Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 10 de 10
Filter
1.
An. bras. dermatol ; 91(5): 595-600, Sept.-Oct. 2016. graf
Article in English | LILACS | ID: biblio-827746

ABSTRACT

Abstract: Background: Heparanase is an enzyme that cleaves heparan sulfate chains. Oligosaccharides generated by heparanase induce tumor progression. Basal cell carcinoma and squamous cell carcinoma comprise types of nonmelanoma skin cancer. Objectives: Evaluate the glycosaminoglycans profile and expression of heparanase in two human cell lines established in culture, immortalized skin keratinocyte (HaCaT) and squamous cell carcinoma (A431) and also investigate the expression of heparanase in basal cell carcinoma, squamous cell carcinoma and eyelid skin of individuals not affected by the disease (control). Methods: Glycosaminoglycans were quantified by electrophoresis and indirect ELISA method. The heparanase expression was analyzed by quantitative RT-PCR (qRTPCR). Results: The A431 strain showed significant increase in the sulfated glycosaminoglycans, increased heparanase expression and decreased hyaluronic acid, comparing to the HaCaT lineage. The mRNA expression of heparanase was significantly higher in Basal cell carcinoma and squamous cell carcinoma compared with control skin samples. It was also observed increased heparanase expression in squamous cell carcinoma compared to the Basal cell carcinoma. Conclusion: The glycosaminoglycans profile, as well as heparanase expression are different between HaCaT and A431 cell lines. The increased expression of heparanase in Basal cell carcinoma and squamous cell carcinoma suggests that this enzyme could be a marker for the diagnosis of such types of non-melanoma cancers, and may be useful as a target molecule for future alternative treatment.


Subject(s)
Humans , Skin Neoplasms/enzymology , Carcinoma, Basal Cell/enzymology , Carcinoma, Squamous Cell/enzymology , Glucuronidase/metabolism , Glycosaminoglycans/metabolism , RNA, Messenger/metabolism , Keratinocytes/metabolism , Eyelids/enzymology , Real-Time Polymerase Chain Reaction/methods , Glucuronidase/genetics , Glycosaminoglycans/analysis , Hyaluronic Acid/analysis , Hyaluronic Acid/metabolism
2.
Braz. j. microbiol ; 44(4): 1097-1104, Oct.-Dec. 2013. graf, tab
Article in English | LILACS | ID: lil-705288

ABSTRACT

In this work, natural cashew apple juice was used as cultivation medium as an alternative to substitute brain heart infusion medium. The effect of aeration and juice supplementation with yeast extract on the production of hyaluronic acid in batch fermentation was also investigated. Similar levels of cell mass were obtained in inoculum using cashew apple juice supplemented with yeast extract or the conventional brain heart infusion medium. Fermentation in Erlenmeyer flasks produced low biomass and hyaluronic acid concentrations. The hyaluronic acid concentration and viscosity increased from 0.15 g/L and 3.87 cP (no aeration or medium supplementation) to 1.76 g/L and 107 cP, when aeration (2 vvm) and 60 g/L of yeast extract were used. The results suggest the production of low-molecular weight hyaluronic acid oligomers instead of the high molecular weight polymer.


Subject(s)
Anacardium/chemistry , Culture Media/chemistry , Hyaluronic Acid/metabolism , Saccharomyces cerevisiae/growth & development , Saccharomyces cerevisiae/metabolism , Biomass , Fermentation
3.
Braz. j. otorhinolaryngol. (Impr.) ; 78(3): 14-18, maio-jun. 2012. tab
Article in Portuguese | LILACS | ID: lil-638575

ABSTRACT

A vibração das pregas vocais é um importante fator envolvido na produção vocal e o envelhecimento pode alterar a quantidade de ácido hialurônico da prega vocal levando a disfonia. OBJETIVO: Este estudo compara a concentração de ácido hialurônico nas pregas vocais de ratas fêmeas idosas e jovens. Desenho do estudo: estudo experimental. MATERIAL E MÉTODO: Foram utilizadas pregas vocais de 13 ratas fêmeas divididas em dois grupos: cinco ratas idosas e oito ratas jovens. A concentração tecidual do ácido hialurônico foi determinada por meio de método fluorimétrico utilizando a proteína de ligação ao ácido hialurônico imobilizada em placas de enzyme-linked immunosorbent assay (ELISA) e também conjugada à biotina. Estreptavidina marcada com európio foi adicionada e, depois de európio ter sido liberado com o uso de solução de enhancement; a fluorescência final foi medida em um fluorímetro. RESULTADOS: Foram encontradas as seguintes concentrações de ácido hialurônico nas pregas vocais de acordo com os grupos: 581,7 ng/mg em ratas idosas e 1275,6 ng/mg em ratas jovens. A análise estatística mostrou diferença entre os grupos. CONCLUSÃO: A prega vocal de ratas idosas tem uma menor concentração de ácido hialurônico do que a concentração da prega vocal de ratas jovens.


The vibration of the vocal fold lamina propria is an important factor involved in vocal production and aging may change the amount of hyaluronic acid in the vocal fold leading to dysphonia. AIMS: This study compares the concentration of hyaluronic acid in vocal folds of aged and young female rats. Study design: experimental. MATERIALS AND METHODS: We used the vocal cords of 13 female rats divided into two groups: five aged rats and eight young ones. The tissue concentration of hyaluronic acid was determined using the fluorimetric method with the hyaluronic acid binding-protein coated on plates of enzyme-linked immunosorbent assay (ELISA), conjugated with biotin. Europium-labeled streptavidin was added and, after europium release with the use of enhancement solution, the final fluorescence was measured in a fluorometer. RESULTS: We found the following concentrations of hyaluronic acid in vocal fold according to the group: 581.7 ng/mg in old female rats and 1275.6 ng/mg in young female rats. Statistical analysis showed differences between groups. CONCLUSIONS: The vocal folds of old female rats have a lower concentration of hyaluronic acid when compared to such concentration on the vocal folds of young female rats.


Subject(s)
Animals , Female , Rats , Aging/metabolism , Hyaluronic Acid/analysis , Vocal Cords/chemistry , Age Factors , Enzyme-Linked Immunosorbent Assay , Hyaluronic Acid/metabolism , Rats, Wistar
4.
Braz. oral res ; 26(2): 139-144, Mar.-Apr. 2012. ilus, tab
Article in English | LILACS | ID: lil-622910

ABSTRACT

Little is known about the histogenesis of the odontogenic myxoma (OM). Dental pulp stem cells could be candidate precursors of OM because both OM and the dental pulp share the same embryological origin: the dental papilla. For the purpose of comparing OM and stem cells, this study analyzed the expression of two proteins related to OM invasiveness (MMP-2 and hyaluronic acid) in human immature dental pulp stem cells (hIDPSCs). Three lineages of hIDPSCs from deciduous and permanent teeth were used in this study. Immunofluorescence revealed positive reactions for MMP-2 and hyaluronic acid (HA) in all hIDPSCs. MMP-2 appeared as dots throughout the cytoplasm, whereas HA appeared either as diffuse and irregular dots or as short fibrils throughout the cytoplasm and outside the cell bodies. The gene expression profile of each cell lineage was evaluated using RT-PCR analysis, and HA was expressed more intensively than MMP-2. HA expression was similar among the three hIDPSCs lineages, whereas MMP-2 expression was higher in DL-1 than in the other cell lines. The expression of proteins related to OM invasiveness in hIDPSCs could indicate that OM originates from dental pulp stem cells.


Subject(s)
Adolescent , Child , Child, Preschool , Humans , Dental Pulp/metabolism , Hyaluronic Acid/metabolism , /metabolism , Myxoma/pathology , Odontogenic Tumors/pathology , Stem Cells/metabolism , Cells, Cultured , Dental Pulp/cytology , Extracellular Matrix , Fluorescent Antibody Technique , Gene Expression , Hyaluronic Acid/genetics , /genetics , Myxoma/genetics , Neoplasm Invasiveness/pathology , Odontogenic Tumors/genetics , Reverse Transcriptase Polymerase Chain Reaction
5.
Rev. bras. otorrinolaringol ; 74(2): 201-206, mar.-abr. 2008. ilus, tab
Article in English, Portuguese | LILACS | ID: lil-484825

ABSTRACT

O receptor do ácido Hialurônico é uma glicoproteína da membrana plasmática, sendo o principal o CD44, e está expresso em vários tipos de células onde possui a função de adesão celular. OBJETIVO: Estudar a possibilidade de empregar o método imunohistoquímico para identificar a distribuição dos receptores de ácido hialurônico ao longo da prega vocal humana. MATERIAL E MÉTODOS: Foram ressecadas as pregas vocais normais de um indivíduo de 23 anos, sexo masculino, cor negra. As lâminas foram analisadas por meio de estudo histomorfométrico, comparando-se a intensidade das cores nas camadas superficial, média e profunda da lâmina própria. Nas lâminas silanizadas foi utilizado método imunohistoquímico, sendo avaliadas através de microscopia óptica com aumento 40 vezes, obtendo coloração marrom onde houve a reação com receptor para ácido hialurônico. RESULTADOS: Os achados imunohistoquímicos mostraram presença de receptores para ácido hialurônico no epitélio de cobertura da prega vocal tendo maior concentração na região central da prega vocal. CONCLUSÃO: A técnica de imunohistoquímica, utilizada para avaliar a distribuição dos receptores para ácido hialurônico na pregas vocais humanas, mostrou sua disposição em epitélio da prega vocal e predomínio no terço médio, em relação às demais regiões na prega vocal estudada.


Hyaluronic acid receptor is a glycoprotein of the plasmatic membrane, and the CD44 is its representative, expressed in many cell types where it has the task of cell adhesion. AIM: the goal of the present experimental study is to investigate the possibility of using immunohistochemistry to identify the distribution of hyaluronic acid along the vocal fold. MATERIALS AND METHODS: We resected the normal vocal folds from a normal 23 year-old male black individual. The slides were analyzed by means of a histomorphometric study, comparing the color intensity in the superficial, middle and deep layers of the lamina propria. In the silanized slides we used immunohistochemistry, and evaluated the slides under light microscopy with 40x magnification, and the color changed to brown when there was a reaction with the receptor for hyaluronic acid. RESULTS: Immunohistochemical findings showed the presence of hyaluronic acid receptors in the epithelium covering the vocal fold, being more concentrated in the central region of the vocal fold. CONCLUSION: immunohistochemistry, used to assess the distribution of hyaluronic acid receptors in the central portion of the vocal fold, proved it to be present in the vocal fold epithelium and it prevailed in its middle third.


Subject(s)
Adult , Humans , Male , /analysis , Hyaluronic Acid/metabolism , Vocal Cords/chemistry , Black People , Alcian Blue , Cadaver , Coloring Agents , White People , Immunohistochemistry , Vocal Cords/anatomy & histology , Vocal Cords/cytology
6.
Indian J Exp Biol ; 2005 Nov; 43(11): 1023-31
Article in English | IMSEAR | ID: sea-58694

ABSTRACT

With increasing medical utilization of assisted reproductive technology (ART), scientists and clinicians have been able to study extensively multiple cell functions operating synchronously and flawlessly during the events preceding, before and after fertilization. Critical evaluation of the functional status of spermatozoa for in vitro techniques such as sperm-mucus interaction, acrosome reaction status, sperm-zona pellucida binding and penetration tests, hyaluronic acid binding assay, and computer assisted semen analysis etc. can direct a male partner of an infertile couple to more aggressive forms of treatments. In vitro selection of functionally competent sperm cells is a pre-requisite for successful outcome in in vitro fertilization or in intracytoplasmic sperm injection (ICSI). Direct injections of acrosome-intact spermatozoa into oocyte during ICSI bypassing the normal events of sperm oocyte interaction and fusion events have raised concerns with regard to fertilization abnormalities and genetic issues. The present communication briefly reviews the sperm function tests with emphasis on its correlation with fertility outcome, and the currently employed sperm selection and manipulation procedures which may have implications in assisted conception programs.


Subject(s)
Acrosome Reaction , Animals , Cell Membrane/metabolism , Cell Nucleus/metabolism , Cell Survival , Embryo, Mammalian/cytology , Female , Fertilization , Germ Cells , Humans , Hyaluronic Acid/metabolism , Male , Protein Binding , Reproductive Techniques, Assisted , Sperm Injections, Intracytoplasmic/methods , Sperm-Ovum Interactions , Spermatozoa/metabolism , Zona Pellucida/metabolism
7.
Indian J Pathol Microbiol ; 2005 Jan; 48(1): 1-3
Article in English | IMSEAR | ID: sea-74169

ABSTRACT

Gelatinous marrow transformation (GMT) is an uncommon and poorly recognized condition characterized by deposition of seromucinous gelatinous material in the bone marrow stroma. Forty-three cases of GMT were studied in a period of 4 years. There was male preponderance. Fourteen cases were in pediatric age group (less than 12 years). Majority of patients had a preceding history of anorexia, malnutrition and chronic debility. All the patients had anemia. Bone marrow biopsy revealed focal or diffuse GMT. Bone marrow aspirate showed metachromatic dense mucoid material with a few entrapped hematopoietic cells on Giemsa staining. The gelatinous material stained with alcian blue at pH 2.5.


Subject(s)
Adolescent , Adult , Aged , Anorexia/complications , Biopsy, Needle , Bone Marrow/pathology , Bone Marrow Diseases/pathology , Child , Child, Preschool , Chronic Disease , Female , Gelatin , Humans , Hyaluronic Acid/metabolism , India , Infant , Male , Malnutrition/complications , Middle Aged , Staining and Labeling
8.
Saudi Medical Journal. 2003; 24 (7): 715-9
in English | IMEMR | ID: emr-64650

ABSTRACT

Hairy cell leukemia is a chronic B cell leukemia with a number of distinctive features including the unusual tissue distribution of the leukemic cells, hairy cells, and the bone marrow fibrosis. We have been working, for a number of years, on the potential mechanisms behind hairy-cell localization in tissues. In this review, it is summarized how our work has shed very important information regarding these mechanisms and led, eventually, to the full elucidation of the process of the bone marrow fibrosis in hairy cell leukemia


Subject(s)
Humans , Leukemia, Hairy Cell/physiopathology , /metabolism , Bone Marrow/pathology , Immunohistochemistry , Hyaluronan Receptors/physiology , Fibrosis , Fibronectins/metabolism , Hyaluronic Acid/metabolism , Integrins/physiology
9.
Yonsei Medical Journal ; : 193-202, 2002.
Article in English | WPRIM | ID: wpr-89646

ABSTRACT

A hyaluronic acid (HA) incorporated porous collagen matrix was fabricated at -70 degree C by lyophilization. The HA incorporated collagen matrix showed increased pore size in comparison with collagen matrix. Biodegradability and mechanical properties of matrices were controllable by varying the ultraviolet (UV) irradiation time for cross-linking collagen molecules. Addition of HA to collagen matrix did not effect ultimate tensile stress after UV irradiation. HA incorporated collagen matrices demonstrated a higher resistance against the collagenase degradation than collagen matrix. In an in vitro investigation of cellular behavior using dermal fibroblasts on the porous matrix, HA incorporated collagen matrix induced increased dermal fibroblast migration and proliferation in comparison with collagen matrix. These results suggest that the HA incorporated collagen porous matrix assumes to enhance dermal fibroblast adaptation and regenerative potential.


Subject(s)
Humans , Collagen/metabolism , Extracellular Matrix/metabolism , Fibroblasts/physiology , Hyaluronic Acid/metabolism , Porosity
10.
Vet. Méx ; 24(2): 113-6, abr.-jun. 1993. tab, ilus
Article in Spanish | LILACS | ID: lil-121215

ABSTRACT

Se aislaron 20 cepas de P. multocida de pulmones de cerdo. Siete cepas lisas pertenecieron al grupo capsular D, mientras que 12 cultivos de la variedad mucoide y uno con colonias lisas se lasificaron como serotipo A por la prueba de hemoaglutinaciòn indirecta (HI). Se usó una prueba de cromatografía en papel para detectar la presencia de ácido hialurónico. El material capsular de todas las cepas usadas en el estudio mostró un patrón de movimiento al mismo nivel que el ácido hialurónico purificado. Los cultivos del serogrupo A mostraron una mancha más clara y grande que los cultivos del serogrupo D. Los resultados sugieren que el material capsular de las cepas del grupo D pueden contener ácido hialurónico como las del serotipo A, o que pueden tener una substancia diferente que migra al mismo nivel.


Subject(s)
Animals , Male , Pasteurella/isolation & purification , Hyaluronic Acid/metabolism , Serotyping/methods , Swine/microbiology , Blood/microbiology
SELECTION OF CITATIONS
SEARCH DETAIL