Literature DB >> 524982

Scanning and transmission electron microscopy of intraventricular dendrite terminals of hypothalamic cerebrospinal fluid contacting neurons in Triturus vulgaris.

I Vigh-Teichmann, B Vigh, B Aros, L Jennes, K Sikora, J Kovács.   

Abstract

A scanning (SEM) and transmission electron microscopic (TEM) study of the ventricular wall of the hypothalamus of Triturus vulgaris was performed with special regard to the intraventricular dendrite terminals of the cerebrospinal fluid (CSF) contacting neurons of the preoptic area (magnocellular and parvocellular preoptic nuclei), the infundibular lobe (anterior periventricular nucleus, infundibular nucleus), and the paraventricular organ. In the preoptic area and infundibular lobe, the terminals were knob-like or club-shaped, of various sizes (diameter about 0,5 to 3,0 micrometer) and located immediately above the ependyma. Ultrastructurally, they may contain dense-core vesicles of varying sizes. The CSF contacting dendrite endings of the paraventricular organ built up a supraependymal labyrinthic layer which could be divided into a rostral crest-like part and a caudal flat and broad division. In both parts, three main types of terminals of various size and shape could be distinguished: a) ramifying, b) elongated, and c) bulb-like dendrite endings which also differed by their TEM structure. The bulk-like terminals, first of all the small ones, originated from the distal part of the nucleus of the organ (nucleus organi paraventricularis) while the other two types took their origin from its intra- and subependymal part. In all areas investigated, each intraventricular dendrite ending gave rise to a solitary cilium (type 9 X 2 + 0). It differed from the ependymal kinocilia by both SEM and TEM characteristics. In the paraventricular organ, the neuronal cilia were hidden inside, or below the supraependymal layer of terminals. There were intraventricular axons which formed synapses on CSF contacting dendrite endings of both parts of the paraventricular organ. Free intraventricular neurons, further ependymal areas heavily or scarcely ciliated, were described. The CSF contacting dendrite terminals were predominantly present near ventricular recesses and in regions where the ependyma was scarcely ciliated.

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Year:  1979        PMID: 524982

Source DB:  PubMed          Journal:  Z Mikrosk Anat Forsch        ISSN: 0044-3107


  7 in total

1.  Cerebrospinal fluid-contacting neurons and other somatostatin-immunoreactive perikarya in brains of tadpoles of Xenopus laevis.

Authors:  S Blähser; I Vigh-Teichmann; M Ueck
Journal:  Cell Tissue Res       Date:  1982       Impact factor: 5.249

2.  The ventricular system of the pigeon brain: a scanning electron microscope study.

Authors:  P Mestres; K Rascher
Journal:  J Anat       Date:  1994-02       Impact factor: 2.610

3.  A Golgi study on the cerebrospinal fluid (CSF)-contacting neurons in the paraventricular nucleus of the Pekin duck.

Authors:  H W Korf; C Viglietti-Panzica; G C Panzica
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

4.  The pineal organ of Raja clavata: opsin immunoreactivity and ultrastructure.

Authors:  I Vigh-Teichmann; B Vigh; M J Manzano e Silva; B Aros
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

5.  The hypothalamo-hypophysial system in Acipenseridae. IX. Formation of monoaminergic neurosecretory cells in the preoptic nucleus region during early ontogeny.

Authors:  A L Polenov; N A Efimova; M S Konstantinova; Y I Senchik; I V Yakovleva
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

6.  CSF-contacting and other somatostatin-immunoreactive neurons in the brains of Anguilla anguilla, Phoxinus phoxinus, and Salmo gairdneri (Teleostei).

Authors:  I Vigh-Teichmann; B Vigh; H W Korf; A Oksche
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

7.  Monoamines in the brain of the lancelet, Branchiostoma lanceolatum. A fluorescence-histochemical and electron-microscopical investigation.

Authors:  H Obermüller-Wilén; T van Veen
Journal:  Cell Tissue Res       Date:  1981       Impact factor: 5.249

  7 in total

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