Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:3.2.1.36 (hyaluronidase)
 4,606 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A microcellular dispersion procedure for the rat neurohypophysis was developed, comprising tissue softening and dissociation using a special sieving sytringe. In preparatory studies the influence of mesh width, and treatment with trypsin, pronase or collagenase-hyaluronidase was investigated using light and electron microscopy, as well as with microchemistry by means of protein and lactate dehydrogenase activity determinations. Trypsinization gave the best results. In the final adopted procedure, 3 incubated neurohypophyses were sequentially sieved through a 200- and a 50-mum mesh. The resulting 50-mul dispersion was found to contain numerous ultrastructurally well-preserved pinched-off axonal endings (neurosecretosomes), and pituicytes often revealing processes. On the basis of DNA and oxytocin assays 11% of the pituicytes and 28% of the axonal cytoplasm were recovered. Oxytocin immunofluorescence microscopy showed hormone within the neurosecretosomes, but often also in the cytoplasm of pituicytes. Microdensity gradient centrifugation was performed on neurohypophyseal disperions, in order to obtain fractions enriched for neurosecretosomes and pituicytes. Fractions were characterized by means of phase contrast, oxytocin immunofluorescence and electron microscopy, as well as by oxytocin and DNA assays as respective markers. With a 10:14:22% (w/v) Ficoll gradient, fractions were obtained for which the relative purification was by a factor of 4 on the basis of DNA/oxytocin ratios.
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PMID:Enzymic preparation of neurosecretosome- and pituicyte-enriched fractions from the rat neurohypophysis. 18 63

Russian investigators have recently reported clinical recovery of enzyme treated, spinal cord transected rats. Using the exact protocols of Matinian and Andreasian's two most successful treatment regimens, we repeated their experiments using United States produced pure hyaluronidase and trypsin or trypsin and elastase. Animals were evaluated for return of bladder function, clinical evidence of hind limb motor function, cortical evoked response after sciatic nerve stimulation, and axonal transport of cortically injected tritiated proline by regenerated corticospinal axons. None of the treated animals differed from control animals treated only with the enzyme vehicle. No animals walked, had return of voluntary motor activity, showed cortical evoked response, or had evidence for transport of tritiated proline over regenerated corticospinal axons.
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PMID:Enzyme treatment of spinal cord transected rats. 42 86

The present review summarizes the outer and inner surface features of mossy fiber glomeruli in vertebrate cerebellar granular layer as seen by conventional scanning electron microscopy (SEM) and SEM freeze-fracture method. The intracortical trajectory of mossy fibers and their synaptic contacts with granule cell dendrites were traced by the slicing and freeze-fracture techniques revealing the radial distribution of granule cell dendrites around the central mossy rosette. The "en passant" nature of mossy fiber synaptic contacts and the participation of Golgi cell axonal ramifications were demonstrated. The results obtained were compared with available light and transmission electron microscopy data. The freeze-etching technique disclosed the true extension of glomerular neuroglial investment. The proteoglycan content of mossy fiber rosette has been also studied by Alcian Blue staining, enzymatic digestion with testicular hyaluronidase and neuraminidase and Os-DMEDA staining method resulting in the presence of an electron dense material at the mossy fiber axoplasmic matrix and some synaptic vesicles, pre-and postsynaptic densities and cleft substance. The axoplasmic material appears to be constituted by proteoglycans with hyaluronic acid or chondroitin sulphate in their composition. The possible role of proteoglycans in synaptic functions is also discussed. Scanning electron microscopy is a promising methodology for analysis of short intracortical circuits and for the study of complex multisynaptic arrangements.
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PMID:Three-dimensional morphology of cerebellar protoplasmic islands and proteoglycan content of mossy fiber glomerulus: a scanning and transmission electron microscope study. 194 30

Methods for the study of axons involve whole nerve preparations, teased preparations of axons that are excised from their proximal and distal connections, and tissue culture models. As a complement to these, it would be advantageous to study separated, isolated axons in vivo, still in continuity with the end organ distally and the spinal cord central nervous system neuron proximally. This would allow the study of axon function, normal or pathological, in a close relationship to its biological environment. To achieve this, we have passed the surgically isolated sciatic nerve of a rat through a chamber specially designed for enzymatic dissociation. This was based on principles derived from a prior in vitro method for dissociating nerve into axons. The chamber has controlled temperature and flow and is on an inverted microscope stage, allowing observation of the process. We perfused the chamber with a calcium-free solution followed by a series of enzymes: collagenase, trypsin, and hyaluronidase. This dissociates that part of the extracellular matrix external to the Schwann cells, leaving free, myelinated axons with their Schwann cells. In this acute preparation, the axons continue to conduct action potentials for at least 8 hours. Furthermore, an in vitro study of the axon after the in vivo dissociation demonstrated that axonal transport was maintained in over 90% of the axons, directly visualized on an AVEC-DIC type of microscope system. Properties of axonal transport or active spike propagation can thus be studied individually in an in vivo axon preparation.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Model for the study of individual mammalian axons in vivo, with anatomical continuity and function maintained. 241 87

The stellate neurons of the cerebellar molecular layer have been mostly studied by light and transmission electron microscopy (TEM). However, the freeze-fracture scanning electron microscopy (SEM) and glycosaminoglycan histochemistry of these inhibitory microneurons have not been explored thus far. The freeze-etching technique, the freeze-fracture method for SEM and the conventional techniques for TEM were applied to cerebellar samples of Swiss albino mice and Arius spixii teleost fishes. In addition, Alcian Blue (AB) staining was applied to mouse cerebellar tissue in order to study glycosaminoglycan histochemistry. At the SEM level, the stellate neurons showed a short axonal plexus extending to the nearby secondary and tertiary Purkinje dendritic branches, and 2 to 4 conical dendrites receiving typical axo-dendritic synapses on their shafts. The fractured stellate neurons showed compact nuclear heterochromatin masses and the three dimensional interrelationship of ER and Golgi complex (Novikoff's GERL complex). The surface of the scarce endoplasmic reticulum was observed as strands extending from the nuclear envelope to the inner surface of the plasma membrane. At the TEM level, axosomatic endings of parallel and climbing fibers were distinguished. The cytochemical study revealed a homogeneous alcianophylic cytoplasmic substance, sensitive to hyaluronidase. This was particularly evident around and within the nucleus. The AB results indicated the presence of hyaluronic acid. A complex neuropil formed by Purkinje cell spiny branches, bundles of parallel fibers, spine synapses and Bergmann astrocytic cytoplasm was seen adjacent to the stellate neurons.
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PMID:Electron microscopy and glycosaminoglycan histochemistry of cerebellar stellate neurons. 361 65

(1) Block of conduction and marked increase in permeability of the squid giant axon, when surrounded by adhering small nerve fibers, is caused by the venoms of cottonmouth, ringhals, and cobra snakes and by phospholipase A (PhA). This phenomenon is associated with a marked breakdown of the substructure of the Schwann sheath into masses of cytoplasmic globules. Low concentrations of these agents which render the axons sensitive to curare cause less marked changes in the structure of the sheath. (2) Rattlesnake venom, the direct lytic factor obtained from ringhals venom, and hyaluronidase caused few observable changes in structure, correlating with the inability of these agents to increase permeability. (3) Cottonmouth venom did not alter the structure of giant axons freed of all adhering small nerve fibers. This is in agreement with previous evidence that the venom effects are due to an action of lysophosphatides liberated as a result of PhA action. Cetyltrimethylammonium chloride, a cationic detergent, produces effects that resemble those of venom and PhA. (4) The results provide evidence that PhA is the component of the venoms that is responsible for their effects. It also appears that the Schwann cell and possibly the axonal membrane are the major permeability barriers in the squid giant axon.
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PMID:Fine structural alterations associated with venom action on squid giant nerve fibers. 417 May 46

Histopathological changes in the retina and optic nerve in imperfect albino mutant quails with a sex-linked recessive gene were studied ontogenetically. The mutant quail showed eye enlargement 3 months after hatching. The eyes exhibited hazy corneas, lens opacities and deep anterior chambers at 18 months of age. Some ganglion cells in the retina and axons in the optic disc began to degenerate 6 months after hatching. There were many deformed or fragmented ganglion cells at 12 months of age, and axonal degeneration was observed in the optic disc. The optic disc and the retina around it became excavated. At this time, hydropic degeneration was found in the ganglion nerve fibre layer and optic nerve and a small accumulation of acid mucopolysaccharide, which was sensitive to hyaluronidase, was present in the optic disc and optic nerve. The excavation was found to be fully developed around the optic disc at 18 months and most ganglion cells showed degenerative changes. During this period, the inner plexiform and inner nuclear layers showed hydropic degeneration. At 24 months the ganglion cell and ganglion nerve fibre layers had disappeared, the thickness of the inner nuclear layer was reduced and many photoreceptor cells were totally degenerated. The optic nerve was occupied by glial cells, blood vessels and cavernous spaces in which acid mucopolysaccharide accumulated. These histopathological retinal changes in the mutant quail are very similar to those reported in experimentally induced glaucoma of other animal species and to those in human glaucoma. The usefulness of this mutant quail as an animal model for the human disease is discussed.
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PMID:Histopathological changes of the retina and optic nerve in the albino mutant quail (Coturnix coturnix japonica). 647 Feb 27

The binding of cholera and tetanus toxins to receptors on the surfaces of teased nerve fibers was used to localize GM1 and G1b-series gangliosides, respectively, by immunocytochemical methods. Native fibers and fibers treated with various hydrolytic enzymes to degrade specific surface components were studied. With native fibers, both toxins bound abundantly to nodes of Ranvier and poorly to the most external, internodal Schwann cell surfaces. Treatment of the fibers with proteases, hyaluronidase, and chondroitin ABC lyase neither eliminated receptors at the nodes nor unmasked receptors over the internodes. The axolemma underlying the paranodal or internodal myelin, exposed by extensive treatment with protease, bound both toxins in large amounts. Neuraminidase action induced cholera toxin receptors on the Schwann cell surface; these receptors were insensitive to protease. The results indicate that GM1 and G1b-series gangliosides are predominantly localized to axonal and glial structures of the node of Ranvier and to paranodal/internodal Axolemma, and that polysialogangliosides not of the G1b-series are present on the internodal Schwann cell surface.
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PMID:Differential expression of gangliosides on the surfaces of myelinated nerve fibers. 650 52

Anionic sites in the rat sciatic nerve were studied by light and electron microscopy using a fine-granular cationic colloidal iron staining method (Murakami et al., 1986). The axon, as well as the endoneurium, the epineurium and the basement membrane of Schwann cells, were all confirmed to react strongly to the cationic colloidal iron even at a pH value of 1.0-2.0. Prior hyaluronidase digestion decreased the colloidal strain of the epineurium; chondroitinase ABC weakened that of the endoneurium and the basement membrane of Schwann cells. However, as axons retained stainability with cationic colloidal iron even after combined digestion with hyaluronidase, chondroitinase ABC, heparitinase and keratanase, the authors consider sulfated glycoconjugates and not those substances which are digestible with such common enzymes. The acid groups ionized at pH 1.0 are most likely sulfate groups. Methylation deprived the axon of the reactivity to cationic colloidal iron staining, and even subsequent saponification could not recover this reactivity to its full extent. In the axon, electron microscopy revealed a deposition of colloidal iron on the external surfaces of microtubules and neurofilaments in the axoplasm and of very fine filaments connecting them. This highly negatively charged intra-axonal network could also serve toward a supportive function in maintaining the spatial distribution of microtubules either mechanically or through electrostatic repulsion or, possibly, serve as an intra-axona cation exchange reservoir.
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PMID:Strongly anionic sites in peripheral axons of the rat sciatic nerve: light and electron microscopic detection using cationic colloidal iron. 856 39

The glycosaminoglycans of sciatic nerves recovering from crush-injury were studied in adult guinea pigs and compared with those of non-injured mature neural tissues. The glycosaminoglycans were recovered from the 1,900 g supernatant and pellet of the tissue homogenates and assayed for hexuronate contents and susceptibilities to hyaluronidase, chondroitinase ABC, and nitrous acid. In the normal brain and central nerve tracts, the glycosaminoglycans were distributed both in the supernatant and pellet fractions; the brain showed a predominance of chondroitin sulphates but the tracts showed a predominance of heparan sulphates. Twice as much glycosaminoglycans were found in normal sciatic nerves, only in the pellet fraction and with heparan sulphate predominant. In the 2 weeks post-crush, progressive increase in hexuronate was observed, due mainly to additional chondroitin sulphate forms in the supernatant; the pellet fraction in the same period was however similar to the untreated controls in relative abundance of glycosaminoglycan classes and hexuronate content. At 4 weeks post-crush, although the total hexuronate returned to the control level, a significant proportion of glycosaminoglycans remained in the supernatant fraction. Evidence is thus provided for the need to modulate the glycosaminoglycan expression pattern in adult neural tissue to allow post-traumatic tissue remodelling and axonal regrowth.
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PMID:Changes in glycosaminoglycans during regeneration of post-crush sciatic nerves of adult guinea pigs. 895 Jul 6


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