Hamos J E, King J S
J Comp Neurol. 1980 Nov 15;194(2):441-63. doi: 10.1002/cne.901940210.
The motor nucleus of the opossum trigeminal nerve consists of a main body and a small dorsomedial cell cluster. The cell bodies form a unimodal population with areas that range from 150-2700 mum2. Golgi impregnations reveal that each neuron has three to six primary dendrites which radiate in all planes from the cell body. Within 300 mum from the soma, the primary dendrites divide into secondary branches and these, in turn, bifurcate into thinner distal dendrites. The overall diameter of the dendritic tree often extends as much as 1 mm, with a rare branch leaving the confines of the nucleus to enter the neighboring reticular formation. Somatic and dendritic spines are often present and are either sessile or complex appendage forms. The perikarya and initial dendritic trunks of trigeminal neurons are contacted by four types of presynaptic terminals which cover more than 40% of the membrane. Most endings are 1-3 mum long and contain either spherical (S) or pleomorphic (P) synaptic vesicles. Another, less common, type of bouton is marked by large dense-core (DC) vesicles. Approximately 8% of the terminals on trigeminal cell bodies are large (2-5 mum) with spherical synaptic vesicles and are always associated with a subsynaptic cistern (C-boutons). These terminals very often interdigitate with adjacent synaptic endings. S-, P-, and C-boutons synapse on the dendritic tree of trigeminal neurons in the following characteristic pattern: proximal dendrites (greater than 5 mum in diameter) are contacted by all three types of terminals; intermediate-sized dendrites (between 2.5 and 5.0 mum in diameter) are most often contacted by S-boutons although P-boutons are also present; and small, distal dendrites (less than 2.5 mum in diameter) are almost always contacted by S- boutons. Both S- and P-boutons contact spines. In order to determine the ultrastructural identity of some of the major afferent systems to the trigemina motor nucleus, adult opossums were subjected to two different types of lesions. Three and 5 days subsequent to lesions which destroyed most of the trigeminal mesencephalic nucleus, degenerating terminals containing spherical vesicles were found. These endings were S-boutons on more distal parts of the dendritic tree while on the cell body and proximal dendrites they were C-boutons. Seven days after a mesencephalic lesion, expanded glial processes approximated the trigeminal cell membrane. Two days subsequent to lesions which transected commissural fibers from the contralateral trigeminal complex, degenerating S- and P-boutons were found in contact with intermediate and distal parts of the trigeminal dendritic tree.
负鼠三叉神经运动核由主体和一个小的背内侧细胞簇组成。细胞体形成一个单峰群体,其面积范围为150 - 2700平方微米。高尔基染色显示,每个神经元有三到六个初级树突,从细胞体向各个平面辐射。在距胞体300微米范围内,初级树突分为二级分支,这些二级分支又进一步分叉为更细的远端树突。树突树的总直径通常可达1毫米,很少有分支离开核的范围进入相邻的网状结构。体细胞和树突棘经常存在,要么是无柄的,要么是复杂的附属形式。三叉神经元的胞体和初始树突干与四种类型的突触前终末接触,这些终末覆盖了超过40%的细胞膜。大多数终末长1 - 3微米,含有球形(S)或多形(P)突触小泡。另一种不太常见的终扣类型以大的致密核心(DC)小泡为特征。三叉神经细胞体上约8%的终末较大(2 - 5微米),含有球形突触小泡,并且总是与一个突触下池相关联(C终扣)。这些终末常常与相邻的突触终末相互交错。S、P和C终扣以以下特征模式与三叉神经元的树突树形成突触:近端树突(直径大于5微米)与所有三种类型的终末接触;中等大小的树突(直径在2.5至5.0微米之间)最常与S终扣接触,尽管也有P终扣;而小的远端树突(直径小于2.5微米)几乎总是与S终扣接触。S和P终扣都与棘突接触。为了确定三叉神经运动核一些主要传入系统的超微结构特征,对成年负鼠进行了两种不同类型的损伤。在破坏了大部分三叉神经中脑核的损伤后3天和5天,发现了含有球形小泡的退化终末。这些终末在树突树的更远端部分是S终扣,而在细胞体和近端树突上是C终扣。中脑损伤7天后,扩大的神经胶质突起靠近三叉神经细胞膜。在切断对侧三叉神经复合体的连合纤维的损伤后2天,发现退化的S和P终扣与三叉神经树突树的中间和远端部分接触。