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Introdução: o timo é importante órgão linfoide do sistema imunológico. Estudos mostraram que, durante o período fetal, a atrofia desse órgão faz parte da resposta adaptativa do feto ao ambiente intrauterino adverso, como a desnutrição crônica causada pela insuficiência placentária. Essa situação pode explicar a associação entre restrição de crescimento intrauterino e as alterações no sistema imunológico após o nascimento, na infância e na adolescência. Objetivos: analisar as dimensões do timo fetal pela ultrassonografia em gestações com insuficiência placentária, comparando com gestações de alto risco sem insuficiência placentária e gestações de baixo risco. Métodos: estudo prospectivo com 30 gestações com insuficiência placentária (Doppler de artéria umbilical com índice de pulsatilidade > p95) comparadas com 30 de alto risco e 30 de baixo risco (grupo controle). Os critérios de inclusão foram: idade gestacional entre 26 e 37 semanas, feto único e vivo, ausência de malformações fetais, membranas íntegras, ausência de sinais de trabalho de parto, ausência de infecção materna ou fetal e não realização de corticoterapia antes da avaliação ultrassonográfica fetal. O timo fetal foi identificado na interface com os pulmões, na altura dos três vasos da base do coração, no corte do tórax fetal. Foram realizadas três medidas do diâmetro transverso (DT) e do perímetro (P) do timo, e as médias foram utilizadas para análise, transformadas em escores zeta, de acordo com a idade gestacional em que se efetuou a medida. Foram realizadas as medidas ultrassonográficas da circunferência cefálica (CC) e do comprimento do fêmur (CF) fetal, com as quais se calculou as relações DT/CF, DT/CC, P/CF e P/CC. Resultados: o grupo com insuficiência placentária apresentou mediana significativamente maior do escore zeta do IP da artéria umbilical quando comparado ao grupo de alto risco e controle (4,6 vs. -0,5 vs. -0,2, p < 0,001). As medidas do timo fetal no grupo com insuficiência placentária [escore zeta do DT (média=-0,69; DP=0,83) e escore zeta do P (média=-0,73; DP=0,68)] foram significativamente (p < 0,001) menores quando comparadas aos grupos de alto risco [escore zeta do DT (média=0,49; DP=1,13) e escore zeta do P (média=0,45; DP=0,96)] e controle [escore zeta do DT (média=0,83; DP=0,85) e escore zeta do P (média=0,26; DP=0,89)]. Nas relações estudadas, houve diferença significativa (p < 0,05) na média dos grupos: insuficiência placentária (DT/CC=0,10, P/CF=1,32 e P/CC=0,26); alto risco (DT/CC=0,11, P/CF=1,40 e P/CC=0,30) e controle (DT/CC=0,11, P/CF=1,45 e P/CC=0,31). Conclusão: em gestações complicadas pela insuficiência placentária, ocorre redução das dimensões do timo fetal sugerindo que pode ser decorrente da adaptação fetal ao ambiente intrauterino adverso / Introduction: thymus gland is an important lymphoid organ involved in immune response. Studies have shown that during fetal life, thymus atrophy is part of an adaptive response to a compromised intrauterine environment, like chronic malnutrition due to placental insufficiency. This may explain the association between intrauterine growth restriction and later altered immune function. Objective: to evaluate fetal thymus by ultrasonography in pregnancies with placental insufficiency and compare to high risk pregnancies without placental insufficiency and low risk pregnancies. Methods: a prospective study with 30 pregnancies with placental insufficiency (umbilical artery Doppler with pulsatility index > p95), compared to 30 high risk pregnancies and 30 low risk pregnancies (control group). The inclusion criteria were: gestational age ranging from 26 to 37 weeks, singleton pregnancies, absence of fetal malformations, intact membranes, not in labor, no signs of maternal or fetal infection, and no corticotherapy before the ultrasound evaluation. Fetal thymus was identified in its interface with the lungs, at the level of the tree-vessel view of the fetal thorax. Three measures of thymus transverse diameter (TD) and perimeter (P) were made, and the media were converted into zeta score according to the gestational age. Head circumference (HC) and femur length (F) were also measured and used in the calculation of the relations TD/F, TD/HC, P/F, P/HC. Results: the group with placental insufficiency presented median of umbilical artery PI elevated, when compared to high risk pregnancies and low risk pregnancies (4.6 vs. -0.5 vs. -0.2, p < 0.001). Fetal thymus measurements were significantly (p < 0.001) lower in pregnancies with placental insufficiency [TD zeta score (media=-0.69; SD=0.83) and P zeta score (media=-0.73; SD=0.68)] when compared to high risk pregnancies [TD zeta score (media=0.49; SD=1.13) and P zeta score (media=0.45; DP=0.96)] and control group [TD zeta score (media=0.83; SD=0.85) and P zeta score (media=0.26; SD=0.89)]. There was significant difference (p < 0,05) in the relations studied among the groups: pregnancies with placental insufficiency (TD/HC=0.10, P/F=1.32 e P/HC=0.26), high risk pregnancies (TD/HC=0.11, P/F=1.40, P/HC=0.30) and control group (DT/HC=0.11, P/F=1.45, P/HC=0.31). Conclusion: fetal thymus measurements are reduced in pregnancies with placental insufficiency, suggesting that it is a fetal adaptive response for adverse environment

A desnutrição é capaz de induzir diversas alterações metabólicas afetando marcadamente a composição corporal e o sistema imunológico. O exercício físico, por sua vez, produz alterações no organismo para uma melhor capacidade de adaptação a situações de estresse. O desvio da situação de homeostase produzida pelo exercício físico induz uma reorganização de seus mecanismos funcionais, principalmente dos mecanismos endócrinos e imunológicos. Ainda é pouco conhecida a influência do exercício sobre a desnutrição e também as conseqüências sobre o sistema imunológico quando as duas variáveis são combinadas. Assim, esse trabalho teve como objetivo avaliar os efeitos do exercício físico de endurance sobre ratos submetidos a um protocolo de desnutrição crônica. Avaliamos ratos Wistar machos, desnutridos por 16 semanas, divididos em 4 grupos: eutrófico sedentário (ES), eutrófico treinado (ET), desnutrido sedentário (DS), desnutrido treinado (DT). O treinamento físico foi realizado em esteira, por 10 semanas, 5 vezes por semana, com intensidade aproximada de 60- 65% do consumo máximo de oxigênio. Avaliou-se a composição corporal, através da aferição do peso corporal, peso dos tecidos muscular esquelético e adiposo, do fígado, do conteúdo de gordura e proteína na carcaça, e a concentração de leptina, ACTH, glicose, insulina, e glutamina no plasma. Avaliamos também, através de citometria de fluxo, os marcadores de superfície celular CD3 e CD4, bem como a celularidade no timo. O consumo máximo de oxigênio e o desempenho através de um teste até a exaustão também foram analisados. A análise estatística utilizada foi o teste de variância ANOVA two-way com pós teste de Bonferroni e, nível de significância adotado de p<0,05. Os resultados encontrados demonstraram que o treinamento de endurance em ratos submetidos à desnutrição crônica promoveu uma acentuada redução do peso e da adiposidade corporal; um aumento da massa muscular relativa ao peso corporal; um restabelecimento da glicemia aos valores normais; uma melhor relação da concentração insulina/glicose, sugerindo uma sensibilidade à insulina aumentada; um aumento dos estoques de glicogênio muscular; um maior consumo máximo de oxigênio; e uma recuperação na morfologia e fisiologia tímica, uma maior resposta proliferativa do baço e linfonodos estimulados com IL2. Concluímos desta forma que o exercício foi capaz de recuperar a morfologia, como também a maturação timócitos CD3 e CD4 e sua celuraridade em ratos desnutridos. A resposta proliferativa à estimulação da IL2 também foi recuperada. / Malnutrition is capable of inducing diverse metabolic alterations, markedly affecting body composition and the immune system. Physical exercise, on the other hand, induces a renders the organism more capable of adaptation to stress. Still, little is known about the influence of exercise training upon malnutrition-related alterations and its consequences on the immune system. Our aim was to evaluate the effect of moderate intensity exercise training in rats submitted to a protocol (16wk) of chronic malnutrition. Male Wistar rats were divided in to 4 groups: sedentary, fed ad libitum (SF); trained fed ad libitum (TF); sedentary energy restricted (RES); and trained energy restricted (TER). Training was carried out on a treadmill for 10 weeks, 5 time wk, under an intensity of 60-65% of the maximal oxygen consumption. We evaluated the Corporal composition, the variation of body weight, and the weight of the skeletal muscle, adipose tissues, and liver; as well as fat and protein content in the carcass; and also plasma leptin, ACTH, glucose, insulin and glutamine concentration. We also examined through flow cytometry CD3 and CD4, as well as the celularity in the thymus. The maximum consumption of oxygen and the performance were also assessed. The results demonstrate that endurance training in rats submitted to the chronic malnutrition protocol promoted reduction of body weight and of corporal adiposity; an increase in the relative contribution of muscle to body weight; the reestablishment of glicemia; improval of insulin/glucose reason, suggesting increased sensitivy to insulin; an increase of muscle glycogen content; enhanced oxygen consumption; are recovery of the morphology and physiology of the thymus, together with a proliferative response of the spleen and lymph nodes stimulated with IL2. We conclude in such a way that moderate intensity training restored thymus morphology and the capacity of maturation of CD3 and CD4 and also timocyte number and the of proliferative response to IL2 stimulation.

Chez les vertébrés gnathostomes, le système immunitaire repose en grande partie sur les lymphocytes T qui se développent dans un organe conservé évolutivement : le thymus. Chez les mammifères, cet organe constitue une cible privilégiée pour les œstrogènes. La question soulevée ici est donc de savoir si c’est également le cas chez les poissons téléostéens. Dans ce but, la distribution des différents sous-types de récepteurs aux œstrogènes a d’abord été étudiée dans le contexte d’une description de l’anatomie fonctionnelle du microenvironnement thymique. Par la suite, l’expression de gènes relatifs à la fonction thymique et aux différents sous-types de lymphocyte T a été analysée dans le thymus, le rein-antérieur et la rate de bars exposés au 17ß-œstradiol. De plus, la capacité de flambée oxydative a été évaluée sur des leucocytes du rein-antérieur et de rate à la suite d’expositions in vivo et in vitro. Finalement, la variation du nombre de thymocytes a été examinée sur des bars capturés durant trois ans. La thèse fournit de nouvelles connaissances concernant l’évolution des fonctions immunomodulatrices des œstrogènes sur la différenciation des cellules T. En effet, en plus d’une organisation morpho-fonctionnelle fortement conservée, la distribution des sous-types de récepteurs aux œstrogènes ainsi que les effets œstrogéniques apparaissent conservés au cours de l’évolution. Nos résultats suggèrent que, chez le bar comme chez les mammifères, les œstrogènes (1) stimulent une voie alternative de maturation des lymphocytes T ayant des propriétés similaires aux cellules immunitaires innées, (2) augmentent la tolérance immunitaire et (3) régulent la plasticité du thymus. / Jawed vertebrates have developed an efficient adaptive immune system partly based on T lymphocytes. They develop in an evolutionarily conserved organ, the thymus. In mammals, endogenous oestrogens are well known to regulate thymus function and plasticity. The question is, therefore, whether this is also the case in lower vertebrates, such as teleosts. To achieve these aims, firstly the distribution of oestrogen receptor subtypes was investigated on the background of a detailed description of the functional anatomy of the thymic microenvironment. Secondly, thymic function- and T cell-related gene expression was analysed in the thymus, the head-kidney and the spleen of sea bass exposed to 17ß-oestradiol. Moreover, the oxidative burst capacity in the two latter organs was evaluated in vivo and in vitro in leucocytes of the head-kidney and spleen following exposure to oestrogen. Eventually, age- and size-dependent variations in thymocyte number were examined in sea bass caught at various time points over three years. The thesis provides new insights into the evolution of the immunomodulatory function of oestrogen with respect to the thymic and peripheral T cell differentiation in vertebrates. As a matter of fact, in addition to a highly conserved morpho-functional organisation, the distribution of oestrogen receptor subtypes as well as the oestrogenic effects appear to be evolutionarily conserved. Our results suggest that in sea bass, similar to mammals, oestrogen (1) stimulates a thymic alternative pathway of T cell maturation with innate-like properties, (2) enhances immune tolerance by promoting Treg differentiation, and (3) actively regulate thymic plasticity.

Introdução: o timo é importante órgão linfoide do sistema imunológico. Estudos mostraram que, durante o período fetal, a atrofia desse órgão faz parte da resposta adaptativa do feto ao ambiente intrauterino adverso, como a desnutrição crônica causada pela insuficiência placentária. Essa situação pode explicar a associação entre restrição de crescimento intrauterino e as alterações no sistema imunológico após o nascimento, na infância e na adolescência. Objetivos: analisar as dimensões do timo fetal pela ultrassonografia em gestações com insuficiência placentária, comparando com gestações de alto risco sem insuficiência placentária e gestações de baixo risco. Métodos: estudo prospectivo com 30 gestações com insuficiência placentária (Doppler de artéria umbilical com índice de pulsatilidade > p95) comparadas com 30 de alto risco e 30 de baixo risco (grupo controle). Os critérios de inclusão foram: idade gestacional entre 26 e 37 semanas, feto único e vivo, ausência de malformações fetais, membranas íntegras, ausência de sinais de trabalho de parto, ausência de infecção materna ou fetal e não realização de corticoterapia antes da avaliação ultrassonográfica fetal. O timo fetal foi identificado na interface com os pulmões, na altura dos três vasos da base do coração, no corte do tórax fetal. Foram realizadas três medidas do diâmetro transverso (DT) e do perímetro (P) do timo, e as médias foram utilizadas para análise, transformadas em escores zeta, de acordo com a idade gestacional em que se efetuou a medida. Foram realizadas as medidas ultrassonográficas da circunferência cefálica (CC) e do comprimento do fêmur (CF) fetal, com as quais se calculou as relações DT/CF, DT/CC, P/CF e P/CC. Resultados: o grupo com insuficiência placentária apresentou mediana significativamente maior do escore zeta do IP da artéria umbilical quando comparado ao grupo de alto risco e controle (4,6 vs. -0,5 vs. -0,2, p < 0,001). As medidas do timo fetal no grupo com insuficiência placentária [escore zeta do DT (média=-0,69; DP=0,83) e escore zeta do P (média=-0,73; DP=0,68)] foram significativamente (p < 0,001) menores quando comparadas aos grupos de alto risco [escore zeta do DT (média=0,49; DP=1,13) e escore zeta do P (média=0,45; DP=0,96)] e controle [escore zeta do DT (média=0,83; DP=0,85) e escore zeta do P (média=0,26; DP=0,89)]. Nas relações estudadas, houve diferença significativa (p < 0,05) na média dos grupos: insuficiência placentária (DT/CC=0,10, P/CF=1,32 e P/CC=0,26); alto risco (DT/CC=0,11, P/CF=1,40 e P/CC=0,30) e controle (DT/CC=0,11, P/CF=1,45 e P/CC=0,31). Conclusão: em gestações complicadas pela insuficiência placentária, ocorre redução das dimensões do timo fetal sugerindo que pode ser decorrente da adaptação fetal ao ambiente intrauterino adverso / Introduction: thymus gland is an important lymphoid organ involved in immune response. Studies have shown that during fetal life, thymus atrophy is part of an adaptive response to a compromised intrauterine environment, like chronic malnutrition due to placental insufficiency. This may explain the association between intrauterine growth restriction and later altered immune function. Objective: to evaluate fetal thymus by ultrasonography in pregnancies with placental insufficiency and compare to high risk pregnancies without placental insufficiency and low risk pregnancies. Methods: a prospective study with 30 pregnancies with placental insufficiency (umbilical artery Doppler with pulsatility index > p95), compared to 30 high risk pregnancies and 30 low risk pregnancies (control group). The inclusion criteria were: gestational age ranging from 26 to 37 weeks, singleton pregnancies, absence of fetal malformations, intact membranes, not in labor, no signs of maternal or fetal infection, and no corticotherapy before the ultrasound evaluation. Fetal thymus was identified in its interface with the lungs, at the level of the tree-vessel view of the fetal thorax. Three measures of thymus transverse diameter (TD) and perimeter (P) were made, and the media were converted into zeta score according to the gestational age. Head circumference (HC) and femur length (F) were also measured and used in the calculation of the relations TD/F, TD/HC, P/F, P/HC. Results: the group with placental insufficiency presented median of umbilical artery PI elevated, when compared to high risk pregnancies and low risk pregnancies (4.6 vs. -0.5 vs. -0.2, p < 0.001). Fetal thymus measurements were significantly (p < 0.001) lower in pregnancies with placental insufficiency [TD zeta score (media=-0.69; SD=0.83) and P zeta score (media=-0.73; SD=0.68)] when compared to high risk pregnancies [TD zeta score (media=0.49; SD=1.13) and P zeta score (media=0.45; DP=0.96)] and control group [TD zeta score (media=0.83; SD=0.85) and P zeta score (media=0.26; SD=0.89)]. There was significant difference (p < 0,05) in the relations studied among the groups: pregnancies with placental insufficiency (TD/HC=0.10, P/F=1.32 e P/HC=0.26), high risk pregnancies (TD/HC=0.11, P/F=1.40, P/HC=0.30) and control group (DT/HC=0.11, P/F=1.45, P/HC=0.31). Conclusion: fetal thymus measurements are reduced in pregnancies with placental insufficiency, suggesting that it is a fetal adaptive response for adverse environment

O timo é o órgão linfóide primário responsável pela maturação dos linfócitos T onde se observam estruturas e células especializadas. A sinalização intra-tímica durante a maturação de linfócitos T não é bem esclarecida. Entre outras, a via de sinalização Notch, composta por receptores (Notch 1 a 4) e ligantes (DLL1, 3 e 4, Jagged 1 e 2), pode regular este processo. Neste trabalho temos como objetivo avaliar a expressão gênica e proteica de receptores e ligantes Notch nas diferentes fases de maturação de linfócitos T, linfócitos T reguladores naturais (nTreg) e células dendriticas tímicas (tDC). Para tanto, timos de 10 crianças submetidas à cirurgia cardíaca corretiva foram manipulados e as populações CD4-CD8-, CD4+CD8+, CD4+CD8-, CD4-CD8+, nTreg e tDC foram purificadas por citometria de fluxo. O RNA total foi isolado e os genes NOTCH1, 2 e 3, DLL1 e 4, JAG1 e 2, FOXP3 foram amplificados por RT-PCR. Alguns fragmentos de tecido foram avaliados por imunohistoquímica, quanto a expressão dos receptres Notch 1, 2, 3 e 4 e dos ligantes, DLL1 e 4, Jagged 1 e 2 em timócitos totais, células FOXP3+ e células S100+ em cada região tímica. Todos os genes de receptores e ligantes Notch foram expressos nas populações estudadas. Na população CD4-CD8- o gene NOTCH1 é mais expresso em comparação as outras populações de timócitos imaturos. Na população CD4+CD8+ o gene NOTCH2 é menos expresso, e o gene JAG2 mais expresso quando comparados à população CD4+CD8-. Os demais genes de receptores ligantes Notch são expressos de maneira similar entre as populações de timócitos. A avaliação relativa dos genes Notch nas populações de timócitos mostrou uma maior expressão do gene DLL1 na população CD4+CD8- e JAG1 na população CD4-CD8+ em comparação à CD4-CD8-. A expressão dos receptores e ligantes Notch no tecido mostrou ser homogênea entre as regiões. As nTreg expressam o gene do ligante JAG1 em maior nível entre os avaliados. A expressão gênica relativa das nTreg mostrou uma maior expressão de NOTCH1, NOTCH2, DLL4 e JAG1 e menor expressão de NOTCH3, DLL1 e JAG2 em relação as CD4-CD8-. Quando a relação utilizou a população CD4+CD8- observamos que as nTreg expressam mais os genes NOCTH1, NOCTH2, NOTCH3, DLL4 e JAG1, e em níveis similares DLL1 e JAG2. A avaliação histológica mostrou uma maior expressão de DLL4 em nTreg em comparação às demais proteínas avaliadas, e uma distribuição homogênea entre as regiões com exceção de Notch3 e Jagged2. As tDC mostraram uma maior expressão do gene JAG1 em comparação aos demais, e uma maior expressão da proteína DLL4. A expressão do receptor Notch2 em tDC difere entre as regiões tímicas. Em conjunto, nossos resultados mostraram que os receptores e ligantes Notch são expressos de forma gênica e proteica em todos os estágios de maturação de linfócitos T, nTreg e tDC do timo humano, com algumas variações quanto ao nível de expressão e distribuição no timo. Dados que se assemelham às avaliações murinas, porém com pontos a serem discutidos. Nossa inédita avaliação em nTreg propõem uma nova abordagem ao envolvimento da via Notch em sua maturação e a avaliação das tDCs sugere sua participação direta via Notch na maturação dos timócitos humanos / The thymus is a primary lymphoid organ responsible of maturing T lymphocytes, where specialized structures and cells are observed. The intrathymic signaling during lymphocytes maturation is unclear. Among them, Notch signaling pathway, which comprises in receptors (Notch1-4) and ligands (DLL1, 2 and 3, Jaaged1 and 2), may regulate this process. In this work our aim is to evaluate the expression of Notch receptors and ligands in different phases of T lymphocytes maturation, natural T regulatory cells (nTreg), and thymic dendritic cells (tDC). For this purpose, thymuses from 10 children who underwent corrective cardiac surgery were manipulated and populations CD4-CD8-, CD4+CD8+, CD4+CD8-, CD4- CD8+, nTreg and tDC were sorted by flow cytometry. Total RNA was purified and genes NOTCH1, 2 and 3, DLL1 and 4, JAG1 and 2, FOXP3 were amplified by RT-PCR. Some thymic fragments were evaluated by immunohistochemistry and screened for expression of Notch 1, 2, 3 and 4 receptors, DLL1 and 4, Jagged and e 2 ligands in total thymocytes, FOXP3+ cells and S100+ cells in each thymic region. All Notch receptors and ligands genes were expressed in studied populations. In CD4-CD8- subset NOTCH1 gene is more expressed in comparison to others immature thymocytes. In CD4+CD8+ subset NOTCH2 gene is less expressed, and JAG2 gene is more expressed when compared to CD4+CD8- population. The other receptors and ligands genes were expressed in a similar level among developing lymphocytes subsets. The relative Notch genes evaluation in developing lymphocytes populations showed a higher expression of DLL1 gene in CD4+CD8- population and JAG1 gene in CD4-CD8+ subset in comparison to CD4-CD8- thymocytes. The Notch receptors and ligands expression in thymic tissue showed to be homogeneous between thymic regions. The nTreg cells express JAG1 ligand gene in highest level among evaluated genes. The relative gene expression in nTreg presented higher expression of NOCTH1, NOTCH2, DLL4 and JAG1 genes, and low levels of NOTCH3, DLL1 and JAG2 related to CD4-CD8- subset. When relative gene expression were performed using CD4+CD8- subset, we observed that nTreg cells expressed more NOCTH1, NOCTH2, NOTCH3, DLL4 and JAG1, and in a similar level of expression DLL1 and JAG2 genes. The histological analysis showed that DLL4 was more expressed in nTreg cells in comparison to others proteins evaluated in this work, and a homogeneous distribution in thymic regions, in exception Notch3 and Jagged2. tDC cells presented higher expression of JAG1 gene among the others, and a higher expression of DLL4 protein. Notch2 expression in tDC was different between thymic regions. All together, our results showed that both genes and proteins of Notch receptors and ligands are expressed in distinct developmental stages of the maturation of T lymphocytes and nTreg cells and in the tDC cells in human thymus, with some variations in levels of expression and distribution in the thymus. These data are similar to the murine evaluations, but with some issues to be discussed. Our unpublished assessment in nTreg propose a new approach about the involvement of Notch pathway in its maturation and the evaluation of tDC suggests its direct participation of Notch signaling in the process of human thymocytes maturation

Há dados na literatura indicando que as células que saem do timo com o fenótipo CD4+CD25+ são desenvolvidas continuamente como uma linhagem independente e possuem um papel importante no processo de regulação da resposta imune. Essas células são chamadas células T reguladoras naturais. Várias questões sobre estas células permanecem em aberto, como por exemplo, como elas são geradas, o que é determinante na sua atividade reguladora e que marcadores específicos podem ser usados para identificá-las? Dentro deste contexto, o nosso objetivo neste trabalho foi identificar no timo e em timócitos CD4+/CD25+ humanos, novas moléculas potencialmente importantes no desenvolvimento e/ou na atividade supressora das células T reguladoras naturais. Para este objetivo, utilizamos a abordagem de phage display, com uma biblioteca de fagos de peptídeos, e timos humanos obtidos de pacientes portadores de cardiopatias congênitas, submetidos a cirurgias cardíacas realizadas no InCor. A busca dessas moléculas foi feita, separadamente, em 3 tipos de material biológico: timócitos totais, fragmento do tecido tímico e timócitos CD4+/CD25+. Antes da incubação da biblioteca de fagos com os timócitos totais e timócitos CD4+/CD25+ (separação em FACS), foi realizada uma etapa de preclearing, incubando-se a biblioteca de fagos com um pool de células mononucleares de sangue periférico (PBMC) ou timócitos CD4+/CD25-, respectivamente. Os fagos não ligantes, recuperados desta etapa, foram então incubados com as células de interesse. Para o tecido tímico não foi feita etapa de pre-clearing. Os fagos obtidos com os diferentes materiais biológicos foram recuperados em cultura de bactérias e usados em ciclos posteriores de seleção. Após três ciclos de seleção, os fagos foram seqüenciados e identificados quanto à expressão de peptídeos ligantes para timócitos totais, timo e timócitos CD4+/CD25+, e analisados em bancos de dados no BLAST. Os fagos selecionados para validação um ligante de tecido tímico: M2C e um ligante de timócitos CD4+/CD25+: R2A fazem similaridade a duas proteínas associadas ao metabolismo da Vitamina D3, molécula envolvida em imunorregulação e indução de tolerância, em diversos modelos experimentais. Porém, não há dados na literatura a respeito do seu papel em células T reg naturais. Na validação molecular desses fagos, apesar de certa variabilidade entre os diferentes ensaios, verificamos, por ELISA, que os fagos se ligam preferencialmente a 1,25 diidroxivitamina D3, forma ativa da Vitamina D3. Entretanto, nos ensaios de validação funcional, a influência da vitamina D na diferenciação dessas células não foi confirmada de forma consistente, uma vez que só tivemos aumento no número de células CD4+/CD25+, em cultura com Vitamina D, em poucos experimentos. As moléculas identificadas no presente estudo podem ter implicações relevantes no processo de diferenciação e na atividade de células T CD4+CD25+ reguladoras e serão mais investigadas na continuidade deste trabalho. / There are consistent data in literature indicating that thymic CD4+CD25+ cells play an important role in immune regulation and are continuously developed as an independent lineage in the thymus. These cells are known as natural regulatory T cells. Several questions about these cells remain unanswered, such as how they are generated, what is determinant in their regulatory function and which specific molecular markers can be used to identify them. Taking this into consideration, our aim was to identify new potentially important molecules in the development and/or supressive function of natural regulatory T cells, both in the thymus and in CD4+CD25+ thymocytes. For this, the phage display technique was employed, with a peptide phage library and thymic specimens obtained from children who underwent corrective cardiac surgery at the Heart Institute (InCor), in São Paulo. The search for these molecules was separately performed in 3 types of biological material: thymic tissue, thymocytes and CD4+CD25+ thymic cells. In the first stage, the phage peptide-library was incubated with a pool of PBMC (peripheral blood mononuclear cells). After the incubation, phages bound to PBMC were discarded (pre-clearing). In the second stage, unbound phages were incubated with either total thymocytes or CD4+CD25+ thymic cells. The pre-clearing stage was not perfomed in the thymic tissue. The phages obtained with after incubation with the different biological materials were recovered in E. coli culture and used in additional cycles of selection. After three rounds of selection, the recovered phages from the total thymocytes, from thymic tissue and thymocytes CD4+CD25+ were sequenced and their ligands identified. Among the phages selected for validation one ligand of thymic tissue: M2C and one ligand of CD4+CD25+ thymocytes: R2A present similarity to two proteins associated to the metabolism of Vitamin D3, a molecule involved in imunoregulation and toelrance induction in several experimental models. However, there are no data in the literature concerning the possible role of this moelcule in natural regulatory T cells. In the molecular validation of theses phages, although some variability between the diffeterent assays we have verified by ELISA, that the phages present preferential binding to the 1,25 dhydroxyvitamin D3, the active form of Vitamin D3. However, in the functional validation assays, the influence of the Vitamin D3 in the differentiation of these cells could not be consistently confirmed since we could observe an increase in the number of CD4+CD25+ cells cultured with vitamin D in only a few experiments. The ligand-receptor molecules we have defined in this study may have relevant implications in the development of CD4+CD25+ regulatory T cells in the thymus

O timo é o órgão linfóide primário responsável pela maturação dos linfócitos T onde se observam estruturas e células especializadas. A sinalização intra-tímica durante a maturação de linfócitos T não é bem esclarecida. Entre outras, a via de sinalização Notch, composta por receptores (Notch 1 a 4) e ligantes (DLL1, 3 e 4, Jagged 1 e 2), pode regular este processo. Neste trabalho temos como objetivo avaliar a expressão gênica e proteica de receptores e ligantes Notch nas diferentes fases de maturação de linfócitos T, linfócitos T reguladores naturais (nTreg) e células dendriticas tímicas (tDC). Para tanto, timos de 10 crianças submetidas à cirurgia cardíaca corretiva foram manipulados e as populações CD4-CD8-, CD4+CD8+, CD4+CD8-, CD4-CD8+, nTreg e tDC foram purificadas por citometria de fluxo. O RNA total foi isolado e os genes NOTCH1, 2 e 3, DLL1 e 4, JAG1 e 2, FOXP3 foram amplificados por RT-PCR. Alguns fragmentos de tecido foram avaliados por imunohistoquímica, quanto a expressão dos receptres Notch 1, 2, 3 e 4 e dos ligantes, DLL1 e 4, Jagged 1 e 2 em timócitos totais, células FOXP3+ e células S100+ em cada região tímica. Todos os genes de receptores e ligantes Notch foram expressos nas populações estudadas. Na população CD4-CD8- o gene NOTCH1 é mais expresso em comparação as outras populações de timócitos imaturos. Na população CD4+CD8+ o gene NOTCH2 é menos expresso, e o gene JAG2 mais expresso quando comparados à população CD4+CD8-. Os demais genes de receptores ligantes Notch são expressos de maneira similar entre as populações de timócitos. A avaliação relativa dos genes Notch nas populações de timócitos mostrou uma maior expressão do gene DLL1 na população CD4+CD8- e JAG1 na população CD4-CD8+ em comparação à CD4-CD8-. A expressão dos receptores e ligantes Notch no tecido mostrou ser homogênea entre as regiões. As nTreg expressam o gene do ligante JAG1 em maior nível entre os avaliados. A expressão gênica relativa das nTreg mostrou uma maior expressão de NOTCH1, NOTCH2, DLL4 e JAG1 e menor expressão de NOTCH3, DLL1 e JAG2 em relação as CD4-CD8-. Quando a relação utilizou a população CD4+CD8- observamos que as nTreg expressam mais os genes NOCTH1, NOCTH2, NOTCH3, DLL4 e JAG1, e em níveis similares DLL1 e JAG2. A avaliação histológica mostrou uma maior expressão de DLL4 em nTreg em comparação às demais proteínas avaliadas, e uma distribuição homogênea entre as regiões com exceção de Notch3 e Jagged2. As tDC mostraram uma maior expressão do gene JAG1 em comparação aos demais, e uma maior expressão da proteína DLL4. A expressão do receptor Notch2 em tDC difere entre as regiões tímicas. Em conjunto, nossos resultados mostraram que os receptores e ligantes Notch são expressos de forma gênica e proteica em todos os estágios de maturação de linfócitos T, nTreg e tDC do timo humano, com algumas variações quanto ao nível de expressão e distribuição no timo. Dados que se assemelham às avaliações murinas, porém com pontos a serem discutidos. Nossa inédita avaliação em nTreg propõem uma nova abordagem ao envolvimento da via Notch em sua maturação e a avaliação das tDCs sugere sua participação direta via Notch na maturação dos timócitos humanos / The thymus is a primary lymphoid organ responsible of maturing T lymphocytes, where specialized structures and cells are observed. The intrathymic signaling during lymphocytes maturation is unclear. Among them, Notch signaling pathway, which comprises in receptors (Notch1-4) and ligands (DLL1, 2 and 3, Jaaged1 and 2), may regulate this process. In this work our aim is to evaluate the expression of Notch receptors and ligands in different phases of T lymphocytes maturation, natural T regulatory cells (nTreg), and thymic dendritic cells (tDC). For this purpose, thymuses from 10 children who underwent corrective cardiac surgery were manipulated and populations CD4-CD8-, CD4+CD8+, CD4+CD8-, CD4- CD8+, nTreg and tDC were sorted by flow cytometry. Total RNA was purified and genes NOTCH1, 2 and 3, DLL1 and 4, JAG1 and 2, FOXP3 were amplified by RT-PCR. Some thymic fragments were evaluated by immunohistochemistry and screened for expression of Notch 1, 2, 3 and 4 receptors, DLL1 and 4, Jagged and e 2 ligands in total thymocytes, FOXP3+ cells and S100+ cells in each thymic region. All Notch receptors and ligands genes were expressed in studied populations. In CD4-CD8- subset NOTCH1 gene is more expressed in comparison to others immature thymocytes. In CD4+CD8+ subset NOTCH2 gene is less expressed, and JAG2 gene is more expressed when compared to CD4+CD8- population. The other receptors and ligands genes were expressed in a similar level among developing lymphocytes subsets. The relative Notch genes evaluation in developing lymphocytes populations showed a higher expression of DLL1 gene in CD4+CD8- population and JAG1 gene in CD4-CD8+ subset in comparison to CD4-CD8- thymocytes. The Notch receptors and ligands expression in thymic tissue showed to be homogeneous between thymic regions. The nTreg cells express JAG1 ligand gene in highest level among evaluated genes. The relative gene expression in nTreg presented higher expression of NOCTH1, NOTCH2, DLL4 and JAG1 genes, and low levels of NOTCH3, DLL1 and JAG2 related to CD4-CD8- subset. When relative gene expression were performed using CD4+CD8- subset, we observed that nTreg cells expressed more NOCTH1, NOCTH2, NOTCH3, DLL4 and JAG1, and in a similar level of expression DLL1 and JAG2 genes. The histological analysis showed that DLL4 was more expressed in nTreg cells in comparison to others proteins evaluated in this work, and a homogeneous distribution in thymic regions, in exception Notch3 and Jagged2. tDC cells presented higher expression of JAG1 gene among the others, and a higher expression of DLL4 protein. Notch2 expression in tDC was different between thymic regions. All together, our results showed that both genes and proteins of Notch receptors and ligands are expressed in distinct developmental stages of the maturation of T lymphocytes and nTreg cells and in the tDC cells in human thymus, with some variations in levels of expression and distribution in the thymus. These data are similar to the murine evaluations, but with some issues to be discussed. Our unpublished assessment in nTreg propose a new approach about the involvement of Notch pathway in its maturation and the evaluation of tDC suggests its direct participation of Notch signaling in the process of human thymocytes maturation

3BP2 is a pleckstrin homology (PH) domain- and Src homology 2 (SH2) domain-containing adapter protein that has been linked through genetic evidence to a rare human disease called cherubism 146. 3BP2 was originally cloned in a screen to identify c-Abl SH3 binding proteins 23,24. In overexpression studies, 3BP2 has been implicated as a positive regulatory adapter molecule coupled to immunoreceptor on T cells 67,69,70, B cells 68, NK cells 71-73 and mast cells 74,75. It was also evident that 3BP2 forms complexes with a number of signaling molecules, such as Zap-70, LAT, phospholipase C-γ1 (PLC-γ1), Grb2, Cbl, and Fyn in Jurkat cells 67 and Vav1, Vav2, PLC-γ, and Syk in Daudi B cells 68. Despite the growing body of biochemical data to support the importance of 3BP2 in cells of the hematopoietic lineage, a clear picture of the biological function of 3BP2 has yet to emerge. To elucidate the in vivo function of 3BP2, our laboratory has generated 3BP2 gene-deficient mice through homologous recombination 452. The 3BP2-deficient (3BP2-/-) mice were born at the expected Mendelian frequency and were fertile and viable. 3BP2-/- mice accumulate splenic marginal-zone (MZ) B cells, possess a reduced frequency of peritoneal B-1 B cells, and have a diminished thymus-independent type 2 (TI-2) antigen response. 3BP2-/- B cells demonstrate diminished proliferation and cell survival following cross-linking of the B-cell receptor (BCR). Following BCR ligation, 3BP2 might be recruited to BCR complex through its inducible interaction with BCR costimulatory molecule CD19. In the absence of 3BP2, the activation of BCR downstream effectors such as MAPK Erk1/2, JNK, and c-Abl is normal; however, 3BP2 deficiency leads to defects in Syk phosphorylation and calcium flux. In addition to defects in peripheral B cell activities, 3BP2 deficiency contributes to defects in neutrophil activities. In response to the chemotactic peptide, fMLF, 3BP2-/- neutrophils fail to establish directional migration in vitro. There is a defect in the accumulation of filamentous actin at the leading edge of migrating 3BP2-/- neutrophils which might be responsible for the random movement of these cells under shallow gradient of fMLF. In vivo, there is a delay in the recruitment of circulating neutrophils to the site of chemically induced inflammation in 3BP2-/- mice. Compared to wildtype neutrophils, 3BP2-/- neutrophils fail to properly produce superoxide anion (O2-) following fMLF stimulation. Defects in both directional migration and superoxide production of 3BP2-/- neutrophils might contribute to the reduction in bacteria clearance and the increased mortality in 3BP2-/- mice post Listeria Monocytogenes infection. In Chapter 1 of this thesis, I have reviewed basic structures and functions of the domain modules found in adapter proteins. In addition, I have reviewed the findings from numerous reports on the function of 3BP2 in different cell types. A discussion of the physical appearance and some of the initial characterization of 3BP2-deficient mice (3BP2-/-) we have generated in our laboratory are included in Chapter 1. The second part of Chapter 1 consists of an introduction on B cell receptor signaling pathway and B-cell development and activation. A discussion of G protein-coupled receptor-mediated neutrophil functions can also be found in Chapter 1. Chapter 2 contains all the methods and materials used in my study. Chapter 3 includes the characterization of peripheral B cell compartment of 3BP2-/- mice as well as the role of 3BP2 downstream of B-cell antigen receptor and in T-independent immune response. In chapter 4, I present data from experiments designed to examine the role of 3BP2 downstream of a G protein-coupled receptor, fMLF receptor, of neutrophils. I also show the requirement of 3BP2 in the clearance of Listeria Monocytogenes. In chapter 5, I propose two models for 3BP2 action based on the findings in B cells and neutrophils and discuss future areas for investigation.

3BP2 is a pleckstrin homology (PH) domain- and Src homology 2 (SH2) domain-containing adapter protein that has been linked through genetic evidence to a rare human disease called cherubism 146. 3BP2 was originally cloned in a screen to identify c-Abl SH3 binding proteins 23,24. In overexpression studies, 3BP2 has been implicated as a positive regulatory adapter molecule coupled to immunoreceptor on T cells 67,69,70, B cells 68, NK cells 71-73 and mast cells 74,75. It was also evident that 3BP2 forms complexes with a number of signaling molecules, such as Zap-70, LAT, phospholipase C-γ1 (PLC-γ1), Grb2, Cbl, and Fyn in Jurkat cells 67 and Vav1, Vav2, PLC-γ, and Syk in Daudi B cells 68. Despite the growing body of biochemical data to support the importance of 3BP2 in cells of the hematopoietic lineage, a clear picture of the biological function of 3BP2 has yet to emerge. To elucidate the in vivo function of 3BP2, our laboratory has generated 3BP2 gene-deficient mice through homologous recombination 452. The 3BP2-deficient (3BP2-/-) mice were born at the expected Mendelian frequency and were fertile and viable. 3BP2-/- mice accumulate splenic marginal-zone (MZ) B cells, possess a reduced frequency of peritoneal B-1 B cells, and have a diminished thymus-independent type 2 (TI-2) antigen response. 3BP2-/- B cells demonstrate diminished proliferation and cell survival following cross-linking of the B-cell receptor (BCR). Following BCR ligation, 3BP2 might be recruited to BCR complex through its inducible interaction with BCR costimulatory molecule CD19. In the absence of 3BP2, the activation of BCR downstream effectors such as MAPK Erk1/2, JNK, and c-Abl is normal; however, 3BP2 deficiency leads to defects in Syk phosphorylation and calcium flux. In addition to defects in peripheral B cell activities, 3BP2 deficiency contributes to defects in neutrophil activities. In response to the chemotactic peptide, fMLF, 3BP2-/- neutrophils fail to establish directional migration in vitro. There is a defect in the accumulation of filamentous actin at the leading edge of migrating 3BP2-/- neutrophils which might be responsible for the random movement of these cells under shallow gradient of fMLF. In vivo, there is a delay in the recruitment of circulating neutrophils to the site of chemically induced inflammation in 3BP2-/- mice. Compared to wildtype neutrophils, 3BP2-/- neutrophils fail to properly produce superoxide anion (O2-) following fMLF stimulation. Defects in both directional migration and superoxide production of 3BP2-/- neutrophils might contribute to the reduction in bacteria clearance and the increased mortality in 3BP2-/- mice post Listeria Monocytogenes infection. In Chapter 1 of this thesis, I have reviewed basic structures and functions of the domain modules found in adapter proteins. In addition, I have reviewed the findings from numerous reports on the function of 3BP2 in different cell types. A discussion of the physical appearance and some of the initial characterization of 3BP2-deficient mice (3BP2-/-) we have generated in our laboratory are included in Chapter 1. The second part of Chapter 1 consists of an introduction on B cell receptor signaling pathway and B-cell development and activation. A discussion of G protein-coupled receptor-mediated neutrophil functions can also be found in Chapter 1. Chapter 2 contains all the methods and materials used in my study. Chapter 3 includes the characterization of peripheral B cell compartment of 3BP2-/- mice as well as the role of 3BP2 downstream of B-cell antigen receptor and in T-independent immune response. In chapter 4, I present data from experiments designed to examine the role of 3BP2 downstream of a G protein-coupled receptor, fMLF receptor, of neutrophils. I also show the requirement of 3BP2 in the clearance of Listeria Monocytogenes. In chapter 5, I propose two models for 3BP2 action based on the findings in B cells and neutrophils and discuss future areas for investigation.