Schweitzer L, Cant N B
J Comp Neurol. 1984 May 10;225(2):228-43. doi: 10.1002/cne.902250208.
The development of cochlear fibers and terminals in the dorsal cochlear nucleus of the hamster was studied with light and electron microscopic techniques. Like the dorsal cochlear nucleus of most other mammals, the dorsal cochlear nucleus of the adult hamster is a laminated structure. Three distinct layers can be identified in cresyl-violet-stained sections: the molecular layer, the fusiform cell layer, and the deep layer. The deep layer consists of a superficial zone, free of large cell bodies, and a deep zone which contains the somas of giant cells. Horseradish peroxidase and degeneration studies reveal that the cochlear fibers ramify throughout the deep and fusiform cell layers of the adult hamster but do not enter the molecular layer. In the electron microscope, three types of terminals that contact the fusiform and the giant cells can be distinguished. Only one type of terminal (type LR) degenerates after cochlear ablation and is, therefore, thought to be of cochlear origin. Type LR terminals are found throughout the deep and fusiform cell layers and contact the somas of giant and fusiform cells, as well as their intermingled dendrites in the deep layer. In Golgi-impregnated material, cochlear fibers are not found in the dorsal cochlear nucleus of the neonatal hamster, although they have entered the ventral cochlear nucleus. Ingrowth of cochlear fibers into the dorsal cochlear nucleus occurs over the first postnatal week and one-half. A spatial gradient is evident during the ingrowth of the fibers in that they invade the dorsomedial parts of the dorsal cochlear nucleus before they invade the ventrolateral parts. In all parts of the nucleus, the fibers enter the deepest layer and grow progressively more superficially. In the electron microscope, the first appearance of type LR terminals at each depth lags behind the ingrowth of the fibers by about two days. In hamsters, fibers from the basal turns of the cochlea terminate in the dorsomedial dorsal cochlear nucleus, while fibers from the apical turns terminate in the ventrolateral dorsal cochlear nucleus (DCN). The dorsomedial to ventrolateral gradient in the ingrowth of the cochlear fibers into the DCN indicates that the fibers from the basal turn are the first to arrive. Several components of the mammalian cochlea have been shown to mature at the base of the cochlea before they mature at the apex. The present study suggests that maturation gradients in the cochlear nucleus parallel those observed in the cochlea.
采用光镜和电镜技术研究了仓鼠蜗背侧核中蜗神经纤维和终末的发育。与大多数其他哺乳动物的蜗背侧核一样,成年仓鼠的蜗背侧核是一种分层结构。在甲酚紫染色切片中可识别出三个不同的层:分子层、梭形细胞层和深层。深层由一个不含大细胞体的浅区和一个含有巨细胞胞体的深区组成。辣根过氧化物酶和溃变研究表明,蜗神经纤维在成年仓鼠的深层和梭形细胞层中分支,但不进入分子层。在电子显微镜下,可以区分出与梭形细胞和巨细胞接触的三种终末类型。只有一种终末类型(LR型)在蜗神经切断后发生溃变,因此被认为起源于蜗神经。LR型终末见于整个深层和梭形细胞层,与巨细胞和梭形细胞的胞体及其在深层中交织的树突接触。在高尔基染色标本中,虽然蜗神经纤维已进入蜗腹侧核,但在新生仓鼠的蜗背侧核中未发现蜗神经纤维。蜗神经纤维在出生后的第一周半内长入蜗背侧核。在纤维长入过程中,空间梯度明显,即它们在侵入蜗背侧核的腹外侧部分之前先侵入背内侧部分。在核的所有部分,纤维进入最深层并逐渐向浅层生长。在电子显微镜下,每种深度的LR型终末的首次出现比纤维长入滞后约两天。在仓鼠中,来自蜗基底转的纤维终止于蜗背侧核的背内侧,而来自蜗顶转的纤维终止于蜗背侧核的腹外侧(DCN)。蜗神经纤维长入DCN的背内侧到腹外侧梯度表明,来自基底转的纤维最先到达。哺乳动物蜗的几个组成部分已被证明在蜗基底先成熟,然后在蜗顶成熟。本研究表明,蜗背侧核中的成熟梯度与蜗中观察到的梯度平行。