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)

From examination of the structural data obtained for the tongue of rodent Jaculus jaculus, it has been possible to deduce that it is lined with filiform papillae in the dorsal epithelium and that it has a rich glandular apparatus consisting of anterior serous glands which are located immediately after the apex and composed of epithelial cells arranged in a single synctitial layer, and both nucous and seromucous acini (Weber's glands) in the posterior portion of the tongue on the lateral sides and ventromedian region respectively. In the tip glands there is an elaboration of protein material; both neutral and acid glycoproteins are absent. In the posterior Weber's glands acidic moieties in the mucosubstances are due mainly to sialomucins and hyaluronidase resistant sulfomucins; in the seromucous acini on the other hand, mucopolysaccharides with vicinal hydroxyl groups and proteins are present. The histoenzymological tests employed to detect the succinic dehydrogenase and carbonic anhydrase also revealed the two reactions in the seromucous acini. Their presence is discussed on the basis of their having a probable role in the salivary production mechanisms in the same way as those cells which have a very strong secretory activity, or those involved in ionic reabsorption processes. The role of granular catalase activity in the duct cells is assumed to be able of protecting the glandular parenchyma from bacterial attacks. The presence also of acid glycoproteins within the lingual glands is correlated with taste sensation in view of the current revaluation of the role played by the proteoglycans in neuronal functions.
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PMID:Histochemical distribution of acid mucopolysaccharides and some active transport enzymes in the lingual glands of Jaculus jaculus L. (Dipodidae, Mammalia). 9 83

Plasma membranes of boar sperm from caput, corpus and cauda of the epididymis were purified by differential- and sucrose-density equilibrium centrifugation and were found to yield a single band at a density of 1.13 g/cm3. This fraction was enriched in acid and alkaline phosphatase, 5'-nucleotidase and (Na+ + K+)-ATPase activities, whereas it contained minimal amounts of hyaluronidase and N-acetylglucosaminidase and no succinic acid dehydrogenase activities. The plasma membrane of caput, corpus and cauda sperm had the same phospholipid/protein and cholesterol/phospholipid ratios but yielded different amounts of protein and individual lipid classes. Several changes in the plasma membrane were observed during transit of sperm through the epididymis. Within the phospholipid class a decrease in the percentage of phosphatidylethanolamine, phosphatidylserine and phosphatidylinositol was detected accompanied by an increase in amount of phosphatidylcholine, sphingomyelin and polyphosphoinositides. In the other lipid classes there was a decrease in the amount of free fatty acid and the major glycolipid. The amount of cholesterol decreased, while the amount of desmosterol and cholesterol sulfate increased. There was an increase in the amount of diacylglycerol. In addition, the changes in the fatty acid composition of the total membrane lipid and each phospholipid were determined. The above changes in the lipid composition of the plasma membrane during epididymal maturation may help to explain the decreased resistance to cold shock and changes in membrane fluidity of sperm during transit in the epididymis.
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PMID:Changes in the lipid content of boar sperm plasma membranes during epididymal maturation. 399 37

Our aim was to develop a fibroblast-free monolayer culture of human gastric mucosal cells, using the specimens obtained by routine endoscopic biopsy. Human gastric mucosa obtained from normal volunteers by endoscopic biopsy was dissociated from collagenase and hyaluronidase. Dissociated cells were cultured in supplemented Coon's modified Ham's F-12 medium. Within 24 hr of inoculation, the cells were attached to the culture dishes. This was followed by cellular outgrowth. On phase-contrast microscopy, all cells had epithelial characteristics and fibroblasts were not observed. Ninety percent of cells contained periodic acid Schiff reaction-positive mucous granules after diastase digestion consistent with mucous epithelial cells. Two percent of the cells gave a strong reaction for succinic dehydrogenase activity (parietal cells). Immunohistochemical staining for pepsinogen in cultured cells was negative. On EM, microvilli-like projections, junctional complexes, Golgi apparatus, and mucous granules were apparent in the majority of cells. Mitotic figures were observed by day 3 with Giemsa staining. Autoradiographically, these cells were able to incorporate [3H]TdR into the nuclei. Cells were capable of synthesizing DNA, and this function was inhibited by cycloheximide. Cells could be cultured for up to two weeks without fibroblast contamination. A method of primary monolayer culture of human gastric mucosa obtained by a routine endoscopic biopsy has been successfully developed.
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PMID:A monolayer culture of human gastric epithelial cells. 686 89