King Carolyn, Lacey Richard, Rodger Jennifer, Bartlett Carole, Dunlop Sarah, Beazley Lyn
School of Animal Biology, The University of Western Australia, Nedlands 6907, Australia.
Exp Neurol. 2004 Jun;187(2):380-7. doi: 10.1016/j.expneurol.2004.02.006.
EphA receptors and their ligands the ephrin-As, expressed as retinal and tectal gradients, are required for the development of retino-tectal topography [Neuron 25 (2000) 563] and its restoration during goldfish optic nerve regeneration [Mol. Cell. Neurosci. 25 (2004) 56]. We have reported previously that, during regeneration, a transient EphA3/A5 gradient is formed by differential expression across the entire retinal ganglion cell (RGC) population [Neurosci. Abs. 33 (2003) 358.2; Exp. Neurol. 183 (2003) 593]. In retino-recipient tectal layers, ephrin-A2 is normally expressed by only a sub-population of cells, but during regeneration, there is a graded increase with more expressing cells caudally than rostrally [Exp. Neurol. 166 (2000) 196]. Here, we examine the characteristics of tectal ephrin-A2 expression during regeneration. We report that the level of ephrin-A2 expression is comparable for all ephrin-A2-positive cells in normal animals and during regeneration. Using double-labelling immunohistochemistry for ephrin-A2 and specific cell markers (NeuN for neurons, GA5 for astrocytes, NN-1 for microglia/endothelial cells and 6D2 for oligodendrocytes), we demonstrate that ephrin-A2-expressing cells, as in normal animals, are exclusively neuronal. Moreover, double labelling with BrdU showed that ephrin-A2 is expressed in resident cells and not those generated during optic nerve regeneration [Brain Res. 854 (2000) 178, 153 (1978) 345].
EphA受体及其配体ephrin - A,以视网膜和顶盖梯度形式表达,对视顶盖拓扑结构的发育[《神经元》25卷(2000年)563页]以及金鱼视神经再生过程中其拓扑结构的恢复[《分子与细胞神经科学》25卷(2004年)56页]是必需的。我们之前报道过,在再生过程中,通过整个视网膜神经节细胞(RGC)群体的差异表达形成了一个短暂的EphA3/A5梯度[《神经科学文摘》33卷(2003年)358.2;《实验神经病学》183卷(2003年)593页]。在视网膜接受区的顶盖层中,ephrin - A2通常仅由一部分细胞表达,但在再生过程中,表达细胞呈梯度增加,尾部比头部更多[《实验神经病学》166卷(2000年)196页]。在此,我们研究再生过程中顶盖ephrin - A2表达的特征。我们报道,在正常动物和再生过程中,所有ephrin - A2阳性细胞的ephrin - A2表达水平相当。利用针对ephrin - A2和特定细胞标志物(神经元用NeuN、星形胶质细胞用GA5、小胶质细胞/内皮细胞用NN - 1、少突胶质细胞用6D2)的双标记免疫组织化学方法,我们证明,与正常动物一样,表达ephrin - A2的细胞仅为神经元。此外,用BrdU进行双标记显示,ephrin - A2在驻留细胞中表达,而非在视神经再生过程中产生的细胞中表达[《脑研究》854卷(2000年)178页,153卷(1978年)345页]。