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突触质膜和突触小泡膜抗原的免疫化学比较。

Immunochemical comparison of synaptic plasma membrane and synaptic vesicle membrane antigens.

作者信息

Howe P R, Fenwick E M, Rostas J A, Livett B G

出版信息

J Neurocytol. 1977 Jun;6(3):339-52. doi: 10.1007/BF01175195.

Abstract

A synaptic vesicle fraction and a synaptic plasma membrane fraction obtained after subfractionation of synaptosomes from chick forebrain have been used to produce antisera in rabbits. Immunofluorescence histology with the two antisera revealed that they reacted strongly with synaptic terminal regions present in the chick forebrain, cerebellum and spinal cord. In addition, the synaptic plasma membrane antiserum (but not the synaptic vesicle antiserum) reacted with preterminal axons in the cerebellum and spinal cord. Comparison of the two antisera by two-dimensional immunoelectrophoresis, revealed the presence of common antigens in the synaptosomal vesicle and plasma membrane fractions. Incubation of synaptosomes in vitro with the synaptosomal vesicle antiserum and complement produced a dose-dependent inhibition of synaptosome swelling up to a maximum of 55% of that obtained with the synaptosomal plasma membrane antiserum. The results of this test are consistent with the hypothesis that some synaptosomal vesicle antigens may be present also in the synaptosomal plasma membrane and imply that they face the external surface of the synaptosomes. The fate of vesicle membrane components in synaptosomal plasma membranes is not known. The possibility is discussed that they may be recycled locally by a mechanism similar to that proposed by Heuser and Reese (1973) for re-use of synaptic vesicle membranes at the neuromuscular junction.

摘要

从鸡前脑的突触体亚分级分离后获得的突触小泡组分和突触质膜组分已被用于在兔体内产生抗血清。用这两种抗血清进行免疫荧光组织学研究表明,它们与鸡前脑、小脑和脊髓中存在的突触终末区域强烈反应。此外,突触质膜抗血清(而非突触小泡抗血清)与小脑和脊髓中的终末前轴突发生反应。通过二维免疫电泳对这两种抗血清进行比较,发现在突触体小泡和质膜组分中存在共同抗原。体外将突触体与突触体小泡抗血清及补体一起孵育,可产生剂量依赖性的突触体肿胀抑制,最大抑制程度可达突触体质膜抗血清所获抑制程度的55%。该试验结果与以下假说一致,即某些突触体小泡抗原可能也存在于突触体质膜中,这意味着它们面向突触体的外表面。突触体膜中囊泡膜成分的命运尚不清楚。文中讨论了一种可能性,即它们可能通过类似于Heuser和Reese(1973年)提出的在神经肌肉接头处重新利用突触小泡膜的机制在局部进行循环利用。

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