和免疫组织化学,我们发现内核层内部和外部均有表达TrkA的细胞,分别对应无长突细胞和水平细胞。表达TrkA的无长突细胞在内网状层的第二个亚层中具有单层树突分支,可能代表了 Cajal 描述的星状无长突细胞。水平细胞在外网状层中具有弓形树突突起,其树突和细胞体均显示出强烈的TrkA免疫反应性。在视网膜发育过程中,表达TrkA的无长突细胞数量减少,而表达TrkA的水平细胞持续存在。由于神经生长因子在水平细胞所在部位表达,而不在无长突细胞所在部位表达,这些发现提出了一个问题,即神经生长因子是否能在视网膜发育过程中局部支持表达TrkA的中间神经元的存活。