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培养的脊髓神经元中突触小泡的动力学与突触形成的关系。

Dynamics of synaptic vesicles in cultured spinal cord neurons in relationship to synaptogenesis.

作者信息

Dai Z, Peng H B

机构信息

Department of Cell Biology and Anatomy, University of North Carolina, Chapel Hill 27599-7090, USA.

出版信息

Mol Cell Neurosci. 1996 Jun;7(6):443-52. doi: 10.1006/mcne.1996.0032.

Abstract

The dynamics of synaptic vesicles (SVs) during the development of presynaptic specializations in cultured Xenopus spinal cord neurons was studied with the fluorescent vesicular probe FM1-43. In naive neurons that have not contacted synaptic targets, packets of SVs are distributed along the entire neurite and are quite mobile. The interaction with the synaptic target, such as a muscle cell or a latex bead coated with basic fibroblast growth factor, results in the localization and immobilization of SV packets at the contact site. Depolarization resulted in exocytosis of SVs in both naive and target-contacted neurites. Okadaic acid, a phosphatase inhibitor, caused a dispersal of SV packets in both naive and target-contacted neurites. Thus, prior to target contact, SVs are already organized into packets capable of release and recycling by a phosphorylation-dependent mechanism. Target interaction then recruits and anchors these functional SV packets into forming the presynaptic nerve terminal. With fluorescent phalloidin as a probe, F-actin was found to colocalize with SV clusters at bead-neurite contacts. Although okadaic acid caused a dispersal of SVs at the beads, F-actin localization there was relatively resistant to this drug treatment. This suggests that SVs become localized at the target by interacting with an actin-based cytoskeletal specialization in a phosphorylation-sensitive manner. The induction of this cytoskeletal specialization by the target may be an early event in presynaptic differentiation.

摘要

利用荧光囊泡探针FM1-43,研究了非洲爪蟾脊髓培养神经元突触前特化发育过程中突触囊泡(SVs)的动态变化。在尚未接触突触靶点的未成熟神经元中,成簇的SVs沿整个神经突分布且具有较高的移动性。与突触靶点(如肌肉细胞或包被碱性成纤维细胞生长因子的乳胶珠)的相互作用,导致SVs簇在接触位点定位并固定。去极化导致未成熟神经突和与靶点接触的神经突中SVs的胞吐作用。磷酸酶抑制剂冈田酸导致未成熟神经突和与靶点接触的神经突中SVs簇分散。因此,在靶点接触之前,SVs已经通过磷酸化依赖机制组织成能够释放和循环利用的簇。靶点相互作用随后募集并锚定这些功能性SVs簇,以形成突触前神经末梢。以荧光鬼笔环肽作为探针,发现F-肌动蛋白在珠-神经突接触处与SVs簇共定位。尽管冈田酸导致珠处的SVs分散,但F-肌动蛋白在该处的定位对这种药物处理相对抗性。这表明SVs通过以磷酸化敏感的方式与基于肌动蛋白的细胞骨架特化相互作用而在靶点处定位。靶点对这种细胞骨架特化的诱导可能是突触前分化中的早期事件。

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