PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “EPENDYMA”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 163 records · Page 9Linked to original sources

Fetal antigen retained by mature neurons and ependyma studied with a monoclonal antibody (6B9).

A mouse monoclonal antibody (MAb 6B9, isotype IgM) was raised against autopsy tissue samples from the central nervous system (CNS) of multiple sclerosis (MS) patients. By immunofluorescence microscopy, MAb 6B9 intensely stains most or all cells in fetal rats. However, MAb 6B9 differentially stains various cell types in adult rats. Neurons, ependymal cells, and adrenal chromaffin cells are stained intensely, whereas astrocytes and oligodendrocytes are not stained. The 6B9-reactive antigen (6B9 antigen) is sensitive to periodic acid, but insensitive to treatment with protease, RNase, or hyaluronidase. Results from immunofluorescence microscopy on semithin sections and cultured neuroblastoma cells indicate that 6B9 antigen is intracellular. This is supported by immunoelectron microscopy, where labeling for 6B9 antigen appears in the cytoplasm distinct from any identifiable organelle. Further studies on 6B9 antigen should reveal its chemical nature as well as the significance of developmental changes in its distribution.

Animals↗

Ependyma and meninges of the spinal cord of the mouse. A light-and electron-microscopic study.

In addition to ependymal epithelial cells, numerous tanycytes are found along the entire central canal of the mouse. These tanycytes are arranged in clusters in the cervical, thoracic and lumbar segments of the spinal cord. In the conus medullaris, tanycytes separate and ensheath bundles of myelinated and unmyelinated axons; their processes take part in the formation of the stratum marginale gliae. In the caudal part of the spinal cord, the ventral wall of the central canal is thin and some areas are reduced to a single-cell thickness. In this region, ependymal cells participate directly in the formation of the stratum marginale gliae. The meninges consist of the intima piae, the pia mater, the arachnoid, a subdural neurothelium and the dura mater. The subarachnoid space appears occluded and opens only around the spinal roots. In the vicinity of the spinal ganglia, the dura mater, the subdural neurothelium and the arachnoid form a cellular reticulum.

Animals↗

Localization of immunoreactive prolactin in ependyma and circumventricular organs of rat brain.

Immunoreactive prolactin (IMP) has been localized in the male rat brain using the soluble peroxidase-anti-peroxidase (PAP) technique. In normal untreated animals, reaction product was seen in choroid plexus (CP) and in ependymal cells of the ventricular lining with heaviest concentrations of positively staining cells in the 3rd ventricle near the subcommissural organ (SCO), in the lateral ventricles near the subfornical organ (SFO), and in the 4th ventricle near the area postrema (AP). IMP was also present in numerous ependymal cells resembling tanycytes in the cerebral aqueduct, central canal of the spinal cord at the level of the AP, the organum vasculosum of the lamina terminalis (OVLT) and the floor of the infundibular recess. Immunoreactive cells resembling neurons were localized within the substance of the AP, SCO, and OVLT. IMP was also present in fibers of the zona externa of the median eminence and infundibular stalk; a few cells of the pars tuberalis contained reaction product. Hypophysectomized rats and bromocriptine-treated rats exhibited a similar staining pattern except that bromocriptine treatment eliminated IMP from most CP cells. Hypophysectomy, bromocriptine or estrogen treatment enhanced staining for IMP in cells of the pars tuberalis; estrogen treatment or hypophysectomy produced an increase in the number and distribution of immunoreactive cells as well as increased density of reaction product in cells of the medial habenular nucleus. The functional relevance of prolactin in these locations in the brain, the possible routes of transport of prolactin from the pituitary gland to the central nervous system, and the strong suggestion of extra-pituitary sites of synthesis of a prolactin-like hormone are discussed.

Animals↗

Morphological evidence for the presence of two cell types in the ependyma of the subcommissural organ of the snake, Natrix maura.

Two different types of ependymal cells were found in the subcommissural organ (SCO) of Natrix maura. Most secretory cells showed morphological features resembling the general structure and ultrastructure of cells in the SCO of other vertebrates. This report describes a second population of cells lining a portion of the dorsal groove of the SCO. These cells were not selectively stained by chromalum-hematoxylin and, under the electron microscope, they were characterized by scarce surface differentiations, sparse apical cytoplasm and short basal processes. Flat, parallel cisternae of the rough endoplasmic reticulum produced vesicles that appeared to be transported to the well-developed Golgi apparatus. Dense secretory granules about 200 nm in diameter were found in the Golgi region. Similar granules were seen in the vicinity of the apical plasma membrane; some of them opened toward the ventricle. All these characteristics clearly differentiate this cell group from the other secretory cells lining the SCO laterally and ventrally.

Animals↗

Specialized ependyma in the posterior mesencephalon of the chicken: the fine structure of the subtrochlear organ.

A formation of specialized ependymal cells in the posterior mesencephalon of the domestic fowl, designated as the subtrochlear organ, was examined with light-, scanning- and transmission electron microscopy. This organ possessing the form of the letter "V" is located in the ventricular wall of the posterior mesencephalon. Its apex marks the median sulcus, while the arms of the V are directed rostrolaterally. Ependymal cells lining the subtrochlear organ usually project an extremely elongated process into the subependymal region and are classified into three types according to their surface features: (1) cells with a bulb-shaped protrusion that projects into the ventricle, (2) single cilium-bearing cells, and (3) cells with a tuft of cilia. The first type of cell is restricted to the median portion of the subtrochlear organ; its bulb-shaped protrusion contains numerous ribosomes. The second type of cell predominates in the arm (rostrolateral) area; in its apical cytoplasm such ciliary structures as basal body are rarely seen. The third type of cell is usually assembled into several small islands on the arm area; it has many basal bodies and other ciliary structures in the apical cytoplasm.

Animals↗

The ependyma on the pineal of the Guinea pig (Cavia cobaya). A scanning electron microscopic investigation.

The proximal part of the epiphysis cerebri of the guinea pig is in close contact with the cerebrosopinal fluid of the third ventricle. A direct contact is not present as the pineal tissue is covered by a continuous ependymal layer. Two types of ependymal cells with different surface protrusions are discussed as being involved in possible interactions between the neuroendocrine tissue of the pineal organ and the cerebrospinal fluid. In addition, two different types of supraependymal structures are found on the ependymal surface of the habenulae and the wall of the third ventricle. Because of their morphological characteristics, these supraependymal structures are thought to be neural elements.

Animals↗

Changes of ventricular ependyma and choroid plexus in experimental hydrocephalus, as observed by scanning electron microscopy.

Hydrocephalus was induced in rats by the injection of silicone oil or kaolin suspension into the cisterna magna. One to 5 weeks later the walls of the lateral ventricles were studied with the scanning electron microscope after killing the animals by perfusion fixation. In contrast to controls, the hydrocephalic animals killed 1 or 2 weeks after injection showed degeneration of ependymal cilia and infestation of the ependymal and choroid plexus surface with reactive cells, which presumably may be identified as Kolmer phagocytic cells by their ultrastructural features as studied by the transmission electron microscope. A coating of debris on the surface of the choroid plexus in the hydrocephalic animals possibly bears upon the ciliary degeneration with consequent deficiency of the clearing effect of ciliary movement. In the longer surviving hydrocephalic animals regeneration of cilia seemed to have occurred.

Animals↗

New ultrastructural changes of the ependyma in experimental hydrocephalus.

New ultrastructural alterations of the ependymal cells in the altered container model of experimental feline hydrocephalus are described. These include half desmosomes and a basal lamina on the apical surface of the ependymal cells, punctate adhesion-like structures between intraventricular mononuclear cells and the apical surface of the ependymal cells and unusual distortion of the ependymal cells. The significance of these previously unreported morphological alterations is unknown.

Animals↗

Post-mortem modifications of the ependyma of the lateral ventricular wall.

The ependymal lining of the lateral ventricles of the brain of rats, rabbits, and man was investigated at several times after death. In contrast to control material that was fixed by the aldehyde perfusing method, the following post-mortem (p.m.) changes were found: (1) Cytoplasmic protrusions of ependymal cells appear 15 min p.m. They are present up to several hours after death. (2) The formation of these protrusions causes the tufts of cilia to clump together and later to become integrated within the ependymal cell. This may simulate an unciliated surface. (3) Small porelike holes, which are present 15 min p.m. in the ependymal cell membrane, enlarge and in later stages produce a meshwork of fibers instead of a closed ependymal lining. (4) TEM observation shows that ependymal cells are separated from each other very soon after death by intercellular gaps. Cell junctions between ependymal cells resist separation over a longer p.m. period. In animal or human material that is fixed at any time after death, such modifications have to be considered very critically. In human p.m. autopsy material they are mostly the expression of a p.m. alteration.

Animals↗

The fine structure of stratified ependyma in the ventricular wall of N-ethyl-N-nitrosourea-treated rats.

Ependymal stratifications, up to 15 cell layers in thickness at the floor of the lateral ventricle of rats treated transplacentally with N-ethyl-N-nitrosourea (ENU), are described. Ultrastructurally the constituent ependymal cells are well-differentiated and show no morphological signs of neoplasia. The possibility that these findings are due to the toxicity or carcinogenicity of ENU is discussed.

Animals↗