Cleft palate is a common human birth defect caused by any process which interferes with palatogenesis. Studies in Hoxa2 mutant (Hoxa2-/-) mice which exhibit a secondary cleft palate were reported to be due to an abnormal positioning of the tongue which prevents normal palatal shelf fusion to occur. To obtain direct evidence for the importance of Hoxa2 in murine palate development, an in vitro whole organ palatal culture model was developed, eliminating any influences from the tongue. A retroviral gene delivery system was employed, containing either Hoxa2 sense or Hoxa2 antisense cDNA, to respectively enhance or knockdown the expression of Hoxa2 mRNA in the developing palate. <p>Our results show that palatal cultures infected with the lowest titer of Hoxa2 sense virus induce a fusion rate of 72.7%, which is similar to palatal cultures treated with the control virus (81.8%), although fusion rates of 41.2% to 50.0% were observed in palates infected with higher titers. With the antisense virus treated group, a more profound inhibition of the fusion rate was observed (27.7% - 46.1%), which is comparable with the frequency of palatal fusion in Hoxa2-/- mice (44.4%). Additionally, the palatal shelves in both sense and antisense virus treated groups appear to be relatively shorter in length, than those measured in the control group. Interestingly, in the antisense virus treated group, the ratio of the length of the fused portion to the length of palatal shelves appears to be relatively large compared to the control group. Verification and quantification of Hoxa2 mRNA in the developing palate between E12.5 and E15.5 was performed by real-time RT-PCR. Hoxa2 gene expression was observed at all stages studied, with expression being the highest at E12.5 and declining from E13.5. The expression level remained constant from E13.5 through E15.5. These findings demonstrate for the first time that Hoxa2 may play a direct role in murine palate development. Results suggest that both factors (the absence of Hoxa2 gene in the palate causing delayed palatal development, as well as the position of the tongue) appear to act in unison to produce cleft palate in Hoxa2 knockout mice.

Branchial arches (BAs) are a series of transient structures that develop on the ventro-lateral surface of the head in vertebrate embryos. BAs initially appear as a series of similar segments; as development proceeds each BA will contribute to different structures. Here, it was investigated the transcriptional mechanisms that instruct the different fates of the BAs in development. Initially, each BA contains a blood vessel, known as aortic arch (AA) artery, that connects the dorsal aorta with the heart. Remodelling of the AAs is crucial to form the adult heart circulation. This process leads to regression of the anterior AAs, running though the first and second BAs (BA1 and BA2), and persistence of the AAs contained in more posterior BAs (PBA). To identify the mechanisms that control remodelling of the AAs, we compared the transcriptomes and epigenomic landscapes of different BAs. Using RNA-seq and H3K27Ac ChIP-seq, we uncovered the activation of a vascular smooth muscle cell (VSMC) differentiation transcriptional program exclusively in the PBAs (and not in BA1/BA2). In support of this finding, we show that VSMC differentiation occurs specifically in the PBAs, but not BA1-2 in mouse embryonic development. Despite the absence of VSMC differentiation in developing BA1-2, cells harvested from these tissues reveal a spontaneous tendency to differentiate towards VSMC fate when grown in vitro, and activate several VSMC-specific genes (Myocd, Acta2, Tagln, Jag1). Together, our results suggest that forming VSMCs is a key process for the persistence of AAs. We also showed that cells derived from all BAs have the potential to differentiate to VSMCs in vitro. However, only cells in the PBAs differentiate to VSMCs in vivo, resulting in the maintenance of posterior AAs. In this study, we also uncovered a novel transcriptional principle that specifies the fate of BA2. Using ChIP-seq, we found that binding of Meis transcription factors establish a ground pattern in the BAs. Hoxa2, which specifies BA2 identity, selects a subset of Meis-bound sites. Meis binding is strongly increased at these sites, which coincide with active enhancers, linked to genes highly expressed in the BA2 and regulated by Hoxa2. Thus, Hoxa2 modifies a ground state binding of Meis to instruct segment-specific transcriptional programs.

Many tropical aquatic environments worldwide are characterized by intermittent or prolonged hypoxia (low dissolved oxygen). Nevertheless, many tropical freshwater fishes are able to inhabit these challenging environments via a range of morphological, physiological and behavioral adaptations. Brachyhypopomus is a diverse genus of weakly electric fishes represented by 28 known species distributed from Panama to Argentina. 17 species are restricted to permanently normoxic habitats (blackwater rivers and terra firme streams), eight species are restricted to seasonally or perennially hypoxic habitats (whitewater floodplains of large tropical rivers or permanent swampy habitats), and three species are eurytopic (occur in both seasonally hypoxic and normoxic habitats). These habitat distributions offer the opportunity to explore both species- and population-level variation in adaptive responses to hypoxia. Across 25 of the 28 known species in the genus (for which specimens were available), one- and two-way ANOVA was used to correlate total gill filament length (a metric of gill surface area) with lifestyle-divided into four categories: 1) stenotopic species (i.e. species occurring in a narrow range of habitats) restricted to hypoxic habitats; 2) stenotopic species restricted to normoxic habitats; 3) populations of eurytopic species from hypoxic habitats, and; 4) populations of eurytopic species from normoxic habitats. One-way ANOVA revealed that populations of eurytopic species from hypoxic habitats had significantly larger total gill filament lengths than stenotopic species from the same habitat (P = 0.0169). Likewise, populations of eurytopic from normoxic habitats had significantly larger total gill filament lengths than stenotopic species from normoxic habitats (P[less than] 0.005). Two-way ANOVA showed that eurytopic species had significantly larger total gill filament lengths than stenotopic species, independent of the disparity in total gill filament length associated with either hypoxic or normoxic habitats. Results indicate a strong correlation between gill surface area and oxygen-habitat among species and populations, which supports the hypothesis that an enlarged gill surface area increases oxygen uptake and serves as an adaptive response to seasonal hypoxia.

Thesis (Ph. D.) -- University of Texas Southwestern Medical Center at Dallas, 2003. / Vita. Bibliography: References located at the end of each chapter.

Thesis (Ph. D.) -- University of Texas Southwestern Medical Center at Dallas, 2003. / Vita. Bibliography: References located at the end of each chapter.

Made available in DSpace on 2016-06-02T19:29:17Z (GMT). No. of bitstreams: 1 2471.pdf: 5609066 bytes, checksum: 5eb83354923bf2ef6bb644d15b85bbd2 (MD5) Previous issue date: 2009-06-05 / Universidade Federal de Sao Carlos / Aluminium is very toxic to fish. Biomarkers have been using to indicate water contamination, however, there are few studies concerning tropical fish species. So, the neotropical fish Prochilodus lineatus, were exposed to aproximately 200 &#956;g.L-1 of dissolved Al em acid pH (Al group), only to acid water (pH group) or to water with pH 7.0 (CTR group) for 6, 24, 96h and 10 days to evaluate its effects on haematological, osmo-ionic, metabolic and endocrine parameters besides morphological analysis by light and electronic microscopy. Fishes exposed to Al have all haematological and metabolic parameters increased when compared to CTR group. Osmo-ionic parameters were significantly smaller in fishes exposed to Al as much as the Na+/K+-ATPase enzyme and the CC number smaller Light microscopy reveal that fish exposed to Al in all experimental periods showed lesions widely distributed in the tissue and considered more severe when compared to fish from other groups. In the Al group, the main alterations found were hyperplasia of the epithelial cells, lamellar fusion and hypertrophy of mucous cells. In the animals of pH group, the main alteration was hipertrophy of epithelial cells, especially of the CC. Scanning electron microscopy allowed to see great disorganization in the lamellae of the fishes exposed to Al, detachment of branchial epithelium and reduction of the interlamellar space. Chloride cells with sponge aspect were noted in the pH and Al groups, besides alteration in the microcript of the pv in both groups. Transmission electron microscopy showed that animals from Al group have more CC displaced to the tip of the lamellae and that these CC have a less dense cytoplasm, with a smaller quantity of tubules and mitochondrias and nuclei with altered shapes. The thickness of the lamellae is bigger because of the swollen pv and the interlamellar spaces are reduced. There are, also, more vacuoles in the cytoplasm of these CC. Results allowed to conclude that exposure to Al in acid medium impairs mostly the hyperegulation capacity of the fish, since it affects the active uptake of ions in the gills and also caused serious structural alterations in the organ, leading to functional problems, jeopardizing the survival of the fishes in such situation. / O alumínio é muito tóxico para os peixes. Biomarcadores tem sido usados para indicar essa contaminação, entretanto são poucos os trabalhos com espécies tropicais. Assim, juvenis do peixe neotropical Prochilodus lineatus foram expostos a aproximadamente 200 &#956;g.L-1 de Al dissolvido em pH ácido (grupo Al), somente pH ácido (grupo pH) ou à água com pH 7,0 (grupo CTR) por 6, 24, 96h e 10 dias para avaliar seus efeitos em parâmetros hematológicos, osmo-iônicos, metabólicos e endócrino, além dos parâmetros morfológicos, por meio de MO, MEV, MET, AFCC e EDS das brânquias. Os peixes expostos ao Al tiveram os parâmetros hematológicos e metabólicos aumentados em relação ao grupo CTR. Os parâmetros osmo-iônicos foram significativamente menores nesses peixes assim como a enzima Na+/K+-ATPase e o número de CC nos mesmos animais. A MO revelou que os peixes expostos ao Al mostraram lesões mais amplamente distribuídas nas brânquias e consideradas mais severas, quando comparados aos demais grupos, sendo que as principais alterações foram hiperplasia do epitélio branquial, fusão lamelar e hipertrofia das células mucosas. Nos animais expostos ao pH a principal alteração foi a hipertrofia celular, principalmente das CC. A MEV permitiu destacar o extenso desarranjo nas lamelas dos peixes dos grupos Al, descamação do epitélio além da redução do espaço interlamelar e fusão lamelar. CC com aspecto esponjoso foram notadas nos grupos pH e Al além da alteração no padrão das microcriptas das célula pv em ambos os grupos. Animais expostos ao Al mostraram ainda AFCC menores em relação aos CTR e o EDS indicou picos de Al maiores nesses grupos. A MET mostrou que os animais expostos ao Al têm mais CC deslocadas para as pontas das lamelas e que essas células apresentam o citoplasma menos denso, com uma menor quantidade de túbulos e mitocôndrias e núcleos formas alteradas, além de mais vacúolos. A espessura das lamelas é maior devido ao inchaço das pv, reduzindo o espaço interlamelar. Os resultados permitiram concluir que exposições ao Al em meio ácido prejudicam principalmente a capacidade de hiperregulação dos peixes afetando a tomada ativa de íons nas brânquias além de sérias alterações estruturais nas brânquias, comprometendo a sobrevivência dos animais nessas situações.

Objetivo Avaliar os efeitos do tabagismo sobre o sistema cardiovascular, através de metodologia não invasiva, analisando as alterações hemodinâmicas clínicas e propriedades elásticas arteriais, após exposição ao fumo. Métodos Estudo realizado em 45 voluntários sendo 18 (F) e 27 (M), fumantes T (n = 25, idade 40 ± 9 anos) e não fumantes NT (n = 20, idade 39 ± 9 anos), que foram submetidos a determinação do monóxido de carbono (CO) e avaliação das propriedades elásticas arteriais por ultrassonografia e teste de função endotelial (hiperemia reativa - HR) antes (B1) e após (B2) a exposição por 20 minutos a um cigarro ou à degustação de uma bala. Resultados Os grupos NT e T mostraram-se homogêneos. A concentração de CO no grupo T era maior do que no grupo NT em condições basais. A concentração de CO no grupo NT não variou antes e após à exposição proposta (bala) mas no grupo T aumentou de maneira significante após o cigarro. A pressão arterial sistólica (PAS) foi igual no B1 nos dois grupos, mas significativamente maior no B2 para o Gr T. A pressão arterial diastólica (PAD) no B1 e B2 não mostrou variação estatísticamente significante nos dois grupos. A freqüência cardíaca (FC) apresentou comportamento estatisticamente diferente nos dois grupos (NT apresentou redução e T apresentou aumento). Em relação às propriedades elásticas arteriais e resposta do fluxo regional: a complacência e a distensibilidade já se mostraram diferentes (p < 0,001) no período basal sendo maior no grupo NT comparado ao grupo T; mas após a HR 1 e 2, o grupo T mostrou elevação estatísticamente significante destas duas propriedades, sendo que o grupo NT não mostrou tais achados. O diâmetro máximo da artéria braquial mostrou-se aumentado em relação ao basal tanto após HR1 como após HR2 apenas no grupo T. O índice de fluxo total (IFT) não era diferente nos dois grupos no B1 e B2, mas após HR 1 e 2 ambos mostraram aumentos significantes (p < 0,001). Houve correlação positiva entre variáveis CO com PAD e FC no grupo T. No grupo NT não houve correlação do CO com PAS, PAD ou FC. Conclusão O tabagismo altera as propriedades elásticas das artérias e tem papel na hemodinâmica com provável participação do monóxido de carbono. / Objective to evaluate the effects of cigarette smoking on cardiovascular system, with non-invasive methodology, analysing hemodynamic disturbs and arterial elastic properties after being exposed to tobacco. METHODS This study was realized in 45 volunteers, 18 female and 27 male smokers T (n=25, age 40 ± 9 years) and non-smokers NT (n=20, age 39 ± 9 years), who were submitted to the determination of carbon monoxide (CO) to the evaluation of the arterial elastic properties by ultrassonography and test endotelial function (reactive hyperemia - HR) before (B1) and after (B2) the exposition for 20 minutes to a cigarette or a candy. RESULTS Both NT and T groups were similar.The CO concentration in the T group was higher than in the NT group on basal conditions. The CO concentration in the NT group have not changed before and after the proposed exposition (candy) but in the T group it was significant in creased after the cigarette exposition.The systolic blood pressure (PAS) was similar on B1 for both groups, but it was significantly higher on B2 for the T group. The diastolic blood pressure (PAD) on B1 and B2 didn´t exposition significant statistical variation on both groups. The cardiac frequency (FC) presented a different result for both groups with statistical significance ( NT had decrease and T had improved). Regarding the arterial elastic properties and the regional flux response: the complacence and the distensibility were different (p < 0,001) in the basal period and they were higher in the NT group compared to the T group. After HR 1 and 2, the T group showed a significant statistical increase of those two properties and the NT group didn´t show those results. The righest diameter of the brachial artery was increased in relation to the basal diameter after HR1 as well as after HR2 only in the T group. The total flux index (IFT) were not different in both groups in B1 and B2, but after HR1 and 2 both showed significant increase (p < 0,001). There was a positive correlation between the CO variations in relation to PAD and FC in the T group. In the NT group there was a no correlation of CO with PAS, PAD or FC. CONCLUSION Cigarette smoking changes the arterial elastic properties and it has a role in the hemodynamic with possible participation of the carbon monoxide

Objetivo Avaliar os efeitos do tabagismo sobre o sistema cardiovascular, através de metodologia não invasiva, analisando as alterações hemodinâmicas clínicas e propriedades elásticas arteriais, após exposição ao fumo. Métodos Estudo realizado em 45 voluntários sendo 18 (F) e 27 (M), fumantes T (n = 25, idade 40 ± 9 anos) e não fumantes NT (n = 20, idade 39 ± 9 anos), que foram submetidos a determinação do monóxido de carbono (CO) e avaliação das propriedades elásticas arteriais por ultrassonografia e teste de função endotelial (hiperemia reativa - HR) antes (B1) e após (B2) a exposição por 20 minutos a um cigarro ou à degustação de uma bala. Resultados Os grupos NT e T mostraram-se homogêneos. A concentração de CO no grupo T era maior do que no grupo NT em condições basais. A concentração de CO no grupo NT não variou antes e após à exposição proposta (bala) mas no grupo T aumentou de maneira significante após o cigarro. A pressão arterial sistólica (PAS) foi igual no B1 nos dois grupos, mas significativamente maior no B2 para o Gr T. A pressão arterial diastólica (PAD) no B1 e B2 não mostrou variação estatísticamente significante nos dois grupos. A freqüência cardíaca (FC) apresentou comportamento estatisticamente diferente nos dois grupos (NT apresentou redução e T apresentou aumento). Em relação às propriedades elásticas arteriais e resposta do fluxo regional: a complacência e a distensibilidade já se mostraram diferentes (p < 0,001) no período basal sendo maior no grupo NT comparado ao grupo T; mas após a HR 1 e 2, o grupo T mostrou elevação estatísticamente significante destas duas propriedades, sendo que o grupo NT não mostrou tais achados. O diâmetro máximo da artéria braquial mostrou-se aumentado em relação ao basal tanto após HR1 como após HR2 apenas no grupo T. O índice de fluxo total (IFT) não era diferente nos dois grupos no B1 e B2, mas após HR 1 e 2 ambos mostraram aumentos significantes (p < 0,001). Houve correlação positiva entre variáveis CO com PAD e FC no grupo T. No grupo NT não houve correlação do CO com PAS, PAD ou FC. Conclusão O tabagismo altera as propriedades elásticas das artérias e tem papel na hemodinâmica com provável participação do monóxido de carbono. / Objective to evaluate the effects of cigarette smoking on cardiovascular system, with non-invasive methodology, analysing hemodynamic disturbs and arterial elastic properties after being exposed to tobacco. METHODS This study was realized in 45 volunteers, 18 female and 27 male smokers T (n=25, age 40 ± 9 years) and non-smokers NT (n=20, age 39 ± 9 years), who were submitted to the determination of carbon monoxide (CO) to the evaluation of the arterial elastic properties by ultrassonography and test endotelial function (reactive hyperemia - HR) before (B1) and after (B2) the exposition for 20 minutes to a cigarette or a candy. RESULTS Both NT and T groups were similar.The CO concentration in the T group was higher than in the NT group on basal conditions. The CO concentration in the NT group have not changed before and after the proposed exposition (candy) but in the T group it was significant in creased after the cigarette exposition.The systolic blood pressure (PAS) was similar on B1 for both groups, but it was significantly higher on B2 for the T group. The diastolic blood pressure (PAD) on B1 and B2 didn´t exposition significant statistical variation on both groups. The cardiac frequency (FC) presented a different result for both groups with statistical significance ( NT had decrease and T had improved). Regarding the arterial elastic properties and the regional flux response: the complacence and the distensibility were different (p < 0,001) in the basal period and they were higher in the NT group compared to the T group. After HR 1 and 2, the T group showed a significant statistical increase of those two properties and the NT group didn´t show those results. The righest diameter of the brachial artery was increased in relation to the basal diameter after HR1 as well as after HR2 only in the T group. The total flux index (IFT) were not different in both groups in B1 and B2, but after HR1 and 2 both showed significant increase (p < 0,001). There was a positive correlation between the CO variations in relation to PAD and FC in the T group. In the NT group there was a no correlation of CO with PAS, PAD or FC. CONCLUSION Cigarette smoking changes the arterial elastic properties and it has a role in the hemodynamic with possible participation of the carbon monoxide