Neuronal morphology and the synaptic organisation of sympathetic ganglia

I.L. Gibbins, P. Jobling, J.P. Messenger, E.H. Teo, J.L. Morris
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引用次数: 39

Abstract

In this article, we provide a short review of the structure and synaptic organisation of the final motor neurons in the sympathetic ganglia of mammals. Combinations of pathway tracing, multiple-labelling immunofluorescence and intracellular dye injection have shown that neurons in different functional pathways differ not only in their patterns of neuropeptide expression, but also in the size of their cell bodies and dendritic fields. Thus, vasoconstrictor neurons consistently are smaller than any other major functional class of neurons. Serial section ultrastructural analysis of dye filled neurons, together with electron microscopic and confocal microscopic analysis of immunolabelled synaptic inputs to sympathetic final motor neurons indicate that synapses are rare and randomly distributed over the surface of the neurons. The total number of synapses is simply proportional to the total surface area of the neurons. Many terminal boutons of peptide-containing preganglionic neurons do not make conventional synapses with target neurons. Furthermore, there is a spatial mismatch in the distribution of peptide-containing terminals and neurons expressing receptors for the corresponding peptides. Together, these results suggest that there are likely to be significant differences in the ways that the final sympathetic motor neurons in distinct functional pathways integrate their synaptic inputs. In at least some pathways, heterosynaptic actions of neuropeptides probably contribute to subtle modulation of ganglionic transmission.

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交感神经节的神经元形态和突触组织
本文简要介绍了哺乳动物交感神经节末段运动神经元的结构和突触组织。途径示踪、多重标记免疫荧光和细胞内染料注射的结合表明,不同功能通路的神经元不仅在神经肽表达模式上存在差异,而且其细胞体和树突状场的大小也存在差异。因此,血管收缩神经元始终小于任何其他主要功能类别的神经元。染色神经元的连续切片超微结构分析,以及免疫标记突触输入到交感终运动神经元的电镜和共聚焦显微镜分析表明,突触是罕见的,随机分布在神经元表面。突触的总数与神经元的总表面积成正比。许多含有肽的神经节前神经元的末端钮扣不与目标神经元形成传统的突触。此外,在含肽末端和表达相应肽受体的神经元的分布中存在空间不匹配。总之,这些结果表明,在不同的功能通路中,最终的交感运动神经元整合突触输入的方式可能存在显著差异。至少在某些途径中,神经肽的异突触作用可能有助于神经节传导的微妙调节。
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