Voutsinos B, Chouaf L, Mertens P, Ruiz-Flandes P, Joubert Y, Belin M F, Didier-Bazes M
INSERM CJF 90-10, Laboratoire d'Anatomie Pathologique, Faculté de Médecine Alexis Carrel, Lyon, France.
Neuroscience. 1994 Apr;59(3):663-72. doi: 10.1016/0306-4522(94)90185-6.
During development, recognition mechanisms between neurons and their targets are necessary for the formation of the neuronal network. Neural connections are synaptic or non-junctional. Both types of communication can be found between neurons and glial elements in the periventricular walls. Serotonergic fibers form synaptic contacts on the specialized ependymocytes of the subcommissural organ, a structure which forms the roof of the third ventricle at its junction with the aqueduct. A network of non-junctional fibers containing both GABA and serotonin spread between the cilia of the classical ependymocytes in the ventricles. These anatomical, morphological and biochemical features suggest a tropism and specific recognition mechanisms between glial elements and serotonergic neurons. This hypothesis can be tested by the study of the innervation of the subcommissural organ and the classical ependyma by grafted embryonic neurons after a chemical destruction of the serotonergic endogenous innervation. Solid implants or cell suspensions prepared from embryonic metencephalon were transplanted to either the third ventricle or the periventricular gray matter in 5,7-dihydroxytryptamine denervated rats. Grafted serotonergic neurons were able to reinnervate the classical ependyma and the subcommissural organ. The fibers forming the supraependymal plexus were non-junctional and contained both serotonin and GABA while those innervating the subcommissural organ formed synaptic contacts and contained only serotonin. The signals capable of inducing the ependymal innervation were specific for serotonergic neurons since catecholaminergic neurons present in the grafts were unable to innervate either classical or specialized ependymocytes. These results demonstrate that glial cells are targets for serotonergic neurons and that the morphological and biochemical characteristics of the serotonergic innervation are closely related to the target cell phenotype.
在发育过程中,神经元与其靶标之间的识别机制对于神经网络的形成是必要的。神经连接分为突触连接和非连接性连接。这两种通讯方式都可在脑室壁的神经元与神经胶质成分之间找到。5-羟色胺能纤维在联合下器官的特化室管膜细胞上形成突触连接,联合下器官是在第三脑室与导水管交界处形成第三脑室顶部的结构。一个包含γ-氨基丁酸(GABA)和5-羟色胺的非连接性纤维网络在脑室中典型室管膜细胞的纤毛之间扩散。这些解剖学、形态学和生化特征表明神经胶质成分与5-羟色胺能神经元之间存在趋向性和特异性识别机制。这个假设可以通过在化学破坏内源性5-羟色胺能神经支配后,研究移植的胚胎神经元对联合下器官和典型室管膜的神经支配来进行验证。将由胚胎后脑制备的实体植入物或细胞悬液移植到5,7-二羟基色胺去神经支配大鼠的第三脑室或脑室周围灰质中。移植的5-羟色胺能神经元能够重新支配典型室管膜和联合下器官。形成室管膜上丛的纤维是非连接性的,同时含有5-羟色胺和GABA,而支配联合下器官的纤维形成突触连接,且仅含有5-羟色胺。能够诱导室管膜神经支配的信号对5-羟色胺能神经元具有特异性,因为移植中存在的儿茶酚胺能神经元无法支配典型或特化的室管膜细胞。这些结果表明神经胶质细胞是5-羟色胺能神经元的靶标,并且5-羟色胺能神经支配的形态学和生化特征与靶细胞表型密切相关。