Goshgarian H G, Rafols J A
J Neurocytol. 1984 Feb;13(1):85-109. doi: 10.1007/BF01148320.
Although light microscopic studies have analysed phrenic motor neurons in several different species, there has never been an ultrastructural investigation of identified phrenic motor neurons. In addition, electrophysiological studies have raised questions relating to the function of phrenic motor neurons which may be answered only by direct electron microscopic investigation. Thus, the present study was carried out to provide a detailed ultrastructural analysis of identified phrenic motor neurons. Phrenic motor neurons in the spinal cord of the rat were labelled by retrogradely transported horseradish peroxidase (HRP) after transecting the phrenic nerve in the neck and applying the enzyme directly to the central stump of the transected nerve. The results showed that the general ultrastructural characteristics of phrenic motor neurons were similar to those previously reported for other spinal motor neurons. However, phrenic primary dendrites appeared to be isolated from all other dendritic profiles in the neuropil. Primary dendrites were not fasciculated. Fasciculation occurred only among the more distal secondary and tertiary phrenic dendritic branches. Direct dendrodendritic or dendrosomatic apposition was rarely seen; gap junctions between directly apposing phrenic neuronal membranes were not observed. The membranes of adjacent phrenic neuronal profiles were most frequently separated by intervening sheaths of astroglial processes. Myelinated phrenic axons and a phrenic axon collateral were identified. The initial portion of the phrenic axon collateral was cone-shaped, lacked myelin, and thus resembled a miniature axon hillock. In one instance, a large accumulation of polyribosomes was observed within the hillock-like structure of a phrenic axon collateral. Eight morphological types of synaptic boutons, M, P, NFs, S, NFf, F, G and C were classified according to criteria used by previous investigators. Most of these endings (M, NFs, NFf, S and F) made synaptic contact with profiles of labelled phrenic somata and dendrites. F, NFf, and S boutons also terminated on phrenic axon hillocks. C and G boutons contacted exclusively phrenic somata and small calibre dendrites, respectively. P boutons established axo-axonic synaptic contacts with the M and NFs bouton. The morphological findings of the present study provide new data that may be related to phrenic synchronized output and presynaptic inhibition of primary afferents terminating on phrenic motor neurons.
尽管光学显微镜研究已经分析了几种不同物种的膈运动神经元,但从未有过对已识别的膈运动神经元进行超微结构研究。此外,电生理研究提出了一些与膈运动神经元功能相关的问题,这些问题可能只有通过直接的电子显微镜研究才能得到解答。因此,本研究旨在对已识别的膈运动神经元进行详细的超微结构分析。在颈部横断膈神经并将辣根过氧化物酶(HRP)直接应用于横断神经的中枢残端后,用逆行运输的HRP标记大鼠脊髓中的膈运动神经元。结果表明,膈运动神经元的一般超微结构特征与先前报道的其他脊髓运动神经元相似。然而,膈运动神经元的初级树突似乎与神经毡中的所有其他树突形态分离。初级树突没有成束。成束仅发生在膈运动神经元更远端的二级和三级树突分支之间。很少见到直接的树突 - 树突或树突 - 胞体并置;未观察到直接并置的膈神经元膜之间的缝隙连接。相邻膈神经元形态之间的膜最常被星形胶质细胞突起的中间鞘分隔。识别出了有髓鞘的膈轴突和一条膈轴突侧支。膈轴突侧支的起始部分呈锥形,没有髓鞘,因此类似于一个微型轴突丘。在一个实例中,在膈轴突侧支的丘状结构内观察到大量多核糖体的聚集。根据先前研究者使用的标准,将突触小体分为八种形态类型,即M、P、NFs、S、NFf、F、G和C。这些终末中的大多数(M、NFs、NFf、S和F)与标记的膈运动神经元胞体和树突的形态形成突触联系。F、NFf和S终末也终止于膈运动神经元的轴突丘。C和G终末分别仅与膈运动神经元胞体和小口径树突接触。P终末与M和NFs终末建立轴 - 轴突触联系。本研究的形态学发现提供了可能与膈同步输出以及终止于膈运动神经元的初级传入纤维的突触前抑制相关的新数据。