47 resultados para Glycoconjugates
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Trypanosoma cruzi trypomastigotes continuously shed into the medium plasma membrane fragments sealed as vesicles enriched in glycoproteins of the gp85 and trans-sialidase (TS) superfamily and alpha-galactosyl-containing glycoconjugates. Injection of a vesicle fraction into BALB/c mice prior to T. cruzi infection led to 40% of deaths on the 16th day post-infection and 100% on day 20th whereas 20% of untreated animals survived for more than 30 clays. The vesicle-treated animals developed severe heart pathology, with intense inflammatory reaction and higher number of amastigote nests. Analysis of the inflammatory infiltrates 15 days after infection showed predominance of TCD4(+) lymphocytes and macrophages, but not of TCD8(+) cells, as well as a decrease of areas labeled with anti-iNOS antibodies as compared to the control. Higher levels of IL-4 and IL-10 mRNAs were found in the hearts and higher IL-10 and lower NO levels in splenocytes of vesicles pretreated animals. Treatment of mice with neutralizing anti-IL-10 or anti-IL-4 antibodies precluded the effects of pre-inoculation of membrane vesicles on infection. These results indicate that T. cruzi shed membrane components increase tissue parasitism and inflammation by stimulation of IL-4 and IL-10 synthesis and thus may play a central role in the pathogenesis of Chagas` disease acute phase. (c) 2008 Elsevier Masson SAS. All rights reserved.
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Lectins have been classified into a structurally diverse group of proteins that bind carbohydrates and glycoconjugates with high specificity. They are extremely useful molecules in the characterization of saccharides, as drug delivery mediators, and even as cellular surface makers. In this study, we present camptosemin, a new lectin from Camptosema ellipticum. It was characterized as an N-acetyl-d-galactosamine-binding homo-tetrameric lectin, with a molecular weight around 26 kDa/monomers. The monomers were stable over a wide range of pH values and exhibited pH-dependent oligomerization. Camptosemin promoted adhesion of breast cancer cells and hemagglutination, and both activities were inhibited by its binding of sugar. The stability and unfolding/folding behavior of this lectin was characterized using fluorescence and far-UV circular dichroism spectroscopies. The results indicate that chemical unfolding of camptosemin proceeds as a two-state monomer-tetramer process. In addition, small-angle X-ray scattering shows that camptosemin behaves as a soluble and stable homo-tetramer molecule in solution.
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The use of glycol methacrylate (GMA) avoids some technical artifacts, which are usually observed in paraffin-embedded sections, providing good morphological resolution. on the other hand, weak staining have been mentioned during the use of different methods in plastic sections. In the present study, changes in the histological staining procedures have been assayed during the use of staining and histochemical methods in different GMA-embedded tissues.Samples of tongue, submandibular and sublingual glands, cartilage, portions of respiratory tract and nervous ganglion were fixed in 4% formaldehyde and embedded in glycol methacrylate. The sections of tongue and nervous ganglion were stained by H&E. Picrosirius, Toluidine Blue and Sudan Black B methods were applied, respectively, for identification of collagen fibers in submandibular gland, sulfated glycosaminoglycans in cartilage (metachromasia) and myelin lipids in nervous ganglion. Periodic Acid-Schiff (PAS) method was used for detection of glycoconjugates in submandibular gland and cartilage while AB/PAS combined methods were applied for detection of mucins in the respiratory tract. In addition, a combination of Alcian Blue (AB) and Picrosirius methods was also assayed in the sublingual gland sections.The GMA-embedded tissue sections showed an optimal morphological integrity and were favorable to the staining methods employed in the present study. In the sections of tongue and nervous ganglion, a good contrast of basophilic and acidophilic structures was obtained by H&E. An intense eosinophilia was observed either in the striated muscle fibers or in the myelin sheaths in which the lipids were preserved and revealed by Sudan Black B. In the cartilage matrix, a strong metachromasia was revealed by Toluidine Blue in the negatively-charged glycosaminoglycans. In the chondrocytes, glycogen granules were intensely positive to PAS method. Extracellular glycoproteins were also PAS positive in the basal membrane and in the region occupied by the lamina externa and reticular fibers surrounding each smooth muscle cells of the blood vessels. In the epithelial cells of the respiratory tract, acid and neutral mucins were histochemically detected by AB and PAS methods, respectively. Moreover, granules containing acid and neutral mucins were revealed in purple by AB and PAS concomitantly. In the sublingual gland sections, a distinct affinity of acid mucins by AB (in turquoise-blue) and collagen fibers by Picrosirius (in red) was obtained when these methods were combined. Although some routine dyes used in paraffin sections have showed a weak stain in historesin sections, our results showed that different dyes could be applied in GMA sections if modified staining procedures were assayed. Therefore, appropriate staining contrast and, thus, detection of one or different substances in a same section can be acquired in association to the good morphological resolution provided by GMA. (C) 2003 Elsevier Ltd. All rights reserved.
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The testicular stroma of the vampire bat including the testicular capsula and the lamina propria of the seminiferous tubuli, was strongly PAS-positive. This observation was a possible indication of great amounts of structural glycogen and other glycoconjugates at the level of smooth muscle cells; elongated contractile cells and/or collagen frameworks of the tunica albuginea and tubular lamina propria. In the last the basement membranes of the seminiferous tubules were particularly strongly PAS positive, as an indication of their neutral mucosubstances structural composition, previously described (Malmi et al., 1987). The epithelium lining from the cavitary and surface rete testis complex showed low reactivities to mucosubstances; total proteins and lipids and oxidative enzymes studied. Although the apical granulation at the rete testis epithelium showed an intense PAS reactivity with hypothesis of glycoprotein secretion, through the rete. The PAS, Sudan Black B, NADH, MDH and LDH reactions of the testicular interstitium seem correlate to steroid metabolism (biosynthesis and secretion), at the Leydig cells level. The seminiferous epithelium generally had low reactions to all the histochemical studies realized. Particularly in the adbasal compartment the histochemical localizations of NADH diaphorase and LDH were possible related to glycolytic activities and general carbohydrates metabolism, both enzymes, and hydrogen transport, the NADH. The strong PAS, diastase and PAS, and alcian blue pH 2.5 and PAS reactions observed in the adluminal seminiferous epithelium compartment were directly related to the spermatids acrosomal glycoconjugates structuration. Also the SDH localization at this level seems to be related to the mitochondrial activities at the middle piece level in the late spermatids.
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The phagocytic process in cells depends on lysosomal enzymes, high-energy metabolism and cellular recognition. In this paper, we investigated the presence of energy and recognition factors in thrombocytes of turtle Phrynopys hilarii (a freshwater South American species). Turtle thrombocytes (P. hilarii) present glycogen - possibly β particles - dispersed in their cytoplasm and glycoproteins in the cell surface, as well as a large number of enzymes involved in the endocytic process (Pellizzon, 1996). The activity of these enzymes depends on high-energy metabolism and on cellular recognition provided by specific glycoconjugates (Alberts et al., 1994). This metabolic characterization is demonstrated by the large amount of glycogen particles observed in the cytoplasm by Thiéry's method. Glycogen labeling was also observed when concanavalin A-peroxidase was used as a marker for thrombocytes and for endocyted charcoal particles. Our results show that these cells have phagocytic ability, suggesting that their function in blood circulation is not limited to aggregation but may also involve a great potential for phagocytosis.
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Spermatogenesis and steroidogenesis undergo seasonal variations during the reproductive cycle in amphibians. Testicular morphological and morphometric seasonal variations as well as interstitial lipidic inclusions and intralobular glycoconjugates were evaluated during seasonal cycle of Rana catesbeiana. Testes of frogs collected during the annual seasons were weighed for calculation of GSI (Gonadosomatic index). Seminiferous lobule diameters (DSL) and volume densities of seminiferous lobules (VvSL), excretory ducts (VvED), and interstitial tissue (VvIT) were analyzed. Semithin sections were submitted to Periodic Acid-Schiff (PAS) and Alcian Blue (AB) methods for detection of glycoconjugates, while lipidic inclusions were detected by Sudan Black B. GSI showed no significant variations during the year. Since VvED and VvIT increased significantly during summer and were inversely proportional to VvSL, a compensatory effect between the testicular compartments may be related to the maintenance of GSI. During autumn/winter, larger lobular diameters were observed in comparison to spring/summer when spermiogenesis and spermiation were commonly observed. The increased VvIT and the numerous lipidic inclusions in the interstitial cells during summer suggest a relationship between spermiogenesis and steroidogenesis. Besides the structural stability variations occurring in the IT and SL, a possible paracrine interaction between ED and IT should be also involved in the IT development during summer. The presence of PAS and AB-positive globular structures were observed in the seminiferous lobules and excretory ducts. These structures containing acid glycoconjugates appear to be Sertoli cell apical portions, which are accumulated in the lumen of the seminiferous lobules mainly during spermiation. © 2004 Wiley-Liss, Inc.
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Studies of sub-lethal effects of pesticide residues on stingless bees are scarce and morphological analysis of organs would add information to toxicological analysis in order to clarify the continuous exposure of Scaptotrigona postica to insecticides. The aim of this study was to evaluate the morphology and histochemistry of the Malpighian tubules (excretory organ) of S. postica exposed to fipronil or boric acid to detect cellular responses that indicate toxicity or adaptative mechanisms to stress induced by exposure of worker bees to low doses of these chemical compounds. Newly emerged bees were submitted to toxicological bioassays and morphological analyses by optical microscopy and Transmission Electron Microscopy, as well as histochemical methods, were performed to detect proteins and glycoconjugates. Additionally, immunohistochemical detection of DNA fragmentation and HSP70 (70-kDa Heat shock protein) were performed to detect cell death and stress response, respectively. Statistical analysis, for the bioassays conducted with ingestion of contaminated diet with boric acid at 0.75% (w/w) or with fipronil at 0.1μg/kg of food, showed that the survival of bees that ingested the contaminated diets were significantly different to the survival rate presented by the control group (P<0.0001). Although some characteristics indicative of initiation of cell death were observed, the cells remained metabolically active in the processes of excretion and inactivation of chemical compounds. The data from this study reinforce the importance of research on sublethal effects of low doses of pesticides on bees in an attempt to assess a possible realistic dose and evaluate the risk assessment of stingless bee S. postica foraging in the vicinity of cultivated fields and/or in green urban areas. © 2013 Elsevier Ltd.
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This study provides histochemical data of the hepatopancreatic cells of adult female pink-shrimp (Farfantepenaeus brasiliensis) at two different developmental stages (those with developed gonads and those with exhausted gonads). The F. brasiliensis females were collected in seawater off the Guarapari coast, Espirito Santo, Brazil. Five cell types were identified in this digestive gland: B (vesicular), E (embryonic), F (fibrillar), M (basal) and R (resorptive). The digestive gland was stained with the following techniques: PAS/Alcian blue (for polysaccharides), bromophenol blue (for protein), von Kossa (for bound calcium) and Baker (for lipids). Acid glycoconjugates were found inside vacuoles in the R cells, while neutral polysaccharides were present in the B cells and near to the microvilli. In females with exhausted gonads polysaccharides were also seen in the intertubular spaces and inside the lumina of the tubules. The F and M cells were the most marked by the presence of large amounts of proteins observed in R cells and also inside the vacuoles of B cells. The bound calcium was mainly found in the F and M cells. The F cells showed strong positive staining for lipid while the R cell only stained weakly. The E cells did not react to any of the applied staining techniques. The similarities in the histochemical composition of these hepatopancreatic cells in females with developed gonads, compared to exhausted ones, is justified by the fact that transfer of these elements to the oocytes occurs, in significant quantity, only during the initial stages of gonadal development in F. brasiliensis. Also, they may be more related to the molt stage, as in the case of calcium salts. © 2013 Elsevier GmbH. All rights reserved.
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
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A leishmaniose tegumentar americana (LTA) constitui uma doença infecciosa causada por protozoários do gênero Leishmania com elevada incidência na região Amazônica. Uma variedade de espécies de leishmania é responsável por esta patologia. Desta forma, dependendo da espécie e da resposta imunológica do hospedeiro vertebrado, a doença pode apresentar diferentes formas clínicas, como a leishmaniose cutânea localizada (LCL) e a leishmaniose mucocutânea (LMC). A principal espécie responsável pela LTA é a Leishmania (Viannia) braziliensis. Contudo, devido à existência de uma multiplicidade de cepas desta espécie e ao reduzido número de estudos relacionados, torna-se importante o conhecimento dos aspectos metabólicos básicos do protozoário, como o metabolismo lipídico, na tentativa de caracterizar vias ou componentes fundamentais para seu desenvolvimento e infectividade. Desta forma, este trabalho teve como objetivo analisar distribuição de corpos lipídicos (CLs) e o perfil lipídico de duas cepas de L. (V.) braziliensis, isolada de diferentes casos clínicos, em diferentes períodos da fase estacionária do crescimento celular. As formas promastigotas das cepas M17593 (LCL) e M17323 (LMC) de L. (V.) braziliensis foram utilizadas na fase estacionária inicial (EST-I) e estacionária tardia (EST-T) de crescimento. Inicialmente, foi realizada análise ultraestrutural das formas promastigotas por microscopia eletrônica de transmissão (MET) e foram observadas estruturas sugestivas de CLs distribuídos no citoplasma do parasito, confirmados pela técnica citoquímica ósmio-imidazol, organelas necessárias para o metabolismo energético do parasito. Para quantificar a distribuição de CLs entre os dias de cultivo e entre as cepas, foi realizada análise por citometria de fluxo com Bodipy® 493/503. Os resultados indicaram que a cepa responsável pela LMC apresentou maior quantidade de CLs durante a fase estacionária tardia. Na cepa LCL não foi observado diferença significativa entre as fases estudadas. Assim, pode ser sugerido que a exacerbada resposta inflamatória que ocorre em pacientes com LMC, esteja relacionada com o acúmulo de CLs no parasito, fonte de energia e eicosanoides, como prostaglandinas. Outra hipótese é a possível correlação de CLs com a baixa exposição do fosfolipídio fosfatidilserina para a superfície externa da membrana, importante para a infectividade do parasito. Para análise dos lipídios totais, os parasitos foram submetidos à extração lipídica, seguido da técnica de HPTLC, onde foram encontrados predominantemente fosfolipídios, esterol esterificado, esteróis, triglicerídeos e ácidos graxos compondo o parasito, com variações entre as cepas e entre as fases estudadas. A cepa LCL na fase estacionária tardia possui maior quantidade de lipídios totais, que pode ser justificado por já ser conhecida como a cepa mais infectiva e possivelmente apresentar maior quantidade de glicoconjugados associados com subdomínios lipídicos importantes para o reconhecimento de fagócitos. É importante ressaltar que a maior infectividade da cepa LCL quando comparada à cepa LMC, resulta em um menor processo inflamatório. Estes resultados indicam que há uma variação no perfil lipídico e na distribuição de CLs entre as diferentes cepas de L. (V.) braziliensis, que pode estar relacionado com a infectividade do parasito e com a manifestação clinica da doença.
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Pós-graduação em Medicina Veterinária - FCAV
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A parede celular micobacteriana é uma característica marcante do gênero Mycobacterium, apresentando lipídios e glicoconjugados bioativos, como fosfatidilinositol manosídeos (PIMs), lipomanana (LM) e lipoarabinomanana (LAM). A infecção crônica no interior de macrófagos pulmonares é relacionada com o acúmulo de colesterol na célula hospedeira, conferindo uma fonte alternativa de energia e carbono para o bacilo manter suas funções fisiológicas. Com base na atividade imunomoduladora desses glicoconjugados e na adaptação em outro ambiente no interior da célula hospedeira infectada, propomos investigar a possível modulação da biossíntese de LM/LAM em Mycobacterium smegmatis (saprofítico), após o cultivo em meio mínimo (MM) suplementado com glicerol e/ou colesterol. Como resultados, obtivemos que o bacilo, mesmo sendo saprofítico, foi capaz de acumular colesterol e influenciar na fisiologia bacteriana por apresentar um crescimento lento com densidade bacteriana comprometida. Além disso, o colesterol diminuiu o acúmulo de PIMs e promoveu mudanças morfológicas e de agregação bacteriana, mesmo mantendo a parede celular com sua característica físico-química específica (resistência a descoloração por álcool e ácido). A mudança mais marcante induzida pelo consumo do colesterol foi na biossíntese de LAM, que apresentou migração eletroforética diferenciada, compatível às massas moleculares maiores, assemelhando-se a de bacilos não saprofíticos (de 25 – 30 KDa para 30 – 50 KDa). Estes resultados mostram que o colesterol, quando utilizado como principal alternativa de fonte de energia e carbono, pode induzir mudanças fisiológicas em micobactérias, principalmente na biossíntese de LAM, uma das principais moléculas imunoreguladoras presente na parede celular. Estes dados sugerem que micobactérias podem sofrer mudanças semelhantes no interior de granulomas, e que estas mudanças podem ajudar na evolução da tuberculose para a forma crônica multibacilar, marcada por um aspecto imunodeficiente contra o bacilo.
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Coordenação de Pessoal de Nível Superior (CAPES)
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)