Dahlström A B, Czernik A J, Li J Y
Department of Histology, NRCG, University of Göteborg, Sweden.
Mol Neurobiol. 1992 Summer-Fall;6(2-3):157-77. doi: 10.1007/BF02780550.
The present minireview describes experiments carried out, in short-term crush-operated rat nerves, using immunofluorescence and cytofluorimetric scanning techniques to study endogenous substances in anterograde and retrograde fast axonal transport. Vesicle membrane components p38 (synaptophysin) and SV2 are accumulating on both sides of a crush, but a larger proportion of p38 (about 3/4) than of SV2 (about 1/2) is recycling toward the cell body, compared to the amount carried with anterograde transport. Matrix peptides, such as CGRP, ChRA, VIP, and DBH are recycling to a minor degree, although only 10-20% of surface-associated molecules, such as synapsins and kinesin, appear to recycle. The described methodological approach to study the composition of organelles in fast axonal transport, anterograde as compared to retrograde, is shown to be useful for investigating neurobiological processes. We make use of the "in vivo chromatography" process that the fast axonal transport system constitutes. Only substances that are in some way either stored in, or associated with, transported organelles can be clearly observed to accumulate relative to the crush region. Emphasis in this paper was given to the synapsins, because of diverging results published concerning the degree of affiliation with various neuronal organelles. Our previously published results have indicated that in the living axons the SYN I is affiliated with mainly anterogradely fast transported organelles. Therefore, some preliminary, previously unpublished results on the accumulations of the four different synapsins (SYN Ia, SYN Ib, SYN IIa, and SYN IIb), using antisera specific for each of the four members of the synapsin family, are described. It was found that SYN Ib clearly has a stronger affiliation to anterogradely transported organelles than SYN Ia, and that both SYN IIa and SYN IIb are bound to some degree to transported organelles.
本微型综述描述了在短期挤压处理的大鼠神经中进行的实验,使用免疫荧光和细胞荧光扫描技术研究顺行和逆行快速轴突运输中的内源性物质。囊泡膜成分p38(突触素)和SV2在挤压部位两侧积累,但与顺行运输携带的量相比,p38(约3/4)比SV2(约1/2)有更大比例向细胞体循环。基质肽,如降钙素基因相关肽(CGRP)、生长激素释放肽相关肽(ChRA)、血管活性肠肽(VIP)和多巴胺β-羟化酶(DBH)的循环程度较小,尽管只有10%-20%的表面相关分子,如突触结合蛋白和驱动蛋白,似乎会循环。所描述的研究快速轴突运输中细胞器组成(顺行与逆行相比)的方法,被证明对研究神经生物学过程有用。我们利用快速轴突运输系统构成的“体内色谱”过程。只有以某种方式存储在运输细胞器中或与之相关的物质,才能明显观察到相对于挤压区域的积累。由于关于与各种神经元细胞器的关联程度发表了不同结果,本文重点关注突触结合蛋白。我们之前发表的结果表明,在活轴突中,SYN I主要与顺行快速运输的细胞器相关。因此,描述了一些关于四种不同突触结合蛋白(SYN Ia、SYN Ib、SYN IIa和SYN IIb)积累的初步、之前未发表的结果,使用针对突触结合蛋白家族四个成员各自的抗血清。发现SYN Ib与顺行运输细胞器的关联明显强于SYN Ia,并且SYN IIa和SYN IIb都在一定程度上与运输细胞器结合。