McAvoy M, Smith M A, Fujii J T
Department of Anatomy and Cell Biology, Wayne State University of Medicine, Detroit, MI 48201, USA.
Vis Neurosci. 1996 Mar-Apr;13(2):293-301. doi: 10.1017/s0952523800007537.
Agrin is a large extracellular matrix protein that directs the accumulation of acetylcholine receptors at the neuromuscular junction. Recent evidence suggests that agrin may be involved in organizing synapses in the visual system as well. Focussing on the pathway that controls accommodation and pupilloconstriction, this study examined the temporal pattern of agrin expression with reference to the organization of cholinergic synapses between embryonic chick Edinger-Westphal and ciliary ganglion neurons. In situ hybridization with an S35-labeled agrin cRNA probe was used to characterize agrin expression in the Edinger-Westphal nucleus during development. Agrin mRNA was detected in the Edinger-Westphal nucleus at all time points studied, from embryonic day 7 (E7, Hamburger and Hamilton stage 31) through newly hatched chicks. Throughout this period, agrin mRNA expression in Edinger-Westphal neurons was lower than in nearby oculomotor and trochlear neurons, suggesting that cells projecting to neuronal targets may require less agrin than those projecting to muscle. Agrin mRNA expression in the Edinger-Westphal nucleus at E7, E8, E9, and E10 was significantly higher than at E12. The early appearance of agrin mRNA coincides with the period during which acetylcholine receptors are being organized on ciliary ganglion neurons, consistent with the possibility that agrin contributes to neuron-neuron synapse formation in this pathway.
聚集蛋白是一种大型细胞外基质蛋白,它指导乙酰胆碱受体在神经肌肉接头处的聚集。最近的证据表明,聚集蛋白可能也参与了视觉系统中突触的组织过程。本研究聚焦于控制调节和瞳孔收缩的通路,参照胚胎期小鸡动眼神经副核与睫状神经节神经元之间胆碱能突触的组织情况,研究了聚集蛋白表达的时间模式。使用与S35标记的聚集蛋白cRNA探针进行原位杂交,以表征发育过程中动眼神经副核中聚集蛋白的表达情况。在研究的所有时间点,从胚胎第7天(E7,汉伯格和汉密尔顿第31阶段)到新孵出的小鸡,均在动眼神经副核中检测到聚集蛋白mRNA。在此期间,动眼神经副核神经元中聚集蛋白mRNA的表达低于附近的动眼神经和滑车神经神经元,这表明投射到神经元靶点的细胞可能比投射到肌肉的细胞需要更少的聚集蛋白。E7、E8、E9和E10时动眼神经副核中聚集蛋白mRNA的表达明显高于E12时。聚集蛋白mRNA的早期出现与睫状神经节神经元上乙酰胆碱受体正在形成的时期相吻合,这与聚集蛋白有助于该通路中神经元-神经元突触形成的可能性一致。