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

Twenty-three cases of intramuscular myxoma were analyzed clinically and histologically. The mean age of the patients was 54 years, and two-thirds were women. Clinical follow-up of 2 to 17 years' duration revealed no recurrences or metastases. Intramuscular myxoma thus appears to be a completely benign tumor. One patient simultaneously had a myxoma in the muscle of the thigh and a lesion of fibrous dysplasia in the femur. In addition, 14 of 16 patients studied with x-ray had a significantly higher incidence of minor abnormalities in bones as compared with the normal population. The myxomas were characterized histologically by sparse cellularity, abundant intercellular material digestible with hyaluronidase, and lack of mitotic figures. At the ultrastructural level, the tumor cells showed characteristics of fibroblasts and myofibroblasts. Immunohistochemical analysis of intermediate filament proteins revealed vimentin- but no desmin-positivity in the tumor cells, and endothelial cell markers as well as S-100 protein were absent. This is compatible with fibroblastic-myofibroblastic nature of the myxoma cells.
Am J Clin Pathol 1985 Sep
PMID:Intramuscular myxoma--a clinicopathological study of twenty-three cases. 403 56

Chemical and histochemical analyses, including testicular and staphylococcal hyaluronidase digestion, have been made of a jaw myxoma and the results show the presence of two acid mucopolysaccharides. Of the total mucopolysaccharide present 80% was hyaluronic acid and 20% chondroitin sulphate. The high content of non-sulphated mucopolysaccharide would seem to explain the paucity of fibres characteristic of the myxoma. It is suggested that myxomas generally probably have a similar high hyaluronic acid content. It is considered that the cell concerned is a mesenchymal cell elaborating non-sulphated mucopolysaccharide and may be called a ;myxoblast'; it is metabolically different from the sulphated-mucopolysaccharide-collagen-producing fibroblast. The high hyaluronic acid content is much greater than that found in embryonic connective tissue and may be a significant factor in the neoplastic behaviour of the myxomatous tissue. The aggressive behaviour of the myxoma is against a simple reversion to embryonic mesenchyme. It is concluded that the myxoblast is an active mucopolysaccharide-secreting cell and that mucin in the myxoma is not a sign of cell degeneration of preexisting fibroblasts or collagen.
J Clin Pathol 1968 Sep
PMID:Chemical and histochemical characterization of mucopolysaccharides in a jaw myxoma. 423 75

Human whole saliva inhibited bacterial neuraminidases and the inhibition was found to reside in the salivary IgA fraction. Further, salivary immunoglobulin (Ig)A inhibited various bacterial enzymes and toxins: neuraminidases from Streptococcus mitis, Streptococcus sanguis, and Clostridium perfringens, hyaluronidase and chondroitin sulfatase from oral bacteria, diphtheria toxin, and streptolysin O. The inhibitory activity of salivary IgA did not correlate with that of serum on the basis of minimum inhibitory dose. A small amount of salivary IgA was required to inhibit oral bacterial neuraminidases, whereas a large amount was required to inhibit other bacterial neuraminidase. Therefore, it is concluded that the absence of neuraminidase activity of oral bacteria in whole saliva may be due to specific inhibition by salivary IgA.
Infect Immun 1973 Sep
PMID:Inhibition of enzymes by human salivary immunoglobulin A. 435 48

This literature review attempts to enumerate possible etiologies of postoperative peritoneal adhesions as well as to suggest preventitive measures. The theory that the cause of adhesions was development of fibrous tissue resulting from the destruction of serosa at surgery is discussed, but the author points out that numerous experimental and clinical experiences point to a more complicated etiology. Serosal defects do heal, and not necessarily through adhesion formation, as shown in experimental animals; therefore a new notion of the process of peritoneal repair was advanced which, simply stated, sees free-floating macrophages as the principal source of new serosa. So other areas and tissue types are probably the source of adhesions. The discussion of these other etiological factors include ischemic tissue as a source of adhesions and foreign body causes of granuloma and adhesions (primarily surgical glove powder). In terms of adhesion prevention, many approaches have been tried from using prophylactic agents to inhibit the formation of fibrin in peritoneal exudate (agents such as sodium citrate, heparin, and anticoagulants), use of enzymes and fibrinolytic agents, such as streptokinase and hyaluronidase, to introduction of inert polysiloxanes for prevention at the time of surgery. The use of cortisone, which has been reported to have good results, is also discussed. Finally, the control of distribution of adhesions by plicative techniques is enumerated. With the up-to-date knowledge that adhesions which develop after abdominal operations represent a vascular response by surrounding structures to the stimulus of ischemic tissue or foreign material within the peritoneal cavity, rather than a healing mechanism for serosal defects, a rational approach toward operating on adhesions is presented; this technique requires scrupulous surgical procedure, freedom from foreign body intrusion, the leaving open of serosal defects (rather than pulling together under tension), and, frequently, attempts to surgically ensure that the inevitable adhesion formation occurs in areas which are innocuous to adjacent structures.
Surg Gynecol Obstet 1971 Sep
PMID:The cause and prevention of postoperative intraperitoneal adhesions. 439 38

The lactic dehydrogenase agent was obtained in quantities sufficient for purification studies by growing the virus in Ehrlich ascites tumor-bearing mice. A rapid method of titration of the agent is described. Subsequent to the standard procedure of concentration of virus by treatment with hyaluronidase and centrifugation, lipids were removed by extraction with PE, without major loss of infectivity. Electron microscopic sections of purified preparations contained particles consisting of a dense inner ring of about 25 mmicro and a less dense ring extending to about 50 mmicro. The particles occur frequently in single-membraned vesicles of varying size, and occasionally in large double-membraned bodies. The purified LDH agent did not stimulate the formation of neutralizing antibodies in rabbits and guinea pigs. The crude LDH agent was found to be a low interferon producer. Increased interferon, produced by secondary inoculation with Newcastle disease virus temporarily decreased the titer of the LDH agent. The results of others regarding the nature and the size of the LDH agent are interpreted in regard to the findings presented, and the role of interferon in permanently LDH agent infected mice is discussed.
J Exp Med 1965 Sep 01
PMID:Some properties of the lactic dehydrogenase agent of mice. 584 May 39

1. Extracts of the cortex and the medulla of fresh kidneys from pigs, sheep and dogs were analysed for the presence of acid mucopolysaccharides.2. Acid mucopolysaccharides were found in the kidneys of the three species and were evenly distributed between cortex and medulla.3. The acid mucopolysaccharides isolated from either the medulla or the cortex of kidneys contained equal amounts of sulphated and nonsulphated fractions; these could be identified as chondroitin sulphate and hyaluronic acid, respectively.4. Urinary hyaluronidase was isolated from urine and estimated by means of turbidity measurements.5. Urine hyaluronidase depolymerizes the acid mucopolysaccharides extracted from either the cortex or the medulla of the kidneys from pig, sheep and dog.6. The enzymic activity of urine hyaluronidase could be expressed as units/mg of protein. The optimum pH activity of the enzyme is at about 4.0.
J Physiol 1966 Sep
PMID:The isolation of hyaluronic acid and chondroitin sulphate from kidneys and their reaction with urinary hyaluronidase. 591 46

1. The measured extracellular space of the taenia coli is large when small ions or molecules are used for the determination, and small when large molecules are used, even with identical experimental procedures.2. Extracellular hyaluronic acid has been detected histologically. It is apparently reduced by hyaluronidase.3. The extracellular inulin space increases after the tissue has been pretreated with hyaluronidase, although the ionic composition and wet weight are unchanged.4. It is suggested that the hyaluronic acid prevents the free entry of macromolecules such as inulin into the extracellular space by steric hindrance. Monatomic ions such as Na(+), Li(+), Cl(-), Ca(2+) therefore have a larger extracellular space available than is calculated on the basis of the inulin space.5. A slight shrinkage of the muscle cells can be detected when the incubation period is prolonged.
J Physiol 1966 Sep
PMID:The extracellular space of the smooth muscle of the guinea-pig taenia coli. 591 53

Parisi, Joseph T. (Duquesne University, Pittsburgh, Pa.). Significance of chromogenic variants in studies of virulence factors of Staphylococcus aureus. J. Bacteriol. 92:589-591. 1966.-Large numbers of chromogenic variants were isolated from cultures of a parent strain of Staphylococcus aureus growing in Brain Heart Infusion (Difco). The parent strain and four selected chromogenic variants were tested for either quantitative or qualitative differences in the production of extracellular substances associated with virulence. Quantitative differences were found in the ability of these strains to produce coagulase and hyaluronidase, whereas qualitative differences were found in the production of plate hemolysins, bound coagulase, opacity in an egg yolk medium, and a proteinase. In view of the rate and extent of the occurrence of these chromogenic variants, their presence in an inoculum could lead to inaccurate results in in vitro studies of staphylococcal virulence.
J Bacteriol 1966 Sep
PMID:Significance of chromogenic variants in studies of virulence factors of Staphylococcus aureus. 592 34

Paraffin sections from fifteen cases of malignant diffuse mesothelioma of the pleura and five cases of bronchial adenocarcinoma infiltrating the pleura were examined with an antiserum specific for factor VIII related antigen and with antisera against various epithelial markers: keratin, carcinoembryonic antigen (CEA), fat globule membrane antigen and secretory component. In all adenocarcinomas all the epithelial markers were present whereas the factor VIII related antigen was absent. The distribution of the fat globule membrane antigens, keratin, secretory component and factor VIII related antigen varied from one mesothelioma to another. The mesotheliomas were generally negative for CEA. The three mesotheliomas which were positive for CEA were also positive for alcian blue after hyaluronidase treatment. Amongst the markers used, CEA seems the most useful for the differential diagnosis between carcinoma and mesothelioma. However, the simultaneous detection of several markers allows the characterization of various phenotypes. Some of them are close to the phenotypes of true adenocarcinoma. A relation between a given phenotype and the biological behaviour of the tumour has still to be demonstrated.
Histopathology 1984 Sep
PMID:Immunohistological study of malignant diffuse mesotheliomas of the pleura. 608 69

Proteoglycans (PGs) are closely associated with cartilage calcification. We have examined the hypertrophic zone of rat epiphyseal cartilage, in which calcification is occurring, using the high-iron diamine-thiocarbohydrazide-silver proteinate (HID-TCH-SP) method for sulfated glycosaminoglycans, an immunoferritin method specific for chondroitin sulfate A, and the tannic acid-ferric chloride (TA-Fe) method to stain cartilage matrix granules (MGs) presumed to be PG monomers. HID-TCH-SP produced stain deposits with a diameter of 11.2 +/- 3.2 nm (mean +/- SD; n = 200) in the MGs. However, HID-TCH-SP staining was not discernible in membrane-limited matrix vesicles (MVs). In areas of advanced calcification, partially disrupted MVs and globular bodies (GBs), derived in part from disrupted and/or degenerated MVs, contained a few too many small HID-TCH-SP stain deposits. Further down the epiphyseal cartilage, intact MVs markedly decreased and the GBs, containing many small HID-TCH-SP stain deposits, significantly increased in number. These GBs were found exclusively in the longitudinal septa rather than in the transverse septa. After enzyme digestion with testicular hyaluronidase, small (7.2 +/- 1.2 nm in diameter) stain deposits remained in the MGs and GBs, presumably localized to keratan sulfate. Immunoferritin localizing chondroitin sulfate strongly stained MGs, whereas MVs and GBs lacked staining. TA-Fe staining of glycoconjugates in the GBs demonstrated a striking decrease in the diameter of MGs associated with calcification in the GBs as compared with those in the noncalcifying area around the GBs. These results indicate that the GBs containing needle-like apatite crystals in morphologic preparations represent sites of chondroitin sulfate degradation. Testicular hyaluronidase-resistant sulfated glycosaminoglycans presumed to be keratan sulfate and partially degraded PGs selectively remain within the GBs as a probable requisite for expansion of the initial calcification in MVs.
J Histochem Cytochem 1983 Sep
PMID:Ultrastructural cytochemistry and immunocytochemistry of proteoglycans associated with epiphyseal cartilage calcification. 613 41


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