Kotrschal K, Lametschwandtner A, Adam H
J Hirnforsch. 1985;26(3):333-51.
The fine structure and vascular supply of the median eminence (ME) was studied in 57 specimens of Acipenser ruthenus (Chondrostei) by means of light microscopy (normal histology, horseradish-peroxidase (HRP), formaldehyde induced fluorescence (FIF), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) as well as by SEM of vascular corrosion casts. Light microscopy revealed that the ME increases in thickness from caudal to rostral with capillaries invading the subependymal layers only at the rostral median eminence (rME). At the middle (mME) and caudal median eminence (cME) capillaries are limited to the ME outer surface. Short term HRP-application (systemically as well as intraventricularly) resulted in reaction product in the intercellular space throughout the ME after a survival time of 2 hours. The ME tanycytes were distinctly marked after 7 days survival. FIF revealed aminergic cerebrospinal fluid (CSF-) contacting neurons; also the apical part of tanycytes showed specific fluorescence. SEM of vascular corrosion casts showed that the arterial supply of the whole ME results from branches of the hypothalamic artery and/or from those arteries supplying the saccus vasculosus. The whole 2-dimensional primary capillary plexus of the ME drains via portal vessels into the adenohypophysis. As demonstrated by SEM, the ME ependymal surface is made up by oligociliated tanycytes, abundant crown cells and intraventricular protrusions of CSF-contacting neurons. Supraependymal cells are lacking, supraependymal fibres are very sparse. TEM revealed the ME tanycytes with long ciliary rootlets. Their basal processes split into numerous delicate branches forming many end-feet, which end at the basal lamina opposite the fenestrated capillaries of the primary plexus. Like tanycytes, also the crown cells possess branching processes which may contribute to the outer glial membrane. CSF-contacting neurons of the type I (with dense core vesicles ranging in diameter from 100-120 nm and of presumed aminergic nature) and type II (with dense core vesicles ranging in diameter from 160-180 nm and of presumed peptidergic nature) were found. Both types are most abundant in the cME. Small astrocytes reveal delicate processes which cover parts of the CSF-contacting neurons and of tanycytes. Another glial cell type is situated near the basal lamina and forms processes parallel the latter. There are few axo-somal and axo-axonal synapses pointing rather to a humoral regulation of the ME with signals from the ME blood vascular bed or from the CSF acting on CSF-contacting neurons.
利用光学显微镜(常规组织学、辣根过氧化物酶(HRP)、甲醛诱导荧光(FIF))、扫描电子显微镜(SEM)和透射电子显微镜(TEM)以及血管铸型扫描电子显微镜,对57个俄罗斯鲟(软骨硬鳞鱼)标本的正中隆起(ME)的精细结构和血管供应进行了研究。光学显微镜显示,ME从尾侧向吻侧厚度增加,只有在吻侧正中隆起(rME)处毛细血管侵入室管膜下层。在中(mME)和尾侧正中隆起(cME)处,毛细血管仅限于ME外表面。短期全身及脑室内应用HRP,2小时存活期后,整个ME的细胞间隙出现反应产物。存活7天后,ME的伸长细胞被明显标记。FIF显示胺能性脑脊液(CSF)接触神经元;伸长细胞的顶端部分也显示出特异性荧光。血管铸型扫描电子显微镜显示,整个ME的动脉供应来自下丘脑动脉分支和/或供应血管囊的动脉分支。ME的整个二维初级毛细血管丛通过门静脉引流到腺垂体。扫描电子显微镜显示,ME的室管膜表面由少纤毛伸长细胞、丰富的冠细胞和CSF接触神经元的脑室内突起组成。缺乏室管膜上细胞,室管膜上纤维非常稀疏。透射电子显微镜显示ME的伸长细胞有长的睫状小根。它们的基底突分成许多细小分支,形成许多终足,终止于与初级丛有窗孔的毛细血管相对的基膜处。与伸长细胞一样,冠细胞也有分支突起,可能有助于形成外胶质膜。发现了I型(致密核心囊泡直径为100 - 120 nm,推测为胺能性质)和II型(致密核心囊泡直径为160 - 180 nm,推测为肽能性质)的CSF接触神经元。两种类型在cME中最为丰富。小星形胶质细胞有精细的突起,覆盖部分CSF接触神经元和伸长细胞。另一种胶质细胞类型位于基膜附近,形成与基膜平行的突起。存在少量轴体和轴-轴突触,这表明ME的体液调节是由来自ME血管床或CSF的信号作用于CSF接触神经元实现的。