The distribution of substance P (SP) immunofluorescence was investigated in the Gasserian ganglion, ophthalmic nerve and in the anterior segment of the rabbit eye. About one third of the nerve cell bodies in the Gasserian ganglion exhibited SP immunofluorescence, which was also observed in some nerve fibres of the ophthalmic nerve. In the cornea, some SP-positive nerves were found in the stroma and few of them were also observed in the epithelium. The iris contained numerous nerve fibres with SP immunofluorescence. In the sphincter area such fibres were circular, while the orientation of the SP fibres was radial in the dilator muscle. Both in the iris and in the ciliar body, the largest vessels are surrounded by nerves exhibiting SP immunofluorescence. A few nerve fibres also appeared in the stroma of the ciliary processes.
Nerves showing acetylcholinesterase (AChE) activity or immunoreactivity for substance P (SP) were demonstrated in the human cornea. AChE-positive fibres were found in stromal nerve trunks from where they penetrated Bowman’s membrane and formed a basal epithelial plexus. Intraepithelial terminals arose from this network. SP immunoreactive nerve fibres showed similar architecture but were fewer Both SP immunoreaction and histochemical AChE reaction were demonstrated consecutively in the same tissue section cut from both human and rabbit cornea. Stromal nerve trunks were found to contain SP immunoreactive and AChE-positive nerve fibres. However, the AChE-positive fibres were much more frequent than those immunoreactive for SP. In the rabbit Gasserian ganglion all neurons showed AChE activity but only some 20% were SP positive. It is concluded that all the sensory trigeminal nerve fibres of the cornea show AChE activity but only a proportion of them contain SP-like material.
Glomus cells from carotid bodies of adult rats dissociated by means of collagenase or collagenase + trypsin were used to study by electron microscopy the endocytotic uptake of cationized ferritin (CF) tracer into subcellular compartments. The glomus cells were incubated with the tracer (1) in a basic salt medium (BM), or (2) in the BM into which calcium ionophore A23187 had been added, or (3) in a potassium-rich medium. Incubation of the cells in BM containing CF for 30 min resulted in attachment of the tracer to the cell membrane and uptake of a few solitary tracer particles into small vesicles and multivesicular bodies. No uptake into the cisternae of the Golgi apparatus was observed. Further incubation in BM containing CF for another 30 min resulted in increased uptake of the tracer into small vesicles and multivesicular bodies. A similar pattern of uptake was observed when the dissociated glomus cells were first preincubated in BM with CF for 30 min and then incubated for 1 min or 30 min in the BM solution containing both the ionophore and CF. Upon such incubation, CF particles were seen to penetrate into coated pits and sites of exocytosis at the cell surface. When the 30-min preincubation in BM was followed by incubation in a CF-containing potassium-rich medium for 15-30 min, uptake into vesicles, small lysosomes and occasionally also into profiles of the smooth endoplasmic reticulum was seen. Endocytotic mechanisms of the glomus cells are outlined.
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