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Neuron. 1995 Jul;15(1):115-26. doi: 10.1016/0896-6273(95)90069-1.

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The dystroglycan complex is necessary for stabilization of acetylcholine receptor clusters at neuromuscular junctions and formation of the synaptic basement membrane.肌营养不良蛋白聚糖复合体对于神经肌肉接头处乙酰胆碱受体簇的稳定以及突触基底膜的形成是必需的。
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本文引用的文献

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Muscular dystrophy: dystrophin and partners at the cell surface.肌肉营养不良:抗肌萎缩蛋白及其在细胞表面的相互作用蛋白
Curr Biol. 1993 Feb;3(2):109-11. doi: 10.1016/0960-9822(93)90167-m.
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Dystrophin and the membrane skeleton.肌营养不良蛋白与膜骨架。
Curr Opin Cell Biol. 1993 Feb;5(1):82-7. doi: 10.1016/s0955-0674(05)80012-2.
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The ability of agrin to cluster AChRs depends on alternative splicing and on cell surface proteoglycans.集聚蛋白使乙酰胆碱受体成簇的能力取决于可变剪接和细胞表面蛋白聚糖。
Neuron. 1993 Sep;11(3):491-502. doi: 10.1016/0896-6273(93)90153-i.
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A muscle cell variant defective in glycosaminoglycan biosynthesis forms nerve-induced but not spontaneous clusters of the acetylcholine receptor and the 43 kDa protein.一种在糖胺聚糖生物合成中存在缺陷的肌细胞变体形成了由神经诱导而非自发产生的乙酰胆碱受体和43 kDa蛋白簇。
J Neurosci. 1993 Feb;13(2):586-95. doi: 10.1523/JNEUROSCI.13-02-00586.1993.
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A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.肌营养不良蛋白-糖蛋白复合物作为层粘连蛋白与肌动蛋白之间跨膜连接物的作用。
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6
Laminin-binding protein 120 from brain is closely related to the dystrophin-associated glycoprotein, dystroglycan, and binds with high affinity to the major heparin binding domain of laminin.来自大脑的层粘连蛋白结合蛋白120与肌营养不良蛋白相关糖蛋白肌营养不良聚糖密切相关,并以高亲和力结合层粘连蛋白的主要肝素结合结构域。
J Biol Chem. 1993 Jul 15;268(20):14972-80.
7
Clustering and immobilization of acetylcholine receptors by the 43-kD protein: a possible role for dystrophin-related protein.43-kD蛋白对乙酰胆碱受体的聚集与固定作用:抗肌萎缩蛋白相关蛋白的一种可能作用
J Cell Biol. 1993 Nov;123(3):729-40. doi: 10.1083/jcb.123.3.729.
8
Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor.α- dystroglycan是一种与肌营养不良蛋白相关的糖蛋白,是一种功能性聚集蛋白受体。
Cell. 1994 Jun 3;77(5):675-86. doi: 10.1016/0092-8674(94)90052-3.
9
A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering.肌营养不良蛋白相关糖蛋白和抗肌萎缩蛋白在聚集蛋白诱导的乙酰胆碱受体聚集中的作用。
Cell. 1994 Jun 3;77(5):663-74. doi: 10.1016/0092-8674(94)90051-5.
10
Dystrophin-associated proteins and synapse formation: is alpha-dystroglycan the agrin receptor?肌营养不良蛋白相关蛋白与突触形成:α- dystroglycan是聚集蛋白受体吗?
Cell. 1994 Jun 3;77(5):617-9. doi: 10.1016/0092-8674(94)90045-0.

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.

DOI:10.1083/jcb.129.4.1093
PMID:7744958
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2120479/
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。