Vígh B, Manzano e Silva M J, Frank C L, Vincze C, Czirok S J, Szabó A, Lukáts A, Szél A
Department of Human Morphology and Developmental Biology, Semmelweis University, Budapest, Hungary.
Histol Histopathol. 2004 Apr;19(2):607-28. doi: 10.14670/HH-19.607.
Recent investigations confirm the importance of nonsynaptic signal transmission in several functions of the nervous tissue. Present in various periventricular brain regions of vertebrates, the system of cerebrospinal fluid (CSF)-contacting neurons seems to have a special role in taking up, transforming and emitting nonsynaptic signals mediated by the internal and external CSF and intercellular fluid of the brain. Most of the CSF-contacting nerve cells send dendritic processes into the internal CSF of the brain ventricles or central canal where they form terminals bearing stereocilia and a 9+0-, or 9+2-type cilium. Some of these neurons resemble known sensory cells of chemoreceptor-type, others may be sensitive to the pressure or flow of the CSF, or to the illumination of the brain tissue. The axons of the CSF-contacting neurons transmit information taken up by dendrites and perikarya to synaptic zones of various brain areas. By forming neurohormonal terminals, axons also contact the external CSF space and release various bioactive substances there. Some perikarya send their axons into the internal CSF, and form free endings there, or synapses on intraventricular dendrites, perikarya and/or on the ventricular surface of ependymal cells. Contacting the intercellular space, sensory-type cilia were also demonstrated on nerve cells situated in the brain tissue subependymally or farther away from the ventricles. Among neuronal elements entering the internal CSF-space, the hypothalamic CSF-contacting neurons are present in the magnocellular and parvicellular nuclei and in some circumventricular organs like the paraventricular organ and the vascular sac. The CSF-contacting dendrites of all these areas bear a solitary 9 x 2+0-type cilium and resemble chemoreceptors cytologically. In electrophysiological experiments, the neurons of the paraventricular organ are highly sensitive to the composition of the ventricular CSF. The axons of the CSF-contacting neurons terminate not only in the hypothalamic synaptic zones but also in tel-, mes- and rhombencephalic nuclei and reach the spinal cord as well. The supposed chemical information taken up by the CSF-contacting neurons from the ventricular CSF may influence the function of these areas of the central nervous system. Some nerve cells of the photoreceptor areas form sensory terminals similar to those of the hypothalamic CSF-contacting neurons. Special secondary neurons of the retina and pineal organ contact the retinal photoreceptor space and pineal recess respectively, both cavities being embryologically derived from the 3rd ventricle. The composition of these photoreceptor spaces is important in the photochemical transduction and may modify the activity of the secondary neurons. Septal and preoptic CSF-contacting neurons contain various opsins and other compounds of the phototransduction cascade and represent deep encephalic photoreceptors detecting the illumination of the brain tissue and play a role in the regulation of circadian and reproductive responses to light. The medullo-spinal CSF-contacting neurons present in the oblongate medulla, spinal cord and terminal filum, send their dendrites into the fourth ventricle and central canal. Resembling mechanoreceptors of the lateral line organ, the spinal CSF-contacting neurons may be sensitive to the pressure or flow of the CSF. The axons of these neurons terminate at the external CSF-space of the oblongate medulla and spinal cord and form neurohormonal nerve endings. Based on information taken up from the CSF, a regulatory effect on the production or composition of CSF was supposed for bioactive materials released by these terminals. Most of the axons of the medullospinal CSF-contacting neurons and the magno- and parvicellular neurosecretory nuclei running to neurohemal areas (neurohypophysis, median eminence, terminal lamina, vascular sac and urophysis) do not terminate directly on vessels, instead they form neurohormonal nerve terminals attached by half-desmosomes on the basal lamina of the external and vascular surface of the brain tissue. Therefore, the bioactive materials released from these terminals primarily enter the external CSF and secondarily, by diffusion into vessels and the composition of the external CSF, may have a modulatory effect on the bioactive substances released by the neurohormonal terminals. Contacting the intercellular space, sensory-type cilia were also demonstrated on nerve cells situated subependymally or farther away from the ventricles, among others in the neurosecretory nuclei. Since tight-junctions are lacking between ependymal cells of the ventricular wall, not only CSF-contacting but also subependymal ciliated neurons may be influenced by the actual composition of the CSF besides that of the intercellular fluid of the brain tissue. According to the comparative histological data summarised in this review, the ventricular CSF-contacting neurons represent the phylogenetically oldest component detecting the internal fluid milieu of the brain. The neurohormonal terminals on the external surface of the brain equally represent an ancient form of nonsynaptic signal transmission.
最近的研究证实了非突触信号传递在神经组织多种功能中的重要性。脑脊液(CSF)接触神经元系统存在于脊椎动物的各个脑室周围脑区,似乎在摄取、转化和释放由脑内、外脑脊液以及细胞间液介导的非突触信号方面具有特殊作用。大多数脑脊液接触神经细胞将树突过程伸入脑室或中央管的脑内脑脊液中,在那里它们形成带有静纤毛和9+0或9+2型纤毛的终末。这些神经元中的一些类似于已知的化学感受器型感觉细胞,其他一些可能对脑脊液的压力或流动、或对脑组织的光照敏感。脑脊液接触神经元的轴突将树突和胞体摄取的信息传递到各个脑区的突触区。通过形成神经激素终末,轴突还与外部脑脊液空间接触并在那里释放各种生物活性物质。一些胞体将其轴突伸入脑内脑脊液,并在那里形成游离终末,或在脑室内树突、胞体和/或室管膜细胞的室表面形成突触。在位于脑室下或远离脑室的脑组织中的神经细胞上也发现了接触细胞间空间的感觉型纤毛。在进入脑内脑脊液空间的神经元成分中,下丘脑脑脊液接触神经元存在于大细胞和小细胞核以及一些室周器官,如室旁器官和血管囊。所有这些区域的脑脊液接触树突都带有一根单独的9×2+0型纤毛,在细胞学上类似于化学感受器。在电生理实验中,室旁器官的神经元对脑室脑脊液的成分高度敏感。脑脊液接触神经元的轴突不仅终止于下丘脑突触区,还终止于端脑、中脑和后脑的核团,甚至到达脊髓。脑脊液接触神经元从脑室脑脊液中摄取的假定化学信息可能会影响中枢神经系统这些区域的功能。光感受器区域的一些神经细胞形成类似于下丘脑脑脊液接触神经元的感觉终末。视网膜和松果体器官的特殊二级神经元分别接触视网膜光感受器空间和松果体隐窝,这两个腔在胚胎学上均源自第三脑室。这些光感受器空间的成分在光化学转导中很重要,并且可能改变二级神经元的活性。隔区和视前区脑脊液接触神经元含有各种视蛋白和光转导级联反应的其他化合物,代表检测脑组织光照的深部脑光感受器,并在昼夜节律和对光的生殖反应调节中发挥作用。延髓-脊髓脑脊液接触神经元存在于延髓、脊髓和终丝中,它们将树突伸入第四脑室和中央管。类似于侧线器官的机械感受器,脊髓脑脊液接触神经元可能对脑脊液的压力或流动敏感。这些神经元的轴突终止于延髓和脊髓的外部脑脊液空间,并形成神经激素神经终末。基于从脑脊液中摄取的信息,推测这些终末释放的生物活性物质对脑脊液的产生或成分具有调节作用。延髓脊髓脑脊液接触神经元以及大细胞和小细胞神经分泌核的大多数轴突通向神经血器官(神经垂体、正中隆起、终板、血管囊和尿体),它们并不直接终止于血管,而是在脑组织外部和血管表面的基膜上通过半桥粒形成神经激素神经终末。因此,从这些终末释放的生物活性物质首先进入外部脑脊液,其次通过扩散进入血管,并且外部脑脊液的成分可能对神经激素终末释放的生物活性物质具有调节作用。在位于脑室下或远离脑室的神经细胞上也发现了接触细胞间空间的感觉型纤毛,其中包括神经分泌核中的神经细胞。由于脑室壁的室管膜细胞之间缺乏紧密连接,除了脑组织的细胞间液外,脑脊液接触神经元和脑室下带纤毛神经元都可能受到脑脊液实际成分的影响。根据本综述总结的比较组织学数据,脑室脑脊液接触神经元代表了在系统发育上检测脑内液体环境最古老的成分。脑外表面的神经激素终末同样代表了非突触信号传递的一种古老形式。