Banca: Horacio Faig Leite / Banca: Yasmin Rodarte Carvalho / Banca: Suzana Catanhede Orsini Machado de Sousa / Banca: Fabio Daumas Nunes / Banca: Décio dos Santos Pinto Junior / Resumo: O modelo de câncer bucal em hamsters exibe muitas semelhanças com o desenvolvimento do câncer oral em humanos. A capacidade proliferativa é uma das principais características das células neoplásicas e a detecção de células proliferativas permite, através de sua contagem, obter uma estimativa das taxas de crescimento neoplásico, com consequente repercussão no prognóstico e no tratamento das lesões. Foram utilizados 40 hamsters Sírios dourados, machos e fêmeas, com peso aproximado de 150 gramas, com dois a seis meses de idade. A seguir, foi aplicada solução de DMBA na borda lateral esquerda da língua dos animais por oito semanas. Os animais foram sacrificados, e as línguas removidas foram fixadas em formei tamponado a 10%. O cortes histológicos foram corados pela prata para marcação das NOR e pelos anticorpos PCNA e β-catenina. Os dados obtidos receberam tratamento estatístico pelo teste ANOVA e teste de Tukey. Após análise dos resultados pudemos concluir que as associações da técnica pelo AgNOR e a imunoistoquímica pelo PCNA refletiram a maior atividade proliferativa das células analisadas. O modelo de carcinogênese experimental em borda lateral de língua de hamster é uma metodologia que se presta para estudo por imunoistoqufmica. E finalmente, que os anticorpos PCNA e β-catenina podem ser utilizados, nos casos leucoplasia, para analisar possíveis áreas de transformação maligna / Abstract: The oral cancer model in hamsters shows many simílarities with developmental oral cancer in humans. The proliferating capacity is one the most characteristics of neoplásica ce/Is and detection of these ce/Is allow us, throughout of its counting, to achieve an estimated tumour growing index, with a consequent repercussion about prognostic and in the treatment of those lesions. 40 golden Syrian hamsters, both genders, aged between two to six mouth and weight 150g in average were used. The left síde of tangue of each animal was painted for eight consecutive weeks, with a solution of DMBA. Tongues were removed, fixed in 10% buffered fonnal solution. The histological slides were stained by AgNOR technique and by PCNA and β-catenin immunohistochemical antibodies. Statistical analyzes were performed by ANOVA one-way test and Tukey test. We may conclude that an association between AgNOR and PCNA might indicate the higher proliferating activity of the analyzed celIs. The experimental carcinogenesis model in hamster tongue is an available methodology for immunohistochemistry study. And finally, PCNA and β-catenin immunohistochemical antibodies may be used to analyze possible premalignant areas in oral leukoplakia

Conclusion. Taken together, paternal factors carried in ASG secretion affect genomic imprinting of developing embryos. The outcome of research work described here deepens our understanding of the role of ASG in maximizing reproductive performance mediated by regulating the epigenetic marks of the genome and in particular the imprinted genes. / Introduction. Our previous in vivo studies in golden hamster have shown the accessory sex glands (ASG) secretion facilitate the development of embryos to term but the underlying mechanism is still not clear. Since the deleterious effect caused by the lack of sperm exposure to ASG secretion is heritable to developing fetus and even after birth, we hypothesized that the paternal factor carried in ASG secretion may change the epigenetic regulation and in particular the imprinted genes of embryonic genome. / Materials and methods. Golden hamster and ICR mouse were used in this study. Hamster is a well-established animal model to study the effect of individual ASG but the genetic background of hamster is poorly known. To verify the specificity of our molecular probe and antibodies used in hamster, a mouse model was also established. Five groups of male hamsters and two groups of male mice were established by surgical treatment. In hamster, (SH) sham-operated, (VPX) ventral prostate-removed, (TX) all ASG-removed, (VPVX) castrated with ASG-removed except ventral prostate and (VX) castrated with intact ASG were established. In mouse, SH and VPX were established. In single-mating of hamster, male was copulated with female at estrus for 15 min. In double-mating of hamsters, female mated with each male for 10 min each. In single-mating of mouse, male was caged with female for 1 h. Epididymal sperm, uterine sperm, fertilized oocytes, pre-implantation embryos and fetuses at 13 days gestation (E13) were collected. Global DNA methylation of sperm, fertilized oocytes, early embryos and E13 fetuses were investigated by indirect immunofluorescence and DNA dot-blot using antibody against methylated DNA. Using the same technique, histone acetylation at lysine 5 residue was detected in male pronuclei of fertilized oocytes, protamine 1 and 2 content were detected in sperm, DNA methyltransferase 1, 3a and 3b activities were detected in early embryos. The crown-rump length and weight of fetuses were measured. Morphology was also examined under scanning electron microscope. Two sets of co-ordinately regulated but oppositely expressed imprinted genes Igf2/H19 and Dlk1/Gtl2 were investigated. H19 differentially methylated region (DMR) and Gtl2 promoter were examined by bisulfite sequencing in sperm and E13 fetuses. Expression of Igf2 and Dlk1 were examined by in situ hybridization and real-time PCR in pre-implantation embryos and E13 fetuses. / Results. Uterine sperm in VPX and TX groups showed no change of DNA methylation level and protamine 1 and 2 content. Fertilized oocytes in VPX and TX groups showed similar DNA methylation level as SH group in both hamster and mouse. Histone hypoacetylation was observed in male pronuclei of hamster but not in mouse. Early embryos in VPX and TX groups showed abnormal level of DNA methylation and Dnmt3b during embryo development in hamster. Replenishment of ASG secretion to sperm from VPX and TX group by double-mating restored the DNA methylation level to normal in early embryos. E13 fetuses of VPX and TX groups in hamster and VPX group in mouse showed DNA hypomethylation. E13 fetuses of VPX group in hamster showed increase in average crown-rump length and body weight with larger variations between individuals. One E13 fetus of VPX group in mouse showed polydactyly and malformation in the head. Real-time PCR showed abnormal expression of Igf2 and Dlk1 in both pre-implantation embryos and E13 fetuses of VPX and TX groups. Bisulfite sequencing showed hypermethylation of H19 DMR in VPX and TX groups of hamster and hypomethylation of Gtl2 promoter in VPX group of mouse. / "August 2007." / Adviser: Pak Ham Chow. / Source: Dissertation Abstracts International, Volume: 69-08, Section: B, page: 4739. / Thesis (Ph.D.)--Chinese University of Hong Kong, 2007. / Includes bibliographical references (p. 194-224). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstract in English and Chinese. / School code: 1307.

Made available in DSpace on 2014-06-11T19:30:57Z (GMT). No. of bitstreams: 0 Previous issue date: 2007-03-08Bitstream added on 2014-06-13T21:01:42Z : No. of bitstreams: 1 pedrini_scb_dr_botfm.pdf: 905602 bytes, checksum: e7f0ba6f8ec19cb6910c250e4ca919fe (MD5) / A hanseníase é, ainda hoje, um problema global de saúde pública. O Brasil e a Índia são os países com maior prevalência da doença. A existência de tatus Dasypus novemcinctus naturalmente infectados por Mycobacterium leprae foi relatada nos Estados Unidos, México, Argentina e no Brasil, no Estado do Espírito Santo. Micobactérias potencialmente patogênicas e algumas ambientais já foram isoladas destes animais. A identificação do bacilo é dificultada, particularmente pela sua incapacidade de crescimento in vitro. Portanto, o uso de ferramentas moleculares representa uma alternativa mais rápida e sensível para diagnóstico de micobacterioses. Neste trabalho foram feitas baciloscopia, cultura e PCR com primers específicos para seqüências repetitivas de M. leprae, a partir de DNA extraído de amostras de fígado, baço, linfonodos e pele de 21 tatus D. novemcinctus, Euphractus sexcintus e Cabassous tatouay provenientes da região Centro-Oeste do Estado de SP, dos quais 17 eram provenientes do Banco de DNA do Laboratório de Biologia de Fungos do Departamento de Microbiologia e Imunologia - IBB. Para a padronização da metodologia foram utilizados hamsters experimentalmente infectados por M. avium e o modelo experimental para hanseníase (D. novemcinctus) do Biotério de Experimentação Animal do Instituto Lauro de Souza Lima, Bauru-SP. Com exceção de dois tatus, cujas amostras fezes foram positivas pela PCR, nenhum tatu selvagem apresentou infecção natural por micobactérias. Somente o tatu inoculado com biópsia de paciente virchowiano foi positivo, tanto na PCR, quanto no seqüenciamento genômico, que revelou 100% de identidade com o M. leprae. Os resultados preliminares deste estudo, com base na metodologia empregada, sugerem que existe um indicativo de que os tatus selvagens podem apresentar papel de reservatório de M. leprae na cadeia epidemiológica da doença, na região estudada. / Leprosy is still a worldwide public health problem. Brazil, in addition to India, show the highest prevalence rates of the disease. Natural infection of armadillos Dasypus novemcinctus with Mycobacterium leprae has been reported in the United States, Mexico, Argentina and Brazil, in the State of Espírito Santo. Potentially pathogenic and ambiental mycobacteria have been isolated from these animals. Identification of bacilli is difficult, particularly because its inability to grow in vitro. The use of molecular tools represent a fast and sensitive alternative method for diagnosis of mycobacteriosis. In the present study, the diagnostic methods used were bacilloscopy, culture and PCR using specific primers for M. leprae repetitive sequences. The PCR were performed using genomic DNA extracted from liver, spleen, lymphnodes and skin of 21 D. novemcinctus, Euphractus sexcintus and Cabassous tatouay armadillos from the Middle Western region of the State of São Paulo. From those, 17 samples were taken from the DNA Bank of the Fungal Biology Laboratory at Department of Microbiology and Immunology IB - Botucatu, UNESP. Standardization of the technique was done in M. avium experimentally infected hamsters and M. leprae experimentally infected D. novemcinctus tissue from the Laboratory Animal House at Instituto Lauro de Souza Lima, Bauru-SP. No one of the wild armadillos showed natural mycobacterial infection. Only the armadillo inoculated with material collected from untreated multibacillary leprosy patient was PCR positive. The genomic sequencing revealed 100% identity with M. leprae. According to these preliminary studies, based on the methodology, we may conclude that wild armadillos seem play a role on epidemiology of leprosy in the Middle Western region of the State of São Paulo.

A proteomics approach was used to identify proteins potentially implicated in the cellular response concurrent with elevated production levels of human follicle stimulating hormone in a recombinant Chinese hamster ovary cell line (Darren cells), using zinc and sodium butyrate in the production media to increase expression. To this end, 2-dimensional gel electrophoresis (2-DGE) was utilized. Firstly, several aspects of 2-DGE were developed for this investigation. Gel drying conditions were optimized, and a glycine-free blotting method is described which achieved greater efficiency in rapid transfer of proteins than those previously described. Next, hFSH expression was characterized in Darren cells. An ELISA developed for this investigation examined intracellular (expression) and extracellular (secretion) of hFSH during increased expression. These results show a disproportionate increase in intracellular hFSH (188%) expression above extracellular hFSH (41%).

Most glyco-engineering approaches used to improve quality of recombinant glycoproteins involve the manipulation of glycosyltransferase and/or glycosidase expression. We investigated whether the over expression of nucleotide sugar transporters, particularly the CMP-sialic acid transporter (CMP-SAT), would be a means to improve the sialylation process in CHO cells. We hypothesized that increasing the expression of the CMP-SAT in the cells would increase the transport of the CMP-sialic acid in the Golgi lumen, hence increasing the intra-lumenal CMP-sialic acid pool, and resulting in a possible increase in sialylation extent of proteins being produced. We report the construction of a CMP-SAT expression vector which was used for transfection into CHO-IFNγ, a CHO cell line producing human IFNγ. This resulted in approximately 2 to 5 times increase in total CMP-SAT expression in some of the positive clones as compared to untransfected CHO-IFNγ, as determined using real-time PCR analysis. This in turn concurred with a 9.6% to 16.3% percent increase in site sialylation. This engineering approach has thus been identified as a novel means of improving sialylation in recombinant glycoprotein therapeutics. This strategy can be utilized feasibly on its own, or in combination with existing sialylation improvement strategies. It is believed that such multi-prong approaches are required to effectively manipulate the complex sialylation process, so as to bring us closer to the goal of producing recombinant glycoproteins of high and consistent sialylation from mammalian cells. / Singapore-MIT Alliance (SMA)

In the field of biologics production, productivity and stability of the transfected gene of interest are two very important attributes that dictate if a production process is viable. To further understand and improve these two traits, we would need to further our understanding of the factors affecting them. These would include integration site of the gene, gene copy number, cell phenotypic variation and cell environment. As these factors play different parts in the development process, they lead to variable productivity and stability of the transfected gene between clones, the well-known phenomenon of “clonal variation”. A study of this phenomenon and how the various factors contribute to it will thus shed light on strategies to improve productivity and stability in the production cell line. Of the four factors, the site of gene integration appears to be one of the most important. Hence, it is proposed that work is done on studying how different integration sites affect the productivity and stability of transfected genes in the development process. For the study to be more industrially relevant, it is proposed that the Chinese Hamster Ovary dhfr-deficient cell line, CHO-DG44, is used as the model system. / Singapore-MIT Alliance (SMA)

Lawsonia intracellularis causes proliferative enteropathies in juvenile mammals. The porcine (PPE) and equine (EPE) diseases are worldwide. Rabbits and hamsters are naturally susceptible, the latter being a classic modeling-host for PPE. None is known for EPE, besides foals. An in vitro evaluation of antimicrobial efficacy against L. intracellularis is difficult. This study aimed to validate a laboratory animal EPE model and to investigate pharmacokinetics (PK) and efficacy of gallium maltolate (GaM) as an alternative antimicrobial therapy. Infected animals were inoculated with cell-cultured L. intracellularis and infection was verified with clinically utilized diagnostic tests. Initially, 2 groups of EPE-infected rabbits were compared to 1 uninfected group. After inoculation (PI), EPE-infected rabbits showed mild clinical signs; detectable seroconversion, fecal shedding, gross lesions in intestinal tissues (IT), and early immuno-histochemistry labeling of L. intracellularis antigen. Thus, a humane EPE-rabbit model was achieved. Subsequently, EPE-infected hamsters were compared to uninfected and PPE-infected hamsters; whereas, PPE-infected rabbits were compared to EPE-infected rabbits. EPE-hamsters did not develop infection, unlike PPE-infected controls; and PPE-rabbits did not develop IT lesions or seroconversion comparable to EPE-rabbits. Therefore rabbits were chosen as the EPE modeling-host for the GaM studies. First, GaM PK and IT concentrations of Ga and Fe were measured. Then, GaM efficacy was compared to a current EPE antimicrobial treatment. During sampling, the intra-arterial catheters in the rabbits’ ears were protected with a novel moleskin-cover, allowing repeated sampling while minimally restrained. The PK study was based on the comparison of EPE-infected and uninfected rabbits, after a single treatment with GaM, collection of serial blood samples and IT samples. The only differing PK parameter, between groups, was a decrease in the terminal phase rate constant of the EPE-rabbits, so a 48h dosing interval was chosen for the efficacy study. In the efficacy study, 3 groups of EPE-infected rabbits were treated with GaM, doxycycline and a placebo, respectively. No differences were noted between treatments, in terms of lesions and fecal shedding. GaM appears no more efficacious than doxycycline in EPE- rabbits. In conclusion, albeit GaM tolerance appeared adequate in rabbits, results do not support its use in EPE-infected animals.

Adaptive reproductive behavior requires the ability to recognize and approach possible mating partners in the environment. Syrian hamsters (Mesocricetus auratus) provide a useful animal model by which to study the neural processing of sexual signals, as mate recognition in this species relies almost exclusively on the perception of social odors. In the laboratory, male hamsters prefer to investigate female odors compared to male odors, and this opposite-sex odor preference provides a sensitive measure of the underlying neural processing of sexual stimuli. In addition to chemosensory cues, reproductive behavior in hamsters also requires sufficient levels of circulating gonadal steroid hormones, which reflect the reproductive state of the animal. These chemosensory and hormone signals are processed within an interconnected network of ventral forebrain nuclei, and within this network, the posteromedial cortical amygdala (PMCo) and medial amygdala (MA) are the only nuclei that both receive substantial chemosensory input and are also highly sensitive to steroid hormones. Although a large body of evidence suggests that the MA is critical for generating attraction to sexual odors, the specific role of the PMCo in regulating odor-guided aspects of male reproductive behavior has never been directly tested. Furthermore, detailed analyses of the MA suggest that separate, but interconnected sub-regions within this nucleus process odors differently. Specifically, the anterior MA (MeA) receives the majority of chemosensory input and responds to a variety of social odors, whereas the posterodorsal MA (MePD) receives less chemosensory input but contains the vast majority of steroid receptors. In order to further elucidate how the PMCo and/or MA process sexual odors, this dissertation addressed the following research questions: (1) Is the PMCo required for the expression of either opposite-sex odor preferences or male copulatory behavior? (2) Are functional interactions between MeA and MePD required for the expression of opposite-sex odor preferences? (3) How do MeA and MePD regulate odor responses within the MePD and MeA, respectively? (4) Are odor and/or hormone cues conveyed directly between MeA and MePD? Together, these experiments provide a comprehensive analysis of the functional and neuroanatomical substrates by which the brain processes sexual odors and generates appropriate behavioral responses to these stimuli.

Stress affects virtually all organisms and can result in both physiological and behavioral changes. Conditioned defeat in Syrian hamsters is a model of stress-induced behavioral plasticity that occurs in a social context. In this model, hamsters are defeated by a larger, more aggressive counterpart. Defeated hamsters subsequently fail to defend their own territory and show striking and long-lasting increases in submissive behavior even when paired with a non-threatening counterpart. The present series of experiments seeks to identify the brain regions and molecular mediators that contribute to this behavioral plasticity. One brain region that has been overlooked by our laboratory is the hippocampus. The results of the first study suggested that the ventral, but not dorsal, hippocampus is important for the acquisition of conditioned defeat as temporary inactivation of the ventral hippocampus prior to defeat training significantly reduced submissive and defensive behaviors when hamsters were tested with a non-aggressive intruder. Next, we sought to identify a potential molecular mediator of social stress-induced behavioral plasticity in hamsters identified as winners or losers after a fight. Using in situ hybridization for brain-derived neurotrophic factor (BDNF) mRNA, we showed that winning and losing hamsters exhibited differences in BDNF mRNA in several regions including the basolateral and medial amygdala as well as the dentate gyrus of the dorsal hippocampus and CA1 of the ventral hippocampus. We next showed that neurotrophic activity in the basolateral amygdala is important for the acquisition of conditioned defeat because K252a infused into the basolateral amygdala prior to defeat training by an aggressive counterpart, significantly decreased submissive and defensive behavior during subsequent testing. Finally, existing data suggest that the amygdala and hippocampus interact to modulate the formation of emotional memories. To test the hypothesis that the basolateral amygdala and ventral hippocampus interact to mediate the behavioral plasticity observed in conditioned defeat, we simultaneously inactivated these regions either contralaterally or ipsilaterally prior to social defeat. Our results suggest that BLA and VHPC interact to mediate the acquisition of conditioned defeat, however, the nature of this interaction remains to be determined.

In certain species, puberty is thought to be a period of susceptibility to various stressors, resulting in pathological behavioral and physiological changes subsequent to exposure during this period. However, juvenile male golden hamsters appear to be fairly resilient to pubertal stress, as compared to adult hamsters and many other species. In these experiments, repeatedly stressed juvenile male hamsters were found to be avoidant of aggressive adult male social stimuli, but did not display anxious behavior outside of a social context. In addition, several long-term changes in neural activity were associated with social stress during early puberty. The medial preoptic area and medial preoptic nucleus, and ventral tegmental area showed decreased neural activity in subjugated juveniles than in naïve individuals. Since these brain areas are involved in the expression of motivated behaviors, specifically sexual behavior, and reward pathways, we next investigated sexual behavior in virgin juveniles. When placed in a confined space with receptive females, consummatory behavior in subjugated juveniles was similar to those observed in naive juveniles. Appetitive aspects of sexual behavior were also tested in a Y-maze to allow subjects to choose whether to approach a social stimulus. When given a choice between a sexually receptive and non-receptive female social stimulus, socially stressed individuals showed anxiety related behaviors and did not show a preference. However, naïve hamsters preferred the non-receptive female. Interestingly, this effect was less significant in naïve animals tested during late puberty and early adulthood, and a preference for sexually receptive females was not observed. In addition, stressed hamsters tested with harnessed females at mid-puberty were slower to approach females, indicating altered motivation to approach adult conspecifics. This research is unique in that it is the first to suggest the disconnect between the development of consummatory and appetitive aspects of sexual behavior. Together, these data examine the effects of stress on the development of pubertal social behaviors. / text