Electron microscopic study of the porcine choroid plexus epithelium

The choroid plexus (CP) is a highly vascularized organ in the brain ventricles which acts as the main producer of cerebrospinal fluid (CSF). A study of the surface ultrastructure of the porcine CP was performed using scanning and transmission electron microscopy. The vascular walls of the capillaries were fenestrated. Epiplexus cells of different morphology were abundant on top of the epithelial surface. Two types of epithelial cells were present, characterized by the presence or absence of microvilli. Some epithelial cells contained cilia while other cells had large secretory protrusions called blebs. In the choroid epithelium of the lateral ventricles, some cells with large depressions were present. Cells with peduncles, such as recently discovered in the buffalo, could not be recognized. The variability of the choroidal surface structures clearly indicates the active role of the CP in the formation and maintenance of the CSF and its components.     

Das Blutgefäßsystem des Enddarms vom Hund (Canis lupus f. familiaris)

The Vascular System in the Large Intestine of Dog (Canis lupus f. familiaris) The vascular System of the large intestine of 10 dogs was examined by means of vascular corrosion casts, histology and transmission-electron microscopy. The tela submucosa contains an arterial and a venous vascular plexus. In broader areas of the submucosa, a deep and a superficial vascular plexus, which are interconnected, can be found. The plexus are orientated parallel to the layers of the intestinal wall. On the one hand, these vessels naturally provide self-sufficiency and drainage of the submucosa, and, moreover, direct branches to the stratum circulare of the muscular layer. On the other hand, the submucosal vascular plexus is the ‘distributional network’ for the functional plexus of the tunica mucosa. The arteries, which ascend to the tunica mucosa, supply a flat arterial network underneath the intestinal glands. Bundles of only a few arteriolae originate from this in order to supply the pericryptal capillaries. In the vicinity of the cryptai orifices, these turn into a network of subepithelial capillaries, which is post-connected to the periglandular capillary plexus. From this ‘terminal circulatory pathway’, the blood is drained off by veins that enter the submucosal plexus. It is characteristic that the postcapillary venules often begin as part of the capillary network. As in other species, the subepithelial capillaries are predominantly lined with a ‘fenestrated endothelium’, whereas the capillaries of the pericryptal areas show a continuous endothelium. The latter contains multiple vesicles that may fuse in order to form transcytoplasmic channels as a morphological equivalent for transcappillar-epithelial and vice versa occurring transport of substances.     

Über die intramuralen Blutgefäße des Enddarms vom Pferd (Equus przewalskii f. caballus)

The vascular system of the large intestine of 12 horses was examined by means of vascular corrosion casts, histology and transmission electron microscopy providing the following results. The Aa. et Vv. breves et longae leave the mesenteric vessels, respectively the subserously on the teniae lying cecal vessels to reach the tela subserosa at the mesenteric margin. The short vessels enter the deeper layers of the wall instantly, whereas the Aa. et Vv. longae move towards the submucosa by penetrating the muscular layers after a variable subserous course. The tela submucosa contains an arterial and a venous vascular plexus. In broader areas of the submucosa a three-dimensional vascular network can be found. This consists of a deep and a superficial vascular plexus, which are closely interconnected. The deep plexus is applied to the inner circular muscles, whereas the superficial plexus is adjacent to the muscularis mucosae. The (deep) arterial plexus receives its afflux from the Aa. breves et longae and supplies parts of the circular muscle layer with recurrent muscle branches. The vascularisation of the mucosa also originates from the submucosal (superficial) plexus. In the basal tunica mucosa, the ascending arteries form a transversal network from which arterioles branch into periglandular capillaries around each Lieberkühn crypt. Close to the lumen, a polygonal subepithelial capillary system is formed. The capillaries turn into postcapillary venules immediately below the epithelium of the mucosal surface. Veins move vertically through the submucosa to enter the submucosal plexus after few inflowing side branches. Branches of the subserous-submucosal connections form an intermuscular plexus between the circular and longitudinal muscular layer. This plexus supplies the capillaries of the tunica muscularis. The subepithelial capillaries are predominantly lined with a fenestrated endothelium, whereas the capillaries of the pericryptal mucosa mainly show a continuous endothelial lining. The latter contain multiple vesicles, which may fuse in order to form transcytoplasmic channels. Sphincter-like muscle bundles at the transition points from capillaries to venules may provide hemodynamic regulatory structures in the submucosa of the horse. Veins with circumferential cushions of smooth muscle fibres, so-called ‘throttle veins’, are also found.     

Das Blutgefäßsystem des Enddarms vom Schwein (Sus scrofa f. domestica)

The circulatory system of the large intestine of 27 pigs was examined by means of corrosion anatomy (vascular casts), histology and electron microscopy. The results were as follows: The Aa. et Vv. breves et longae leave the mesenteric vessels and reach the wall of the intestine at the mesenteric margin. The short vessels enter the deeper layers of the wall, whereas the Aa. et Vv. longae, by taking a variable subserous course, reach the submucosa af ter penetrating the muscular layers. The tela submucosa contains an arterial and a venous vascular plexus. Where the submucosa is larger, there is a three-dimensional vascular network, a deep and superficial vascular plexus that are closely interconnected. The deep plexus is applied to the inner circular muscles, whereas the superficial plexus is adjacent to the muscularis mucosae. The deep arterial plexus receives its af flux from the Aa. breves et longae and provides part of the circular muscle layers with recurrent muscle branches. The vascularization of the mucosa is derived from the (superficial) submucosal plexus. The arteries that ascend the tunica mucosa ramify, in the form of a brush, into some arterioles. In the basal part of the mucosa, they turn into a periglandular capillary system, i.e. a network around each Lieberkühn crypt. Close to the lumen, a polygonal subepithelial capillary system is formed. Below the epithelium of the mucosal surf ace, the capillaries turn into postcapillary venules. These are running vertically through the submucosa, with few infiowing side branches, and finally enter the submucosal plexus. An intermuscular plexus is formed by anastomoses between the circular and the longitudinal muscular layers from the branches of the subserous-submucosal connections. This intermuscular plexus provides the capillaries for the tunica muscularis. The subepithelial capillaries are, above all, furnished with a so-called fenestrated endothelium, whereas the capillaries of the pericryptal mucosa mainly show a continuous endothelium. The latter contains multiple vesicles that can fuse to form transcytoplasmic channels. In the wall of the large intestine of the pig, there are no sure indications as to the existence of either arterio-venous anastomoses or haemodynamic regulatory structures.     

A histologic and immunocytochemical study of choroid plexus tumors of the dog

Sixteen choroid plexus (CP) tumors in 12 male and four female adult dogs were analyzed microscopically. Tumors were in the lateral (six), third (six), and fourth (four) ventricles. The average age of the dogs was 6 years. Tumors were classified by the following criteria: 1) choroid plexus papilloma (CPP), which resembled normal choroid plexus and had low mitotic activity; 2) choroid plexus papilloma (CPP), which resembled normal choroid plexus and had low mitotic activity; 2) choroid plexus papilloma with atypical features (atypical CPP), which had increased cellular density, nuclear atypia, two to four mitoses per 40x microscopic field, necrosis, and infiltration of the brain parenchyma and/or leptomeninges; and 3) choroid plexus carcinoma (CPC), which had marked nuclear atypia, poorly formed papillae, greater than four mitoses per 40x microscopic field, abnormal mitotic figures, and/or extraneural metastasis. The 16 tumors were classified either as CPP or atypical CPP (none as CPC). Statistically significant associations between brain infiltration and necrosis and atypical CPP were identified. Immunohistochemical studies in 11 tumors demonstrated staining for keratin in three tumors, two of which also reacted with carcinoembryonic antigen (CEA). There was no immunoreactivity with glial fibrillary acidic protein or epithelial membrane antigen. Choroid plexus from one of three control dogs stained focally for cytokeratin only. It is concluded that normal choroid plexus and CP tumors in the dog express epithelial, but not glial differentiation.     

Scanning electron microscopy of the choroid plexus of the lateral ventricle of the horse

The present study examined the ultrastructure of the choroid plexus of the lateral ventricle of the horse. The material was fixed in 2.5% glutaraldehyde in 0.1 m sodium phosphate buffer, pH 7.3, processed and analysed by scanning electron microscopy. The choroid plexus was characterized by regions with a predominance of villi, which resembled finger-like projections or bunches of grapes, and others where straight and uniform folds predominated. Epithelial cells projected into the ventricle and large amounts of cilia and microvilli were observed on their surface. The choroid glomus corresponded to a dilatation of the choroid plexus and was characterized by blood vessels of different calibres surrounded by connective tissue.     

Isolation of visna-maedi virus from the choroid plexus of an apparently healthy sheep in Italy

In this paper, the presence of visna-maedi in Italy, reported to exist since 1982 on clinical grounds, and the presence of anti-visna-maedi antibody is confirmed by the isolation of the viral agent from choroid plexus cells of an apparently healthy sheep. Gel diffusion test antigen, prepared from the explanted choroid plexus cells and from normal choroid plexus cells infected with the isolated agent, gave a positive reaction with one or two identity lines with reference antigens. The isolated agent gave both a characteristic cytopathic effect and a cytoplasmic fluorescence starting 24 hours after infection in normal choroid plexus cell cultures. Fluorescence was observed neither in control normal choroid plexus cells nor in infected normal choroid plexus cells incubated with a visna-maedi negative serum. By electron microscopy, budding forms arising from the cell membrane and extracellular particles of two distinct types were observed. One type was characterized by an electron-dense central core and a single membrane, and ranged from 80 to 110 nm, while the other had elongated bar-like cores and a double wall, and ranged from 100 to 140 nm. The characteristics observed for the isolated agent are identical to those reported by various authors for visna-maedi virus.     

Isolation of visna-maedi virus from the choroid plexus of an apparently healthy sheep in Italy

In this paper, the presence of visna-maedi in Italy, reported to exist since 1982 on clinical grounds, and the presence of anti-visna-maedi antibody is confirmed by the isolation of the viral agent from choroid plexus cells of an apparently healthy sheep.Gel diffusion test antigen, prepared from the explanted choroid plexus cells and from normal choroid plexus cells infected with the isolated agent, gave a positive reaction with one or two identity lines with reference antigens. The isolated agent gave both a characteristic cytopathic effect and a cytoplasmic fluorescence starting 24 hours after infection in normal choroid plexus cell cultures.Fluorescence was observed neither in control normal choroid plexus cells nor in infected normal choroid plexus cells incubated with a visna-maedi negative serum.By electron microscopy, budding forms arising from the cell membrane and extracellular particles of two distinct types were observed. One type was characterized by an electron-dense central core and a single membrane, and ranged from 80 to 110 nm, while the other had elongated bar-like cores and a double wall, and ranged from 100 to 140 nm. The characteristics observed for the isolated agent are identical to those reported by various authors for visna-maedi virus.     

Microvasculature of the hamster eye: scanning electron microscopy of vascular corrosion casts

The architecture of the retina, choroid and anterior eye segment was investigated in 12 Syrian hamsters using scanning electron micrographs of methylmethacrylate corrosion casts. The hamster eye receives its primary blood supply from the long posterior ciliary artery, which directly enters the optic nerve head, and divides into three branches: the central retinal artery and medial and lateral long posterior ciliary arteries. In the retina the central retinal artery divides into six radiating branches. Retinal arterioles form a slender and long course to capillaries. Retinal capillaries are extremely thin in diameter and form a sparse capillary network. The choroid is supplied by the long posterior ciliary arteries. Choroidal arterioles exhibit a thick and short course to the choriocapillaris. The choriocapillaris is thick and sinusoid-like, forming a dense network in the choroid. The ciliary body, iris and bulbar conjunctiva are supplied by the anterior ciliary arteries, which are branches of the long posterior ciliary arteries. Capillaries supplying the anterior margin of the ciliary process are large in diameter with an irregular bore, forming a thoroughfare channel draining blood in the ciliary arterioles into the pars plana vessels. Blood from the retina is drained by the central retinal veins. Venules from the anterior eye segment empty into the vortex veins via the pars plana vessels. Venous blood from the choroid is drained only by vortex veins via the choroidal veins. The functional significance of the vascular architecture and species differences are discussed.     

Microvasculature of the rat eye: scanning electron microscopy of vascular corrosion casts

Methylmethacrylate castings of the eye microvasculature were prepared from 10 Spargue-Dawley rats and studied by electron microscopy. The choroidal arterioles are larger in diameter than retinal arterioles, and have a shorter course to choroidal capillaries than retinal arterioles to retinal capillaries. Retinal capillaries are extremely thin in diameter and form a sparse retinal capillary network. The choriocapillaris is large and sinusoid-like, forming a compactly arranged network in the choroid. These differences in the microvasculature between the choroid and retina help explain the differences in ocular hemodynamics; that is, the blood flow in the choroid is faster than that in the retina. Capillaries of the iris show a zigzag configuration, which may be an accommodation for dilation and constriction of the pupil. Capillaries of the ciliary body are of large diameter forming leaf-like configurations, presumably to contribute to the secretion of the aqueous humor. Capillaries of the conjunctiva exhibit a somewhat coiled configuration, the arrangement of which reduce tension of the conjunctiva vessels caused by eyeball movement. Intra-arterial cushions, which control blood flow at the branching sites, are found in both choroidal or retinal arterioles.     

Histopathologic and electron microscopic studies on the acute toxicity of ochratoxin A in rats

Ochratoxin A was given by gavage to male rats. Moribund and dead animals were necropsied, and the surviving rats, including the controls, were killed 48 hours after dosing. Many of the principal rats were moribund, or began dying, within 12 to 24 hours after dosing. Lesions suggestive of disseminated intravascular coagulation were seen by light microscopy as early as 12 hours after dosing; fibrin deposits were in the spleen, brain choroid plexus, glomerular capillaries, liver, and heart. Renal tubular nephrosis, hepatic and lymphoid necrosis, and necrotic enteritis with villous atrophy were also seen. Electron microscopy demonstrated fibrin strands mixed with degranulated platelets, necrotic leukocytes, and swollen endothelial cells in glomerular capillaries. Myocardial changes included focal supercontracted sarcomeres adjacent to intercalated disks. Swollen sarcolemma, lysed myofibrils and fragmented Z-bands with interstitial edema, vascular thrombosis, and endothelial damage were also seen. The acute pathologic changes induced by ochratoxin A in the intestine, liver, and lymphoid tissues were more obvious than the tubular nephrosis, and the development of a disseminated intravascular coagulation-like syndrome with myocardial changes was a complicating factor.     

A sacro‐caudal spinal cord choroid plexus papilloma in a shar‐pei dog

A seven‐year‐old shar‐pei dog was referred because of severe lumbosacral pain and faecal incontinence of 20 days’ duration. Neurological examination was characterised by plegic tail, absence of perineal reflex, dilated anus, perineum and tail analgesia, and severe lumbosacral pain. The neurological clinical signs were suggestive of a selective lesion involving sacral and caudal spinal cord segments and/or related nerve roots. A magnetic resonance imaging of lumbosacral spine was performed and was suggestive of an intradural lesion. Primary or secondary neoplasia was considered as the most probable differential diagnosis. The dog was euthanased upon the owner's request. Histopathological examination confirmed the presence of an intradural‐extramedullary neoplastic tissue enveloping intradural tract of spinal nerve roots. On the basis of histological and immunohistochemical findings, a diagnosis of well‐differentiated choroid plexus papilloma was made. To the authors's knowledge, this is the first case of primary or metastatic spinal choroid plexus papilloma in dogs.     

Magnetic resonance imaging in a dog with a choroid plexus carcinoma

Magnetic resonance imaging was used ante mortem to confirm the anatomic location of an intracranial lesion in a dog with neurological signs. Necropsy revealed the lesion to be a choroid plexus carcinoma with thalamic invasion. A review of the literature on choroid plexus carcinomas in the dog is included.     

Expression of cell adhesion molecules in canine choroid plexus tumors

Choroid plexus tumor (CPT) is a primary intracranial neoplasm of the choroid plexus epithelium in the central nervous system. In the current World Health Organization classification, CPT is classified into two categories; choroid plexus papilloma (CPP) and carcinoma (CPC). In the present study, we investigated immunohistochemical expressions of N-cadherin, E-cadherin and β-catenin in 5 canine CPT cases (1 disseminated CPC, 2 CPCs and 2 CPPs). One CPP case was positive for N-cadherin and β-catenin, but negative for E-cadherin. The disseminated CPC case was positive for E-cadherin and β-catenin, but negative for N-cadherin. The other cases were positive for the three molecules examined. These results suggest that loss of the N-cadherin expression might associate with the spreading of CPC cells.     

Microvascular architecture of the rabbit eye: a scanning electron microscopic study of vascular corrosion casts

The microvasculature of the eyes of 5 rabbits was investigated using scanning electron microscopy on corrosion casts. The study revealed that the pars plana vessels draining blood from the iris and ciliary body coursed directly into the anterior vortex venous system constituting the scleral venous plexus (the venous circle of Hovius). The episcleral vasculature was found to possess a specialized morphology, with channels draining the aqueous humor. The capillaries of the third palpebral, bulbar and palpebral conjunctiva formed a single-layered capillary network approximately parallel to the epithelium and formed a well-developed venous plexus in the stroma. The retina was found to be merangiotic, meaning that vessels were present only in a small part of the retina, extending in a horizontal direction to form bands on either side of the optic disc. Channels representing the aqueous veins that drained blood mixed with aqueous humor were found to derive directly from the suprachoroidal space and communicate with the scleral venous plexus via the anterior vortex veins. The functional significance of the microvasculature of the iris, cilia, retina and choroid is discussed in this report as well. The elaborate microvasculature of the conjunctiva may be a prerequisite for the exchange of nutrients and gasses between the cornea and the vessels across the conjunctival epithelium when the eyelids are shut during sleep, and possibly for the dynamics of eye drop delivery. The scleral venous plexus in rabbits may be analogous to the scleral venous sinus (Schlemm's canal) in rats, primates and humans.     

Prevalence of psammoma bodies in meninges and choroid plexuses of raccoons (Procyon lotor) from Parramore Island, Virginia.

Microscopic evidence of multifocal mineralizations (psammoma bodies) were seen in brains of 33/53 (62%) raccoons (Procyon lotor) necropsied on Parramore Island, Virginia. Most mineralized foci had concentric laminations and were present in small capillaries of meninges of the brain (15/33), in choroid plexus (3/33), or at both these sites (13/33). In 2 raccoons, the lesions were confined to the meninges of the proximal cervical spinal cord. In most cases, the affected vessels appeared to have been completely occluded. However, no evidence of ischemic changes in the brain parenchyma was seen, and none of the raccoons had abnormal neurologic signs prior to euthanasia. The condition appears to be a common incidental histopathologic finding in raccoons from the eastern United States. Although the exact cause of this condition is not known, a primary vascular insult with resultant dystrophic mineralization of the affected vessels is suspected.     

Microvascular anatomy of the pig eye: scanning electron microscopy of vascular corrosion casts

The microvasculature of the eye of 10 pigs was investigated using scanning electron micrographs of corrosion casts. The ciliary body, iris and bulbar conjunctiva were supplied by the iridociliary ring artery via the long posterior ciliary artery. Capillaries of the ciliary process were of large diameter (23.2-27.5 microm) with an irregular bore, forming a thoroughfare channel draining blood in the ciliary arterioles into the pars plana venous vessels. Arterioles and venules in the iris exhibited a zigzag or spiral features. The third palpebra was supplied by the anterior ciliary artery. The capillary bed of the third palpebra was dense and was formed by many rows of fine hair-pin loops. Capillaries in the bulbar conjunctiva formed a sparse network disposing approximately parallel to the epithelium and formed a well-developed venous plexus, draining into the vortex veins. Retinal arterioles formed a slender and long course to capillaries. Retinal capillaries were extremely thin (3.0-4.0 microm in diameter). The choroid was supplied by the short posterior ciliary arteries. Choroidal arterioles exhibited a thick and short course to the choriocapillaris. The choriocapillaris was flat and sinusoid-like (8.9-13.9 microm in diameter), forming a dense sheet-like network. Blood from the choroid emptied into the episcleral vein via the vortex vein. Blood from the retina was drained by the posterior ciliary veins. The functional significance of this vascular architecture was discussed.     

One-cycle growth studies with Maedi—Progressive pneumonia—Visna viruses: Shorter latent periods revealed

The latent periods of Visna virus and of progressive pneumonia virus were demonstrated by one-cycle growth studies to end 14–16 hr after infection of sheep choroid plexus cell cultures. Maedi virus was demonstrated to have a 14–18-hr latent period.