Tsang Po Ting. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2006. / Includes bibliographical references (leaves 135-152). / Abstracts in English and Chinese. / Acknowledgements --- p.i / Abstract --- p.ii / Abstract 摘要 --- p.iv / List of Figures --- p.vi / List of Tables --- p.viii / List of Abbreviations --- p.ix / Table of Contents --- p.xii / Chapter Chapter 1: --- General Introduction --- p.1 / Chapter 1.1 --- The Role of Glucose in Biological System --- p.1 / Chapter 1.2 --- Glucose Transporter Families --- p.1 / Chapter 1.2.1 --- Na+-Dependent Glucose Transporters --- p.2 / Chapter 1.2.2 --- Facilitative Glucose Transporters --- p.3 / Chapter 1.3 --- Glucose Transporter Type1 --- p.7 / Chapter 1.3.1 --- Primary Structure of the Glutl Protein --- p.7 / Chapter 1.3.2 --- Secondary Structure --- p.8 / Chapter 1.3.3 --- Tertiary Structure --- p.8 / Chapter 1.3.4 --- Kinetics Properties --- p.11 / Chapter 1.3.5 --- Tissue Distribution --- p.12 / Chapter 1.3.6 --- Multifunctional Property --- p.13 / Chapter 1.3.7 --- Characterization of GLUT1 Gene --- p.13 / Chapter 1.3.8 --- Regulation of GLUT1 Expression --- p.14 / Chapter 1.4 --- Glucose Transporter Type 1 and the Brain --- p.16 / Chapter 1.5 --- Glucose Transporter Type 1 Deficiency Syndrome (GIutlDS) --- p.19 / Chapter 1.5.1 --- Backgronnd of GIutlDS --- p.19 / Chapter 1.5.2 --- Clinical Features of GIutlDS --- p.23 / Chapter 1.5.3 --- Genotype-Phenotype Correlations --- p.24 / Chapter 1.5.4 --- Diagnosis --- p.26 / Chapter 1.5.5 --- Manage nent --- p.27 / Chapter 1.5.5.1 --- Ketogenic Diet --- p.27 / Chapter 1.6 --- Hypothesis and Objectives --- p.29 / Chapter Chapter 2: --- Biochemical and Molecular Analysis of GLUT1 in a Suspected GlutlDS Case --- p.31 / Chapter 2.1 --- Materials --- p.32 / Chapter 2.1.1 --- Clinical History of Suspected GlutlDS Patient --- p.32 / Chapter 2.1.2 --- Blood Samples --- p.32 / Chapter 2.1.3 --- Reagents and Buffers for Reverse Transcription --- p.32 / Chapter 2.1.4 --- Reagents and Buffers for TA Cloning --- p.34 / Chapter 2.1.5 --- Reagents for Genomic DNA Extraction --- p.34 / Chapter 2.1.6 --- Reagents and Buffers for Polymerase Chain Reaction (PCR) --- p.34 / Chapter 2.1.7 --- Reagents and Buffers for Agarose Gel Electrophoresis --- p.35 / Chapter 2.1.8 --- Reagents for Zero-trans 3-OMG Influx in Erythrocytes --- p.37 / Chapter 2.1.9 --- Reagents for Zero-trans 3-OMG Efflux from Erythrocytes --- p.38 / Chapter 2.1.10 --- Reagents for Erythrocytes Membrane Extraction and Detection --- p.39 / Chapter 2.2 --- Methods --- p.44 / Chapter 2.2.1 --- GLUT1 Gene Analysis --- p.44 / Chapter 2.2.2 --- Zero-trans 3-OMG Influx into Erythrocytes --- p.51 / Chapter 2.2.3 --- Zero-trans 3-OMG Efflux from Erythrocytes --- p.52 / Chapter 2.2.4 --- Glutl Protein Expression --- p.54 / Chapter 2.2.5 --- Statistics --- p.57 / Chapter 2.3 --- Results --- p.58 / Chapter 2.3.1 --- Molecular Analysis of the GLUT1 Gene of a Suspected GlutlDS Patient --- p.58 / Chapter 2.3.2 --- Functional Analysis of the GlutlDS Patient's Glutl Protein --- p.61 / Chapter 2.3.3 --- Glutl Protein Expression in the GlutlDS Patient --- p.64 / Chapter 2.4 --- Discussion --- p.66 / Chapter Chapter 3: --- Pathogenicity Studies of GLUT1 Mutations --- p.71 / Chapter 3.1 --- Materials --- p.72 / Chapter 3.1.1 --- Construction of Glutl-Encoding Vectors --- p.72 / Chapter 3.1.2 --- Cell Lire --- p.73 / Chapter 3.1.3 --- "Cell Culture Media, Buffers and Other Reagents" --- p.73 / Chapter 3.1.4 --- Cell Culture Wares --- p.75 / Chapter 3.1.5 --- Reagents for Transfection --- p.75 / Chapter 3.1.6 --- Reagents for Protein Determination and Western Blot Analysis --- p.76 / Chapter 3.1.7 --- Consumables for Confocal Microscopy --- p.77 / Chapter 3.1.8 --- Reagents and Buffers for Flow Cytometry --- p.77 / Chapter 3.1.9 --- Reagents for 2-DOG Uptake in CHO-K1 Cells --- p.77 / Chapter 3.2 --- Methods --- p.79 / Chapter 3.2.1 --- Cell Culture Methodology --- p.79 / Chapter 3.2.2 --- Construction of GLUT1 Mutants --- p.80 / Chapter 3.2.3 --- Establishment of Wild Type and Mutant Glutl Expressing Cell Lines --- p.84 / Chapter 3.2.4 --- Protein Expression Study --- p.85 / Chapter 3.2.5 --- 2-DOG Influx Assay in CHO-K1 Cells --- p.87 / Chapter 3.2.6 --- Confocal Microscopy Studies on Glutl Cellular Localization --- p.89 / Chapter 3.2.7 --- Statistics --- p.90 / Chapter 3.3 --- Results --- p.91 / Chapter 3.3.1 --- Molecular Analysis of 1034-1035Insl2 Mutation --- p.91 / Chapter 3.3.2 --- Expression of the Wild Type and Mutant GFP-Glutl Fusion Proteins --- p.92 / Chapter 3.3.3 --- Functional Analysis of the 1034-1035Insl2 Mutant --- p.95 / Chapter 3.4 --- Discussion --- p.97 / Chapter Chapter 4: --- GLUT1 Promoter Study --- p.100 / Chapter 4.1 --- Materials --- p.101 / Chapter 4.1.1 --- Construction of GLUT1 Promoter Vectors --- p.101 / Chapter 4.1.2 --- Cell Lines --- p.102 / Chapter 4.1.3 --- Cell Culture Media and Other Reagents --- p.103 / Chapter 4.1.4 --- Dual Luciferase Reporter Assay System --- p.103 / Chapter 4.2 --- Methods --- p.105 / Chapter 4.2.1 --- Bioinformatics --- p.105 / Chapter 4.2.2 --- Cell Culture --- p.105 / Chapter 4.2.3 --- Construetion of GLUT1 Promoter Vectors --- p.105 / Chapter 4.2.4 --- 5'-Deletion Analysis of GLUT1 Promoter --- p.108 / Chapter 4.2.5 --- Determination of the Activities of GLUT1 Promoter Fragments --- p.110 / Chapter 4.2.6 --- Statistics --- p.113 / Chapter 4.3 --- Results --- p.114 / Chapter 4.3.1 --- Determination of the Promoter Activity of the 5'-deletion Fragments --- p.114 / Chapter 4.3.2 --- Prediction of Transcription Factors in the 5'-deletion Fragments --- p.119 / Chapter 4.4 --- Discussion --- p.121 / Chapter Chapter 5: --- General Conclusion and Future Perspectives --- p.133 / References --- p.135

Zinc is the second most abundant transition metal in biological systems. This cation is required for the catalytic activity of hundreds of enzymes which mediate protein synthesis, DNA replication and cell division. Despite the central importance of zinc in cellular homeostasis, the mechanism of zinc uptake, compartmentalization and efflux is unknown. Recently, a family of proteins, called ZIP, has been shown to control zinc uptake. Mutations in one of the genes coding for these proteins (ZIP4) can lead to potentially life-threatening diseases like Acrodermatitis Enteropathica and high levels of ZIP4 have been detected in patients suffering from pancreatic cancer. Therefore our goal is to investigate the mechanism of ZIP4 transport and regulation. It was previously shown that the intracellular loop between transmembrane III and IV (M3M4) of ZIP4 is ubiquitinated in the presence of high intracellular zinc which lead to protein degradation. Our initial hypothesis was that the large intracellular domain of ZIP4 (M3M4) is a sensor which detects the intracellular concentration of zinc and regulates the surface expression of ZIP4. In order to test this hypothesis we expressed and purified the M3M4 domain to examine the ability of M3M4 to bind zinc. Our results have demonstrated that M3M4 binds zinc with a 2:1 zinc:protein stoichiometry with nanomolar affinity. We have also shown that upon binding of zinc, M3M4 undergoes a large conformational change.

Med väl fungerande interna logistiska flöden kan hela produktionen effektiviseras samtidigt som man kan skapa mer bränsleeffektiva transporter. Ett företag som är intresserade av att både kunna arbeta mer effektivt med sina transporter och spara på bränsle både för miljön och för kostnadernas skull är Vargön Alloys AB i Vargön utanför Vänersborg.Vargön Alloys är en av Europas största tillverkare av olika Ferrolegeringar. Legeringar ger bl.a. stålet hårdhet och förhindrar korrosion. Företagets kunder är Europas ledande tillverkare av specialstål.Ett problem för Vargön Alloys har varit att man inte har någon dokumentation eller kartläggning över hur de interna transporterna sker idag. Syftet med detta examensarbete är därför att kartlägga hur Vargön Alloys interna transporter sker idag samt att ge förslag till effektivisering, både vad gäller arbetsmetoder och lagerplanering, som leder till minskad bränsleförbrukning samt mindre trafik på fabriksområdet.En kvalitativ undersökningsmetod har använts där observationer följts av intervjuer med personer med olika arbetsområden på företaget. Intervjuobjekten har till största del fått vara anonyma och intervjuerna har skett individuellt med öppna frågor. Användbara teorier studerades i lämpliga läroböcker.Observationer och intervjuer har resulterat i en värdefödeskarta över informationsflödena samt en spagettikarta över transportflödena. Efter analys av dessa har ett antal förbättringsförlag framkommit. Genom att använda nya moderna tekniker som hjälpmedel i arbetet skulle Vargön Alloys definitivt kunna effektivisera sina interna transporter till att bli mer bränsleeffektiva. Med hjälp av ett verktyg som t. ex. GPS timber skulle förtaget få ett system som innehåller både planeringssystem, lagerstyrning och ett GPS-system i fordonen.

Detta examensarbete har utförts under höstterminen 2008 på Högskolan i Borås på uppdrag av Flügger AB i Bollebygd. År 1994 köpte Flügger A/S upp HP Färg & Kemi och kedjan Flügger AB startades i Sverige. Idag har Flügger i Bollebygd 150 anställda, vilket gör dem till en av Bollebygds största arbetsgivare. Dagens fabrik i Bollebygd är uppdelad i fyra producerande enheter; Alkyd-, Latex-, Kemi- och Spackelfabrik. Fabrikerna rymmer produktion av vattenbaserad- och terpentinbaserad färg, träskydd, spackelprodukter, rengöringsmedel för industri och biltvättsanläggningar, samt målningsrelaterade rengöringsmedel. I Bollebygd finns även ett råvaru- och emballagelager som ansvarar för materialtillförsel till de fyra produktionsenheterna. Syftet med detta arbete är att hitta förbättringar och effektiviseringsförslag för nuvarande interna transporter från råvaru- och emballagelager. Målsättningen är även att hitta lösningar för mellanlagringsplatser, samt förslag till utformning av råvaru- och emballagelager. En ytterligare uppgift är att hitta ett tillvägagångssätt som förbättrar beställningsrutiner och returhantering. Behovssvängningar skall jämnas ut genom att sprida ut de interna beställningarna till råvaru- och emballagelagret. I och med att företaget är certifierat enligt ISO 14 001 skall ovanstående punkter utföras med hänsynstagande till miljön. Genom intervjuer med de anställda på Flügger har information erhållits om de problem som finns inom internlogistik och lagerhantering. Intervjuer har även gjorts för att ta vara på de eventuella förbättringsförslag de anställda besitter. För att få en sådan korrekt helhetsbild som möjligt har både lagerpersonal och fabrikspersonal intervjuats. Observationer har gjorts på lagret såväl som på produktionsenheterna. På lagret har även tidtagning av lageraktiviteter utförts. En klar bild av Flüggers interna logistik och lageraktiviteter har erhållits under arbetets gång. Utifrån den bilden dras slutsatsen att aktiviteterna kan effektiviseras och att Flügger med relativt små medel kan förändra bilden till det bättre. Ett antal förbättringsförslag har framtagits inom de olika problemområdena. Dessa innehåller bland annat en presentation av lagerutformning, beställningsrutin samt effektivisering av lageraktiviteter.

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Xanthomonas citri (X. citri), causador do cancro cítrico, afeta muitas áreas de cultivo de citros com impacto comercial. Transportadores ABC foram relatados como essenciais para a patogênese de X. citri. O gene nrtT codifica a proteína periplasmática responsável pelo suposto transporte de nitrato/nitrito/taurina. Neste trabalho, mostramos que a deleção de nrtT não afeta o crescimento de X. citri, porém reduz e atrasa os sintomas do cancro durante a infecção em folhas de citros. Observamos redução na produção de goma xantana e capacidade de aderência na linhagem mutante. A proteína NrtT foi expressa monomérica e monodispersa. Foram observadas alterações na estrutura secundária e aumento da estabilidade térmica de NrtT na presença de MOPS, indicando ser este um possível ligante de NrtT. A proteína PotF descrita como ligadora de putrescina não sofre alteração significativa na estabilidade térmica na presença de putrescina, entretanto, dados de SAXS mostram alterações na estrutura possivelmente decorrentes da ligação com putrescina. / Xanthomonas citri (X. citri), which causes citrus canker, affects many citrus growing areas with commercial impact. ABC transporters have been reported as essential for the pathogenesis of X. citri. The nrtT gene encodes the periplasmic protein responsible for the alleged transport of nitrate/nitrite/taurine. In this work, we show that nrtT deletion does not affect the growth of X. citri, but delays and reduces the symptoms of cancer during infection of citrus leaves. We observed a reduction in the production of xanthan gum and adhesion capacity in the mutant strain. The NrtT protein was expressed monomeric and monodisperse. There were changes in the secondary structure and increased thermal stability NrtT in the presence of MOPS, indicating that this was a possible binder NrtT. The PotF protein described as putrescine-binding is not significantly altered thermal stability in the presence of putrescine, however, SAXS data shows changes in the structure possibly resulting from connection with putrescine.

Depuis le début des années 1990, différentes stratégies de phytoremédiation ont été proposées pour réhabiliter les zones polluées par des éléments traces métalliques (ETM). Parmi ces stratégies, la phytoextraction consiste en l’absorption et l’accumulation par les plantes des ETM présents dans les sols. Afin de mettre en place cette stratégie, il a été proposé d’utiliser le peuplier en raison de sa croissance rapide, de son importante biomasse et de ses débouchés énergétiques. Cependant une proportion considérable des métaux absorbés par cet arbre est accumulée dans les feuilles alors que celles-ci chutent à l’automne. Ainsi, l’efficacité de phytoextraction du peuplier peut se trouver limitée si aucun mécanisme de remobilisation des ETM n’est mis en place au cours de la sénescence automnale. Dans ce contexte, une partie des travaux de cette thèse a été réalisée sur la parcelle expérimentale de Pierrelaye polluée suite à l’épandage d’eaux usées de la ville de Paris. Nous avons recherché parmi les 14 génotypes de peuplier présents sur le site, ceux qui sont les plus efficaces pour remobiliser les métaux des feuilles vers les parties pérennes. Des mesures de contenu en métaux, d’expression de gènes et des analyses corrélatives ont ouvert de nouvelles pistes concernant la gestion des métaux foliaires. Parce que la vacuole constitue le principal lieu de stockage des métaux de la cellule, les protéines d’efflux vacuolaire NRAMP (Natural Resistance-Associated Macrophage Protein) précédemment identifiées chez Arabidopsis thaliana, représentent de bons candidats pour stimuler la remobilisation des métaux foliaires. La caractérisation de leurs homologues chez le peuplier a donc été entreprise par expression chez la levure et chez A. thaliana. Afin de contrôler indépendamment le transport des métaux essentiels et non-essentiels chez les NRAMP, une étude visant à identifier les déterminants structuraux impliqués dans leur sélectivité a été réalisée. La caractérisation des mutants NRAMP affectés dans leur sélectivité par expression chez A. thaliana a mis en lumière leur impact sur l’accumulation et la tolérance aux métaux. Dans le but d’étudier l’implication de mécanismes plus généraux de recyclage des nutriments dans la remobilisation des métaux au cours de la sénescence foliaire, le rôle de l’autophagie a été testé chez A. thaliana. L’étude de plantes déficientes pour l’autophagie a montré l’implication de ce mécanisme dans l’efficacité d’utilisation des métaux et probablement dans leur remobilisation au cours de la sénescence. En combinant des études en champ sur le peuplier et de génétique moléculaire chez Arabidopsis, ce travail permet de proposer différentes pistes pour diminuer spécifiquement l’accumulation des ETM dans les feuilles de peuplier. / Since the early 1990s, various strategies have been proposed to rehabilitate trace element (TE) polluted areas by phytoremediation. Among these strategies, phytoextraction consists in TE uptake from soil and accumulation by plants. To implement this strategy, it has been proposed to use poplar due to its fast growth, its large biomass and its use in energy production. However, a substantial proportion of absorbed metals is accumulated in poplar leaves which fall in autumn. Thus, poplar phytoextraction efficiency may be limited if TE are not re-mobilized during autumn senescence. In this context, part of this thesis work has been carried out on the experimental field of Pierrelaye which was polluted by the spreading of sewage water from Paris. Among the 14 poplar genotypes growing on the field, we tried to identify those that efficiently remobilize leaf metals to perennial organs. Metal content, gene expression and correlative analyses have been undertaken, providing new insight in the management of metals in leaves. Because the vacuole is the main metal storage compartment in the cell, NRAMP (Natural Resistance-Associated Macrophage Protein) vacuolar efflux proteins previously identified in Arabidopsis thaliana are good candidates to enhance leaf metal remobilization. Characterization of their homologues in poplar was therefore undertaken by expression in yeast and in A. thaliana. In order to independently control the transport of essential and non-essential metals by NRAMP, a study aiming to identify the structural determinants involved in selectivity was undertaken. Expression of NRAMP mutants affected in their selectivity in A. thaliana highlighted their impact on metal accumulation and tolerance. To study the involvement of more general nutrient recycling mechanisms in metal remobilization during leaf senescence, the involvement of autophagy was tested in A. thaliana. Physiological characterization of autophagy deficient plants indicated that this mechanism plays a role in metal use efficiency and probably in metal remobilization during senescence. By combining a field approach on poplar and molecular genetics in Arabidopsis, this work opens multiple perspectives to specifically reduce the accumulation of TE in poplar leaves.

Mutations in the eukaryotic integral membrane protein Cystic Fibrosis Transmembrane conductance Regulator (CFTR) cause the hereditary disease cystic fibrosis (CF). CFTR functions as an ion channel at the surface of epithelial cells and regulates the movement of chloride ions and water across the plasma membrane. CFTR is difficult to express and purify in heterologous systems due to its propensity to form insoluble aggregates and its susceptibility to degradation. Obtaining good yields of highly purified CFTR has proven problematic and contributes to our limited understanding of the structure and function of the protein. The most prevalent disease causing mutation, F508del, results in misfolded CFTR which is particularly unstable and is quickly targeted for degradation by the host system and is prevented from being trafficked to the plasma membrane. There are limited treatment options for patients with the F508del mutation and it is therefore of significant interest within CF research. New methods and assays are required to identify potential compounds which could correct the F508del mutation. This thesis investigates the use of Saccharomyces cerevisiae to express and purify codon optimised recombinant CFTR. The use of a green fluorescent protein (GFP) tag enabled quick and simple detection of CFTR in whole cells and after extraction from the plasma membrane. By optimising the culture conditions for CFTR expression and detergent solubilisation conditions, relatively high yields of full-length protein were obtained. When used as a chemical chaperone at the time of inducing CFTR expression, glycerol increased yields of full-length protein. Degradation of CFTR could be limited by inducing expression at an optimal cell density and by harvesting cells within a specific time window. CFTR was extracted by solubilisation in the mild detergent dodecyl-β-D-maltopyranoside (DDM) in the presence of up to 1 M NaCl with up to ~87% efficiency in some cases. Using a gene optimisation strategy in which additional purification tags and a yeast Kozak-like sequence were added, the human CFTR (hCFTR) protein was expressed and purified. Fluorescence microscopy revealed CFTR localisation at the periphery of yeast cells. Immunoaffinity chromatography facilitated by the GFP tag at the C terminus of CFTR produced protein of up to 95% purity. An assessment of the thermal stability of this highly purified CFTR using a fluorescent probe binding assay revealed a denaturation midpoint (Tm) of ~43 degC. The ability of this assay to determine the stability of CFTR is encouraging and there is the potential to further develop it in a high-throughput manner to identify compounds which stabilise the F508del protein and which may hold the key to developing new treatments for CF.

Kurs: Examensarbete i Logistik, 30 hp Författare: Matilda Svensson och Hanna Delius Handledare:Petra Andersson Examinator: Helena Forslund Titel: Framtida förbättringsmöjligheter för kombi- och omlastningsterminaler - En fallstudie på Alvestas kombi- och omlastningsterminal Nyckelord: Kombi- och omlastningsterminaler, intermodala transporter, utnyttjandegrad, interna och externa faktorer   Arbetets syfte är att identifiera och analysera interna och externa faktorer som uppstår på kombi- och omlastningsterminaler samt att analysera hur utbudet på kombi- och omlastningsterminaler kan utvecklas för att möjliggöra ökad utnyttjandegrad.   Arbetet har besvarat tre frågeställningar: <ol type="1">Vilka interna och externa faktorer har lett till att kombi- och omlastningsterminalen i Alvesta inte når önskad utnyttjandegrad?    Interna faktorer: kompetens, typ av gods, lagring, hantering av gods/ej synkroniserat, ej elektrifierade spår, informationshantering, typ av utrustning, ej kontinuerligt flöde, utrymme och markunderlag. Externa faktorer: Lagar, dieselskatt, vägslitageskatt, konjunktur, befolkningsmängd, buller, nya innovationer, IT-system, infrastruktur, Andra kombi- och omlastningsterminaler, leverantörer, kund och lastbil.   <ol type="1">Hur kan kombi- och omlastningsterminaler i Sverige möta externa faktorer i framtiden? I utförandeplanen kom författarna fram till att det är viktigt för kombi- och omlastningsterminaler att inte bara fokusera på intermodal verksamhet. Det är även viktigt att ha ett effektivt IT-system som kan användas och hantera många och komplexa flöden. Järnvägen är lönsam med gods som är tungt och som kan fraktas långa sträckor därför borde kombi- och omlastningsterminaler kolla på möjligheten att transportera gods till andra länder och inte bara inom Sverige. Sedan borde kombi- och omlastningsterminaler kolla på möjligheten att förlänga spåren som finns på terminalen för att kunna hantera längre tåg. Den sista förbättringslaget är att kombi- och omlastningsterminaler borde kolla på att automatisera hanteringen.   Hur kan kombi- och omlastningsterminalen i Alvesta utvecklas, genom att möta identifierade interna faktorer, för att möjliggöra för ökad utnyttjandegrad?   För att öka utnyttjandegraden har författarna till arbetet kommit fram till att Alvestas kombi- och omlastningsterminal borde ha flera transportoperatörer, förbättrad lagerhantering, stuffa containrar, hantera virkespaket, använda cross-docking, hantera farligt gods, utökade öppettider, bättre markunderlag, elektrifierade spår, hantera timmer, implementera ett intermodalt transportsystem, investera i ett lagringstält, automatisering kring hantering och omlastning.

Submitted by Jean Medeiros (jeanletras@uepb.edu.br) on 2016-03-15T13:08:48Z No. of bitstreams: 1 PDF - Rafaella Bastos Leite.pdf: 1326501 bytes, checksum: 57e6fffb3bbe74433cba4f469a5b6545 (MD5) / Approved for entry into archive by Secta BC (secta.csu.bc@uepb.edu.br) on 2016-07-21T21:05:02Z (GMT) No. of bitstreams: 1 PDF - Rafaella Bastos Leite.pdf: 1326501 bytes, checksum: 57e6fffb3bbe74433cba4f469a5b6545 (MD5) / Approved for entry into archive by Secta BC (secta.csu.bc@uepb.edu.br) on 2016-07-21T21:05:12Z (GMT) No. of bitstreams: 1 PDF - Rafaella Bastos Leite.pdf: 1326501 bytes, checksum: 57e6fffb3bbe74433cba4f469a5b6545 (MD5) / Made available in DSpace on 2016-07-21T21:05:12Z (GMT). No. of bitstreams: 1 PDF - Rafaella Bastos Leite.pdf: 1326501 bytes, checksum: 57e6fffb3bbe74433cba4f469a5b6545 (MD5) Previous issue date: 2014-07-30 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES / The keratocystic odontogenic tumor (KOT) stands out among the other odontogenic lesions in view of the potentially aggressive biological behavior and its association in some cases, with the Gorlin syndrome. Some studies have suggested a more aggressive biological behavior for KOTs associated with Gorlin syndrome, compared to isolated KOTs, characterized by greater growth capacity and bone infiltration and higher tendency to recur. The present study aimed to evaluate, descriptively and comparatively, by means of immunohistochemistry, the expression of glucose transporter-1 (GLUT-1) and -3 (GLUT-3) and the angiogenic index (CD34) in isolated primary and recurrent KOTs and in KOTs associated with Gorlin syndrome. The sample was composed by 21 isolated KOTs (14 primary and 7 recurrent) and 14 KOTs associated with Gorlin syndrome. The expression of GLUTs was evaluated in the epithelial component of the lesions, establishing the percentage of immunopositive cells, according to the scores: score 0 (negative), score 1 (≤ 25% of positive cells), score 2 (26% - 50% of positive cells), score 3 (51% - 75% of positive cells), and score 4 (≥ 76% positive cells). For the angiogenic index, the microvessel count (MVC) technique was applied, quantifying the microvessels immunoreactive to anti-CD34 antibody. Regarding the median scores for immunopositivity for GLUT-1 and the angiogenic index, comparisons between groups were performed using the nonparametric Kruskal-Wallis test. For GLUT-3, the data obtained from the evaluation of epithelial expression of this protein were submitted to descriptive statistical analysis. Possible correlations between the scores of immunopositivity for GLUT-1 and angiogenic index in the lesions were evaluated using the Spearman correlation test. The level of significance was set at 5% (p <0.05). The analysis of epithelial GLUT-1 immunoreactivity revealed predominance of score 4 in isolated primary KOTs (n = 9, 64.3%) and in KOTs associated with Gorlin syndrome (n = 8; 57.1%). In isolated recurrent KOTs, it was identified a slightly higher frequency of cases with scores 4 (n = 3; 42.9%) and 2 (n = 2; 28.6%). The nonparametric Kruskal-Wallis test showed no statistically significant difference between groups (p = 0.406). Regarding the GLUT-3, all groups showed higher frequency of negative cases. The few KOTs positive for GLUT-3 were classified as score 1 (≤ 25% of positive cells), showing a low expression of this protein in the epithelial component. The mean number of microvessels was 63.80 in isolated primary KOTs, 61.11 in KOTs associated with the Gorlin syndrome, and 65.88 in isolated recurrent KOTs, without significant differences between groups (p = 0.965). The results of this study suggest that the differences in biological behavior of isolated KOTs and KOTs associated with Gorlin syndrome may not be related to the expression of GLUTs-1 and -3, or to the angiogenic index in the lesions. The high expression of GLUT-1 in KOTs suggests an important role for this protein in glucose uptake by the epithelial cells of these tumors. / O tumor odontogênico ceratocístico (TOC) se destaca entre as demais lesões odontogênicas em virtude do comportamento biológico potencialmente agressivo e por sua associação, em alguns casos, à síndrome de Gorlin. Pesquisas tem sugerido um comportamento biológico mais agressivo para os TOCs associados à síndrome de Gorlin, em comparação aos TOCs isolados, caracterizado por maior capacidade de crescimento e infiltração óssea e maior tendência a recorrência. O presente estudo se propôs a avaliar, descritiva e comparativamente, a imunoexpressão dos transportadores de glicose-1 (GLUT-1) e -3 (GLUT-3) e o índice angiogênico (CD34) em TOCs isolados primários e recorrentes e TOCs associados à síndrome de Gorlin. A amostra foi composta por 21 TOCs isolados (14 primários e 7 recorrentes) e 14 TOCs associados à síndrome de Gorlin. A expressão dos GLUTs foi avaliada no componente epitelial das lesões, estabelecendo-se o percentual de células imunopositivas, de acordo com os escores: escore 0 (negativo), escore 1 (≤ 25% das células positivas), escore 2 (26% - 50% das células positivas), escore 3 (51% - 75% das células positivas) e escore 4 (≥76% das células positivas). Para o índice angiogênico, foi empregada a técnica da contagem microvascular (MVC), quantificando-se os microvasos imunomarcados pelo anticorpo anti-CD34. Em relação às medianas para os escores de imunopositividade para GLUT-1 e para o índice angiogênico, as comparações entre os grupos foram realizadas por meio do teste não paramétrico de Kruskal-Wallis. Para o GLUT-3, os dados obtidos com a avaliação da expressão epitelial desta proteína foram submetidos apenas à análise estatística descritiva. Possíveis correlações entre os escores de imunopositividade para GLUT-1 e o índice angiogênico nas lesões foram avaliadas por meio do teste de correlação de Spearman. O nível de significância foi estabelecido em 5% (p < 0,05). A análise da imunoexpressão epitelial de GLUT-1 revelou predomínio de casos com escore 4 nos TOCs isolados primários (n = 9; 64,3%) e nos TOCs associados à síndrome de Gorlin (n = 8; 57,1%). Nos TOCs isolados recorrentes, foi identificada frequência discretamente maior para os casos com escores 4 (n = 3; 42,9%) e 2 (n = 2; 28,6%). O teste não paramétrico de Kruskal-Wallis revelou ausência de diferença estatisticamente significativa entre os grupos (p = 0,406). Em relação ao GLUT-3, todos os grupos estudados revelaram maior frequência de casos negativos. Os poucos TOCs positivos para GLUT-3 foram classificados como escore 1 (≤ 25% das células positivas), revelando uma baixa expressão desta proteína no componente epitelial. O número médio de microvasos foi de 63,80 nos TOCs isolados primários, 61,11 nos TOCs associados a síndrome de Gorlin e 65,88 nos TOCs isolados recorrentes, sem diferenças significativas entre os grupos (p = 0,965). Os resultados do presente estudo sugerem que as diferenças no comportamento biológico de TOCs isolados e TOCs associados à síndrome de Gorlin não foram relacionadas com a expressão de GLUTs-1 e -3 ou com o índice angiogênico (CD34) nas lesões. A alta expressão de GLUT-1 em TOCs sugere um importante papel para esta proteína na captação de glicose pelas células epiteliais destes tumores.