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胚胎期神经-肌肉突触形成过程中α- dystroglycan的分布

Distribution of alpha-dystroglycan during embryonic nerve-muscle synaptogenesis.

作者信息

Cohen M W, Jacobson C, Godfrey E W, Campbell K P, Carbonetto S

机构信息

Department of Physiology, McGill University, Montreal, Quebec, Canada.

出版信息

J Cell Biol. 1995 May;129(4):1093-101. doi: 10.1083/jcb.129.4.1093.

Abstract

The distribution of alpha-dystroglycan (alpha DG) relative to acetylcholine receptors (AChRs) and neural agrin was examined by immunofluorescent staining with mAb IIH6 in cultures of nerve and muscle cells derived from Xenopus embryos. In Western blots probed with mAb IIH6, alpha DG was evident in membrane extracts of Xenopus muscle but not brain. alpha DG immunofluorescence was present at virtually all synaptic clusters of AChRs and neural agrin. Even microclusters of AChRs and agrin at synapses no older than 1-2 h (the earliest examined) had alpha DG associated with them. alpha DG was also colocalized at the submicrometer level with AChRs at nonsynaptic clusters that have little or no agrin. The number of large (> 4 microns) nonsynaptic clusters of alpha DG, like the number of large nonsynaptic clusters of AChRs, was much lower on innervated than on noninnervated cells. When mAb IIH6 was included in the culture medium, the large nonsynaptic clusters appeared fragmented and less compact, but the accumulation of agrin and AChRs along nerve-muscle contacts was not prevented. It is concluded that during nerve-muscle synaptogenesis, alpha DG undergoes the same nerve-induced changes in distribution as AChRs. We propose a diffusion trap model in which the alpha DG-transmembrane complex participates in the anchoring and recruitment of AChRs and alpha DG during the formation of synaptic as well as nonsynaptic AChR clusters.

摘要

利用单克隆抗体IIH6进行免疫荧光染色,在源自非洲爪蟾胚胎的神经和肌肉细胞培养物中,检测了α- dystroglycan(α-DG)相对于乙酰胆碱受体(AChRs)和神经聚集蛋白的分布情况。在用单克隆抗体IIH6探测的蛋白质免疫印迹中,α-DG在非洲爪蟾肌肉而非大脑的膜提取物中明显可见。α-DG免疫荧光几乎出现在所有AChRs和神经聚集蛋白的突触簇中。即使是突触处不超过1-2小时(检测的最早时间)的AChRs和聚集蛋白微簇也有与之相关的α-DG。在几乎没有或没有聚集蛋白的非突触簇中,α-DG也在亚微米水平上与AChRs共定位。与AChRs的大的(>4微米)非突触簇数量一样,α-DG的大的非突触簇数量在受神经支配的细胞上比在未受神经支配的细胞上要低得多。当单克隆抗体IIH6包含在培养基中时,大的非突触簇看起来破碎且不那么紧密,但神经肌肉接触处聚集蛋白和AChRs的积累并未受到阻止。得出结论:在神经肌肉突触形成过程中,α-DG经历与AChRs相同的神经诱导分布变化。我们提出一种扩散陷阱模型,其中α-DG跨膜复合物在突触以及非突触AChR簇形成过程中参与AChRs和α-DG的锚定和募集。

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