Vigh-Teichmann I, Vigh B
Arch Histol Jpn. 1983 Sep;46(4):427-68. doi: 10.1679/aohc.46.427.
Cerebrospinal fluid (CSF)-contacting neurons are located periventricularly or inside the brain ventricles; they contact the CSF via their dendrites, perikarya or axons. Most of the CSF-contacting nerve cells send dendritic processes into the ventricular cavity where they form ciliated terminals. These ciliated dendritic endings resemble those of known sensory cells, yet their role is still unknown. There are two types of CSF-contacting dendritic terminals. One bears solitary 9 X 2 + 0 cilia; it is present in different hypothalamic regions such as the paraventricular organ and the vascular sac. The magnocellular neurosecretory nuclei also contain CSF-contacting neurons, which probably furnish information about the parameters of the CSF for the regulatory function of the hypothalamo-hypophyseal system. CSF-contacting nerve cells of the parvocellular hypothalamic nuclei are suspected to participate in hypothalamo-adenohypophyseal regulation. A second type of CSF-contacting dendritic terminal bears many stereocilia and is found in the central canal of the spinal cord. This type of terminal is also supplied with a 9 X 2 + 2 kinocilium that may contact Reissner's fiber, the secretory material of the subcommissural organ. Resembling mainly mechanoreceptors, these spinal CSF-contacting neurons appear to form axon terminals of the neurosecretory type at the external circumference of the spinal cord. Developing and/or regressing photoreceptor cells of the retina and pineal complex may display a similar dendritic structure characteristic of hypothalamic CSF-contacting neurons. Axons penetrating into the ventricles innervate the apical surface of the ependyma and/or the CSF-contacting dendritic terminals. Some bipolar neurons of the retina form so-called Landolt's clubs; these may be considered as the retinal component of the CSF-contacting neuronal system. Since in the lancelet nearly all nerve cells contact the CSF, the CSF-contacting neurons represent a specialized, but phylogenetically old cell type, a "protoneuron" in the vertebrate brain. They may be derived phylogenetically by inversion of the ciliated neurons found in the plate-like nervous system of more primitive deuterostomians.
脑脊液接触神经元位于脑室周围或脑室内;它们通过树突、胞体或轴突与脑脊液接触。大多数脑脊液接触神经细胞将树突突起发送到脑室腔内,在那里形成纤毛终末。这些有纤毛的树突末梢类似于已知的感觉细胞的末梢,但其作用仍然未知。有两种类型的脑脊液接触树突终末。一种带有单个9×2 + 0纤毛;它存在于不同的下丘脑区域,如室旁器官和血管囊。大细胞神经分泌核也含有脑脊液接触神经元,它们可能为下丘脑 - 垂体系统的调节功能提供有关脑脊液参数的信息。下丘脑小细胞神经核的脑脊液接触神经细胞被怀疑参与下丘脑 - 腺垂体调节。第二种类型的脑脊液接触树突终末有许多静纤毛,见于脊髓中央管。这种终末还配有一根9×2 + 2动纤毛,可能与连合下器官的分泌物质瑞氏纤维接触。这些脊髓脑脊液接触神经元主要类似于机械感受器,似乎在脊髓外周形成神经分泌型轴突终末。视网膜和松果体复合体中发育和/或退化的光感受器细胞可能表现出类似于下丘脑脑脊液接触神经元的树突结构特征。穿透脑室的轴突支配室管膜的顶面和/或脑脊液接触树突终末。视网膜的一些双极神经元形成所谓的兰多尔特小体;这些可被视为脑脊液接触神经元系统的视网膜成分。由于在文昌鱼中几乎所有神经细胞都与脑脊液接触,脑脊液接触神经元代表一种特化但在系统发育上古老的细胞类型,是脊椎动物脑中的“原神经元”。它们可能在系统发育上由更原始的后口动物板状神经系统中发现的纤毛神经元倒置而来。