Um Projeto Temático de Pesquisa foi desenvolvido no Laboratório de Poluição Ambiental do Departamento de Patologia da Faculdade de Medicina da Universidade de São Paulo com o objetivo de avaliar os efeitos da exposição aguda/crônica ao ar ambiente de um grande centro urbano sobre a saúde. Dentro deste projeto, uma linha de pesquisa foi dedicada ao estudo dos efeitos dessa exposição sobre a saúde reprodutiva feminina. Evidências de estudos epidemiológicos e experimentais implicam os fatores ambientais na infertilidade humana e resultado obstétrico adverso. Contudo, poucos estudos foram conduzidos até o presente para avaliar um possível efeito da exposição à poluição ambiental particulada sobre a saúde reprodutiva feminina. Portanto, o objetivo dos projetos da minha linha de pesquisa é fornecer dados que possam demonstrar os possíveis efeitos da exposição crônica à poluição ambiental particulada sobre a função ovariana e o desenvolvimento embrionário inicial. O objetivo do primeiro projeto desta tese foi avaliar diferentes metodologias utilizadas para a coloração diferencial das linhagens celulares do blastocisto, um método mais adequado para a avaliação de sua qualidade e normalidade. As células de blastocistos intactos de camundongo obtidos através de fertilização in vitro (FIV) foram permeabilizadas e coradas utilizando-se diferentes concentrações de um detergente (TX-100; 0,5% ou 1%) e de iodeto de propídeo (IP; 50 g/mL ou 100 g/mL) e depois disso, incubadas durante a noite em uma solução contendo diferentes fixadores (etanol, metanol, paraformaldeído PFA1% ou 4%) e bisbenzimida. Para a avaliação da qualidade de coloração e contagem diferencial dos núcleos, os blastocistos foram montados em lâminas de vidro e analisados em um microscópio de epifluorescência. O escore de qualidade de coloração foi significativamente diferente (p<0,05) entre todas as soluções fixadoras, sendo maior para o etanol, seguido pelo metanol, PFA1% e PFA4%. Mudanças da concentração do IP e o uso de diferentes soluções de fixação revelaram efeitos significativos na contagem de células da massa celular interna (MCI) e na razão MCI/trofectoderma (TE). Concentrações diferentes do detergente utilizado para a permeabilização celular apresentaram efeitos significativos sobre a contagem de células TE e razão MCI/TE. Concluímos que o protocolo que utiliza TX-100 1% para a permeabilização celular, 50 g/mL de IP para coloração das células TE e etanol como solução de fixação representa o método mais eficiente para a coloração diferencial e contagem das células das linhagens celulares do embrião no estágio de blastocisto. No segundo projeto que compõe esta, o objetivo foi avaliar os efeitos da exposição pré e/ou pós-natal ao ar ambiente sobre a fertilização, desenvolvimento embrionário e segregação das linhagens celulares em blastocistos pré-implantacionais, utilizando o modelo de FIV de camundongo. Fêmeas de camundongo com idade de seis semanas tiveram a ovulação estimulada e foram expostas no período pré- e/ou pós-natal ao ar filtrado (AF-AF), ar filtrado ar ambiente (AF-AA) ou ar ambiente ar ambiente (AA-AA) em câmaras de exposição 24 horas por dia, sete dias na semana, durante nove semanas. Os pontos de avaliação reprodutivos analisados incluíram a duração da gestação, tamanho e peso da prole, índice de nascidos vivos, razão sexual, resposta ovariana à estimulação, taxa de fertilização, desenvolvimento embrionário, taxas de formação e de eclosão dos blastocistos, contagem celular total e proporção da alocação celular à MCI e TE. A duração da gestação, tamanho e peso da prole, índice de nascidos vivos e razão sexual foram similares nos diferentes grupos de exposição. A resposta ovariana não foi afetada pelo protocolo de exposição. Um efeito multivariável para a exposição pré e/ou pós-natal ao material particulado fino ambiente sobre a FIV, o desenvolvimento embrionário e a coloração diferencial dos blastocistos foi observado. A contagem celular na MCI e a razão MCI/TE dos blastocistos produzidos no protocolo AF-AF foram significativamente maiores do que aquelas em blastocistos produzidos nos protocolos FA-AA e AA-AA. Nenhuma diferença na contagem celular total foi observada. Baseando-se nessas observações, nosso estudo sugere que a exposição ao material particulado fino presente no ar ambiente de um grande centro urbano pode afetar negativamente a saúde reprodutiva feminina através da alteração da especificação das linhagens celulares do embrião no estágio de blastocisto. Finalmente, o propósito do terceiro projeto que compõe esta tese foi de avaliar os efeitos da exposição pré e/ou pósnatal ao ar ambiente no final da vida reprodutiva sobre a fertilização, desenvolvimento embrionário e segregação das linhagens celulares em blastocistos pré-implantacionais, utilizando o modelo de FIV de camundongo. Fêmeas de camundongo com idade de cinco meses tiveram a ovulação estimulada e foram expostas no período pré e/ou pós-natal ao ar filtrado (AF-AF), ar filtrado ar ambiente (AF-AA) ou ar ambiente ar ambiente (AA-AA) em câmaras de exposição 24 horas por dia, sete dias na semana, durante seis meses. Os pontos de avaliação reprodutivos foram os mesmos que aqueles utilizados no segundo projeto. A duração da gestação, tamanho e peso da prole, índice de nascidos vivos e razão sexual foram similares nos diferentes grupos de exposição. A resposta ovariana não foi afetada pelo protocolo de exposição. Um efeito multivariável para a exposição pré e/ou pós-natal ao material particulado fino ambiente sobre coloração diferencial dos blastocistos, mas não sobre a FIV e o desenvolvimento embrionário, foi observado. A contagem celular na MCI e a razão MCI/TE dos blastocistos produzidos no protocolo AF-AF foram significativamente maiores do que aquelas em blastocistos produzidos nos protocolos FA-AA e AA-AA. A contagem celular do TE dos blastocistos produzidos no protocolo FA-FA foi significativamente menor do que aquela em blastocistos produzidos nos protocolos FA-AA e AA-AA. A contagem celular total foi similar entre os grupos. Nosso estudo sugere que a exposição à poluição ambiental particulada de um grande centro urbano não altera a função ovariana, mas pode afetar negativamente a saúde reprodutiva feminina no período final do menacme, através da alteração da especificação das linhagens celulares do embrião no estágio de blastocisto / A thematic research project to evaluate the health effects of acute/chronic exposure to ambient air in a large urban center was developed at the Air Pollution Laboratory in the Department of Pathology at the University of São Paulo School of Medicine. Within this project a specific research line was committed to the study of the effects of this exposure on female reproductive health. Evidence from epidemiological and experimental studies implied environmental factors as possible contributors to human infertility and poor obstetric outcome. However, very few studies evaluating a possible effect of exposure to particulate air pollution on female reproductive health have been conducted so far. Thus, the aim of the projects in my research line was to provide data that could show the possible effects of chronic exposure to particulate air pollution on ovarian function and early embryo development. The objective of the first project was to assess different methodologies used in cell lineage differential staining of the blastocyst, a method for more accurate evaluation of its quality and normality. Cells of zona-intact mouse blastocysts obtained from in vitro fertilization (IVF) were permeabilized and stained using different concentrations of a detergent (TX-100; 0.5% or 1%) and propidium iodide (PI; 50 g/mL or 100 g/mL) followed by overnight incubation in a solution containing different fixatives (ethanol, methanol, paraformaldehyde - PFA 1% or 4%) and bisbenzimide. To evaluate the staining quality and count the nuclei differentially, blastocysts were mounted and viewed using epifluorescence microscopy. Staining quality scores were significantly different (P < 0.05) among all fixative solutions with the highest for ethanol followed by methanol, PFA1%, and PFA4%. Changes in PI concentration and use of different fixative solutions revealed significant effects on inner cell mass (ICM) cell count and ICM/trophectoderm (TE) ratio. Different concentrations of the detergent used for cell permeabilization showed significant effects on TE cell counts and ICM/TE ratio. I concluded that the protocol using 1% TX-100 for cell permeabilization, 50 g/mL of PI for TE cell staining, and ethanol as a fixative solution is the most efficient method for cell lineage differential staining and counting at the blastocyst stage. In the second project the objective was to evaluate the effects of preand/ or postnatal exposure to ambient air on fertilization, embryo development, and cell lineage segregation in preimplantation blastocysts using the IVF mouse model. Six-week old superovulated mice were preand/ or postnatally exposed to filtered air (FA-FA), filtered-ambient air (FAAA), or ambient air (AA-AA) in exposure chambers 24/7 for nine weeks. Reproductive endpoints evaluated included gestation length, litter size, litter birth weight, live birth index, sex ratio, ovarian response to superovulation, fertilization rate, embryo development, blastocyst and hatching rates, total cell count, and proportion of cell allocation to ICM and TE. Gestation length, litter size, litter birth weight, live birth index, and sex ratio were similar among exposure groups. Ovarian response was not affected by the exposure protocol. A multivariate effect for pre- and/or postnatal exposure to ambient fine particulate matter on IVF, embryo development, and blastocyst differential staining was found. Cell counts in ICM and ICM/TE ratios in blastocysts produced in the FA-FA protocol were significantly higher than in blastocysts produced in FA-AA and AA-AA protocols. No difference in the total cell count was observed. Based on these observations the study suggests that exposure to ambient fine particulate matter in a large urban center may negatively affect female reproductive health by disrupting the lineage specification at the blastocyst stage. Finally, the purpose of the third project was to evaluate the effects of pre- and/or postnatal exposure to particulate air pollution on fertilization, embryo development, and cell lineage segregation in preimplantation blastocysts during the late-life reproductive period using the IVF mouse model. Five-month-old superovulated mice were pre- and/or postnatally exposed to filtered air (FA-FA), filtered-ambient air (FA-AA), or ambient air (AA-AA) in exposure chambers 24/7 during six months. Reproductive endpoints were the same as the ones selected for the second project. Gestation length, litter size, litter birth weight, live birth index, and sex ratio were similar among exposure groups. Ovarian response was not affected by the exposure protocol. A multivariate effect for pre- and/or postnatal exposure to ambient air on blastocyst differential staining but not on IVF and embryo development was found. Cell counts in ICM and ICM/TE ratios in blastocysts produced in the FA-FA protocol were significantly higher than in blastocysts produced in FA-AA and AA-AA protocols. Cell counts in TE cells in blastocysts produced in the FA-FA protocol were significantly lower than in blastocysts produced in FA-AA and AA-AA protocols. The total cell count was similar among groups. This study suggests that exposure to particulate air pollution in a large urban center has no effect on ovarian function but may negatively affect female reproductive health in the late-life period by disrupting the lineage specification at the blastocyst stage.

O presente estudo avaliou a influência das concentrações de ácidos graxos não esterificados (AGNE Alto vs. Baixo) no dia 44±3 pós-parto, e dos dias pós-parto nas concentrações de metabólitos (&#496;-hidroxibutirato e glicose) e na qualidade oocitária e produção in vitro de embriões de vacas Holandesas no início da lactação (até 90 dias pós-parto). O experimento foi realizado na Fazenda Santa Rita (Agrindus S/A) localizada no município de Descalvado SP. A partir da data do parto foram selecionadas 30 vacas Holandesas para serem aspiradas a cada 14 dias em cinco diferentes momentos no início da lactação (30±3, 44±3, 58±3, 72±3 e 86±3 dias pós-parto). No momento da aspiração folicular (OPU), foram realizadas as colheitas de sangue para dosagem dos metabólitos, a avaliação do escore de condição corporal (ECC) e a contagem dos folículos visualizados. Os procedimentos de produção in vitro de embriões (maturação, fertilização e cultivo) foram realizados no laboratório da Bioembryo, localizado no município de Bauru - SP. A análise estatística foi realizada pelo procedimento GLM do SAS. Não se observou efeito de tratamento (Alto AGNE = 0,45 vs. Baixo AGNE = 0,52 mmol/L; P=0,20) e de tempo (30±3 = 0,54; 44±3 = 0,43; 58±3 = 0,43; 72±3 = 0,52 e 86±3 = 0,51 mmol/L; P=0,11) para as concentrações de &#946;-hidroxibutirato. Para as concentrações de glicose não se verificou efeito do tratamento (Alto AGNE = 61,1 vs. Baixo AGNE = 63,6 mg/dL; P=0,26). No entanto, observou-se efeito de tempo para as concentrações de glicose (30±3 = 60,1; 44±3 = 63,0; 58±3 = 63,5; 72±3 = 62,1 e 86±3 = 63,0 mg/dL; P=0,03). O tratamento (Alto vs. Baixo AGNE) não influenciou a quantidade de folículos recrutados (P=0,36), oócitos totais recuperados (P=0,28) e oócitos viáveis (P=0,25). Assim como o tempo não alterou a quantidade de folículos recrutados (P=0,87), oócitos totais recuperados (P=0,42) e oócitos viáveis (P=0,44). A quantidade de oócitos grau I não foi influenciada pelo tratamento (Alto vs. Baixo AGNE; P=0,14). Porém, os dias pós-parto reduziram a sua quantidade (P=0,05). A quantidade de oócitos clivados por vaca aspirada (P=0,45) e a taxa de clivagem (P=0,95) não apresentaram diferenças estatísticas conforme as concentrações de AGNE (Alto vs. Baixo) no dia 44 pós-parto. Os dias pós-parto também não alteraram a quantidade de oócitos clivados por vaca aspirada (P=0,31) e a taxa de clivagem (P=0,80). Para a produção in vitro de embriões, a quantidade de blastocisto por vaca aspirada conforme as concentrações de AGNE (Alto = 0,4 vs. Baixo = 1,2; P=0,37) e os dias pós-parto (30±3 = 0,4; 44±3 = 0,7; 58±3 = 0,8; 72±3 = 0,9 e 86±3 = 1,2; P=0,39) não apresentaram diferenças estatísticas. Assim como, a taxa de blastocisto para os animais dos grupos (Alto AGNE = 6,2% vs. Baixo AGNE = 11,6%; P=0,51) e para os diferentes momentos pós-parto (30±3 = 4,8%; 44±3 = 8,9%; 58±3 = 10,7%; 72±3 = 10,0% e 86±3 = 12,8%; P=0,41). Conclui-se que a maior concentração de AGNE no dia 44 pós-parto em vacas Holandesas não influenciou as concentrações de &#946;-hidroxibutirato e de glicose, assim como a qualidade e a produção in vitro de embriões. No entanto, o aumento dos dias pós-parto incrementou as concentrações de glicose e reduziu a quantidade de oócitos grau I de vacas holandesas submetidas à OPU/PIV até 90 dias após o parto. / The present study evaluated the influence of the days postpartum and the concentrations of non-esterified fatty acids (NEFA - High vs. Low) on concentrations of metabolites (&#946;-hydroxybutyrate and glucose), oocyte quality and in vitro embryo production of Holstein cows during early lactation (90 days postpartum). The experiment was carried out in a commercial dairy farm (Santa Rita - Agrindus S/A), located at Descalvado - SP. At the calving moment, 30 Holstein cows were selected to be submitted to ovum pick-up (OPU) procedures each 14 days, in 5 different moments during the early lactation (30 ± 3, 44 ± 3, 58 ± 3, 72 ± 3 and 86 ± 3 days postpartum). Previously to the OPU session blood samples were collected for metabolite assay, body condition score (BCS) was recorded and the number of follicles able to be aspirated was also registered. The High and Low concentration of NEFA were stablished with the samples of day 44 ± 3 postpartum. The laboratory procedures for in vitro embryo production (in vitro maturation, fertilization and culture) were performed in the same laboratory (Bioembryo, Bauru - SP). Statistical analysis was performed by the GLM procedure of SAS. No effect was observed for different NEFA concentrations (High NEFA = 0.45 vs. Low NEFA = 0.52 mmol / L, P = 0.20), nor for days postpartum (30±3 = 0.54; 44±3 = 0.43; 58±3 = 0.43; 72±3 = 0.52 e 86±3 = 0.51 mmol/L; P=0.11) on &#946;-hydroxybutyrate concentrations. Considering glucose concentrations there was no treatment effect (High NEFA = 61.1 vs. Low NEFA = 63.6 mg / dL, P = 0.26). However, the glucose concentrations were influenced by days postpartum (30±3 = 60.1; 44±3 = 63.0; 58±3 = 63.5; 72±3 = 62.1 e 86±3 = 63.0 mg/dL; P=0.03). Treatment (High vs. Low NEFA) did not impact the number of recruited follicles (P = 0.36), total oocytes recovered (P = 0.28) and viable oocytes (P = .25). As well as, time did not alter the amount of recruited follicles (P = 0.87), total oocytes recovered (P = 0.42) and viable oocytes (P = .44). The amount of grade I oocytes was not influenced by treatment (High NEFA vs. Low NEFA, P = 0.14). However, days postpartum reduced the quantity of grade I oocytes (P = 0.05). Also, no treatment effect (High and Low NEFA) was observed for number of cleaved oocytes per OPU session (P = 0.45) and cleavage rate (P = 0.95). In the same way, days postpartum had no influence in the amount of cleaved oocytes per OPU session (P = 0.31) and cleavage rate (P = 0.80). In addition, for the in vitro embryo production, the NEFA concentrations (High NEFA = 0.4 vs. Low NEFA = 1.2, P = 0.37) and days postpartum (30±3 = 0.4; 44±3 = 0.7; 58±3 = 0.8; 72±3 = 0.9 e 86±3 = 1.2; P=0.39) did not affect the number of blastocysts per OPU session. Also, the blastocyst rate was not influenced by treatment (High NEFA = 6.2% vs. Low NEFA = 11.6%, P = 0.51) and days postpartum (30±3 = 4.8%; 44±3 = 8.9%; 58±3 = 10.7%; 72±3 = 10.0% e 86±3 = 12.8%; P=0.41). It was concluded that high concentration of NEFA on day 44 postpartum in Holstein cows did not alter the concentrations of &#946;- hydroxybutyrate and glucose, as well as, the oocyte quality and in vitro embryo production. However, the increase in days postpartum elevated the glucose concentrations and decreased the number of grade I oocytes of Holstein cows submitted to OPU and in vitro embryo production up to 90 days postpartum.

<p>ABSTRACT</p><p>A defect implantation process is the major reason for unexplained infertility. Estrogen andprogesterone are steroid hormones preparing the endometrium for implantation. They mediatetheir effect through their receptors: estrogen receptor alpha and beta and progesteronereceptor A and B, respectively. Leukemia inhibitory factor (LIF), which is also important forimplantation, mediates its effect through LIF receptor and the coreceptor, gp130, and is downregulated by suppressors of cytokine signaling 1. The aim of the study was to compare thelevels of the steroid hormone receptors and LIF related factors in the endometrium of twogroups of women with the diagnosis unexplained infertility: one that became pregnant afterassisted reproduction and one that did not become pregnant. Before treatment of thesewomen, endometrial mRNA was collected during the window of implantation in themenstrual cycle. The levels of specific mRNAs were measured with real-time PCR. Womenwho had become pregnant had a significantly higher level of steroid hormone receptors. Thus,these proteins seem to be important for a pregnancy and may be suitable as receptivitymarkers.</p>

Although the mechanisms underlying the divergence of the first cell types in the mouse, the trophectoderm (TE) and the inner cell mass (ICM) have received considerable attention, the upstream signals stimulating their divergence are not well understood. The work presented here examines the roles that morphogenetic factors such as cell adhesion and polarization play in the development of these cell types. I show here that in embryos completely lacking both maternal and zygotic E-cadherin, the normal epithelial morphology of outer cells is disrupted but individual cells still initiate TE and ICM-like fates. A larger proportion of cells than normal expressed TE markers like Cdx2 (a homeodomain containing transcription factor), suggesting that formation of an organized epithelium is not necessary for TE-specific gene expression. Individual cells in such embryos still generate an apical-like domain that correlates with elevated Cdx2 expression. I also show that repolarization can occur in isolated early ICMs from both wild type and Cdx2 mutant embryos, indicating that Cdx2 is not required to initiate polarity. Importantly, I demonstrate a critical role for the Rho-associated kinase ROCK in apical-basal polarization of preimplantation blastomeres. Loss of apical-basal polarization leads to a reduction of Cdx2 expression in outer blastomeres due to activation of Lats1/2 kinase and reduced nuclear Yap1. The influence of polarization upon Lats1/2 kinase is stage-dependent however, as apolar 8-cell blastomeres retain nuclear Yap1. Cell position appears to serve as an additional cue for nuclear localization of Yap and Cdx2 expression from the 8-cell stage to E3.5. Cell polarization plays an additional role in the embryo of maintaining cells in consistently outer or inner positions, thus ensuring that Cdx2 is expressed exclusively in the developing TE. The results of this work demonstrate important links between morphogenesis, cell fate and patterning in the preimplantation embryo. Both cell polarization and cell position act as critical cues to determine gene expression and to pattern this expression within the embryo.

Although the mechanisms underlying the divergence of the first cell types in the mouse, the trophectoderm (TE) and the inner cell mass (ICM) have received considerable attention, the upstream signals stimulating their divergence are not well understood. The work presented here examines the roles that morphogenetic factors such as cell adhesion and polarization play in the development of these cell types. I show here that in embryos completely lacking both maternal and zygotic E-cadherin, the normal epithelial morphology of outer cells is disrupted but individual cells still initiate TE and ICM-like fates. A larger proportion of cells than normal expressed TE markers like Cdx2 (a homeodomain containing transcription factor), suggesting that formation of an organized epithelium is not necessary for TE-specific gene expression. Individual cells in such embryos still generate an apical-like domain that correlates with elevated Cdx2 expression. I also show that repolarization can occur in isolated early ICMs from both wild type and Cdx2 mutant embryos, indicating that Cdx2 is not required to initiate polarity. Importantly, I demonstrate a critical role for the Rho-associated kinase ROCK in apical-basal polarization of preimplantation blastomeres. Loss of apical-basal polarization leads to a reduction of Cdx2 expression in outer blastomeres due to activation of Lats1/2 kinase and reduced nuclear Yap1. The influence of polarization upon Lats1/2 kinase is stage-dependent however, as apolar 8-cell blastomeres retain nuclear Yap1. Cell position appears to serve as an additional cue for nuclear localization of Yap and Cdx2 expression from the 8-cell stage to E3.5. Cell polarization plays an additional role in the embryo of maintaining cells in consistently outer or inner positions, thus ensuring that Cdx2 is expressed exclusively in the developing TE. The results of this work demonstrate important links between morphogenesis, cell fate and patterning in the preimplantation embryo. Both cell polarization and cell position act as critical cues to determine gene expression and to pattern this expression within the embryo.

The mammalian embryo is encased in a glycoproteinaceous covering, the zona pellucida (ZP/zona) during preimplantation development. Prior to implantation into the recipient maternal endometrium, the blastocyst has to hatch out of this zona. This is a critical and an important event for the successful establishment of pregnancy. Hatching in mammals is characterised by the expansion of the blastocyst, followed by the nicking of the zona and extrusion of the blastocyst by repeated contraction-expansion cycles, thereby leaving the empty zona behind. In species such as the mouse, cow and primates, the empty zona is left behind in the uterine lumen. However, in the hamsters, the features associated with hatching are characteristic for this species. Firstly, the blastocyst remains predominantly in a deflated state. Secondly, the zona undergoes focal rupture which is followed by the complete dissolution of the zona. Third, trophectodermal projections (TEPs) present in the blastocysts, aid the hatching of the blastocyst. Hence, this study was aimed to identify the molecular players involved in hamster blastocyst hatching and to study their embryo-endometrial expression. Earlier work in the laboratory has demonstrated the involvement of cysteine protease-like factors in hamster blastocyst hatching (Mishra and Seshagiri, 2000a). Broad spectrum cysteine protease inhibitors, E-64 and PHMB, completely blocked the hatching of blastocysts. To identify the class of cysteine proteases involved in this phenomenon, class-specific inhibitors were used in this study. Calpain and caspase inhibitors, calpastatin and Z-VAD- FMK, respectively, did not block hamster blastocyst hatching (Fig 2.2). Cathepsin (cts)-specific inhibitors, cystatin-C and peptidyl diazomethane (PPDM) blocked hatching of embryos in a dose-, time- and embryo-stage dependant manner (Figs 2.5, 2.6, 2.10 and 2.11). Continuous exposure of 1.0 µM cystatin to expanded or deflated blastocysts completely blocked hatching (Fig 2.3Aii, iii), without effecting their viability (Fig 2.3Bii and iii). Deflated blastocysts exposed transiently to 1.0 µM cystatin, for 12 or 6 h failed to hatch, but could overcome the inhibition and exhibited hatching, when transferred to fresh, inhibitor-free medium (Fig 2.6). Effect of the inhibitor was less pronounced in the deflated blastocysts when compared to expanded blastocysts (Figs 2.5 and 2.6). The viability of the cystatin-treated embryos was not affected as assessed by vital-dye staining and also their ability to attach and exhibit trophoblast (TB) proliferation on serum-coated dishes was not compromised. The area of the TB outgrowth of cystatin-treated embryos was similar to that of the untreated embryos (Fig 2.9). The inhibitory effect of PPDM, an irreversible inhibitor of cts, on blastocyst hatching was demonstrated. Expanded and deflated blastocysts exhibited a dose-dependent inhibition in hatching, following the exposure to 0.5 and 1.0 µM of PPDM (Figs 2.10A and 2.11A). When treated with the inhibitor for 6 or 12 h, there was a transient inhibition in hatching, as blastocysts could overcome the inhibition and exhibit hatching following transfer to inhibitor-free, fresh medium. Inhibitor-treated hatched blastocysts, when transferred to serum-coated dishes, attached and exhibited TB outgrowth, similar to untreated embryos (Figs 2.13 and 2.14). A PPDM-interacting protease was localised to the cytoplasm of the embryonic cells in the hamster blastocyst, suggesting that the embryo is the source of the zona lysin. Two forms of the enzyme, a probable variant zymogen of molecular mass 65 k and an active form of molecular mass 32 k were detected in the blastocysts (Fig 2.15). In vitro susceptibility of hamster zona to cathepsins is significantly different from that of other species zonae such as the mouse, rat, monkey and human zonae (Table 2.2). All these lines of evidence unequivocally demonstrate the involvement of cathepsins in hamster blastocyst hatching, which is in sharp contrast to what is observed in the mouse, where serine proteases such as strypsin/hepsin, ISP-1 and -2 are reported to play an important role in blastocyst hatching. However, since extensive inhibitor studies were not performed using embryos from other species, it is possible that cysteine proteases maybe involved in the hatching of blastocysts from other species. Having shown the role of cathepsins in hamster zona dissolution, expression of the cathepsins in preimplantation embryos was investigated. Hamster specific cts–L, -B and –P were amplified from day 14 placenta using mouse primers and the amplicons were found to be highly homologous to the cts of other species (Fig 3.2). Hamster and mouse preimplantation embryos i.e., 8-cell, morula and blastocyst were found to express cts–L, -B and –P transcripts (Figs 3.6 and 3.10). Cts-P, present only in the TBs of the placenta (Fig 3.4), for the first time, was also shown to be present in the preimplantation embryos. The immunoreactive cts-L and -P proteins were detected in blastomeres of 8-cell embryo, in the inner cell mass (ICM) and trophectoderm (TE) of the blastocyst (Figs 3.7 and 3.8). These cathepsins could probably correspond to the PPDM- interacting enzymes of molecular mass 32 and 65 kDa, described above. (fig) Fig 5.1. Overview of the expression and the role of embryo-endometrial cathepsins in blastocyst hatching in the golden hamster. Cathepsins ( ) produced by the inner cell mass ( ) or the trophectoderm ( ) of the blastocyst or the endometrial cells ( ) act on the zona matrix ( ), bringing about its lysis. The cathepsins are secreted into the peri-vitelline space or are carried by trophectodermal projections (TEPs, yellow projections) to the zona. Also shown are endogenous inhibitors and growth factors that can regulate these cathepsins. A striking observation made in this study was the detection of the immunoreactive signals for cathepsins in the zona matrix of blastocysts. Since hamster blastocysts possess extracellular projections (TEPs), it is possible for these projections to participate in the transport of cathepsins from TE cells to the zona; as the localisation of the proteases to these projections was demonstrated (Fig 3.9). Also, since the actin-based projections are highly undulating structures, they might potentiate the mechanical rupture of the zona during hatching, apart from acting as carriers for the proteases. Hence, during hatching of the hamster blastocyst, cathepsins, expressed in the ICM and the TE, might be secreted transiently into the peri-vitelline space, whereby they can act on the ZP. Alternatively, in the absence of any apoptotic cells in the embryo that can release the cell contents (Fig 3.13), the cathepsins may be deposited by TEPs in specific pockets of the zona matrix, thereby causing focal zona lysis. In vivo, the hatching of the blastocysts is brought about by both embryonic and maternal proteases. Cts–L and -B transcripts were detected in the maternal endometrium during different stages of the reproductive cycle and early pregnancy (Fig 4.1 and 4.3). Immunoreactive cts-L protein was detected in the uterine luminal epithelium and the stromal cells (Fig 4.5). In the uterus, the PPDM-interacting 32 kDa form was in abundance compared to the 65 kDa form (Fig 4.6). Hence, uterine cathepsins might play a major role in the remodelling of the extracellular matrix during estrous cycle and pregnancy. However, the role of these cathepsins in causing zona dissolution during blastocyst hatching, along with embryonic proteases cannot be ruled out. Reports of recurrent miscarriages in women with low serum cystatin levels imply a role for cysteine proteases in early pregnancy events like blastocyst development, hatching and implantation. Hence, these studies, described in the thesis, could form a basis to investigate the role of cathepsins in early human development. Taken together, the results demonstrate the involvement of embryo-derived cathepsins in hamster blastocyst hatching. These cathepsins may be secreted into the peri-vitelline space or transported to the zona matrix by TEPs (Fig 5.1). Additionally, in vivo, endometrial cathepsins might aid the embryonic zona lysins in the complete zona dissolution. The regulation of these proteases by growth factors, cytokines and their specific inhibitors needs to be explored. (For figure pl see the original document)

ABSTRACT A defect implantation process is the major reason for unexplained infertility. Estrogen andprogesterone are steroid hormones preparing the endometrium for implantation. They mediatetheir effect through their receptors: estrogen receptor alpha and beta and progesteronereceptor A and B, respectively. Leukemia inhibitory factor (LIF), which is also important forimplantation, mediates its effect through LIF receptor and the coreceptor, gp130, and is downregulated by suppressors of cytokine signaling 1. The aim of the study was to compare thelevels of the steroid hormone receptors and LIF related factors in the endometrium of twogroups of women with the diagnosis unexplained infertility: one that became pregnant afterassisted reproduction and one that did not become pregnant. Before treatment of thesewomen, endometrial mRNA was collected during the window of implantation in themenstrual cycle. The levels of specific mRNAs were measured with real-time PCR. Womenwho had become pregnant had a significantly higher level of steroid hormone receptors. Thus,these proteins seem to be important for a pregnancy and may be suitable as receptivitymarkers.

CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior / The Binder of Sperm Protein 1 (BSP1) is a protein produced by seminal vesicles of animals. It helps into the fertilization process of oocytes, promoting sperm capacitation, mediating the ligation from itself with the oviduct epithelium, and increasing the motility in the oviduct. When spermatozoa with purified BSP1 were incubated, acrosomal reaction rates were determined with and without the presence of heparin, as controls. The percentage of acrosomal reaction was higher (p <0.05) in control 1 (44.5%) compared with the other treatments (BSP1:10 Âg/mL: 24.5%; 20 Âg/mL: 25.5%; 40 Âg/mL: 26.0 %), and lower the rate (p> 0.05) when sperm were incubated only in Fert-TALP medium without heparin (14.5%). Cleavage and blastocyst rates were evaluated on days two and seven respectively, after fertilize oocytes in a medium containing BSP1. 1274 cumulus- oocyte complexes were recovered and incubated for 18 hours with frozen-thawed ejaculated semen in a Fert-TALP medium, containing: only heparin, 10, 20 or 40 &#956;g/mL of BSP1. Cleavage and blastocyst rates (34.1  4.4 vs 40.8  5.0%) were similar (p> 0.05) when incubation was made with 10 Âg/mL of BSP1 and heparin, respectively. However, the concentrations of 20 and 40 Âg/mL decreased the formation of blastocysts (22.4  2.9 and 19.3  4.1%) compared with heparin (40.8  5.1%, p <0.02). Subsequently, cumulus- oocyte complexes (n = 2239) were incubated with frozen-thawed ejaculated semen. Spermatozoa were selected by a gradient of 45% -90% Percoll containing: only heparin, 10, 20, 40 &#956;g/mL of BSP1 and there was a control 2 of Percoll without heparin or BSP1. Cleavage rate was similar (p> 0.05) for the incubation with concentrations of 10, 20 and 40 &#956;g/mL of BPS1 (67.7  3.0, 68.7  3.5, 75.2  3.8, respectively). However, these rates were similar when it was used just heparin and when oocytes were incubated with 40Âg/mL of BSP1 (78.9  1.7 vs 75.2  3.8%). For blastocyst rates was found that they were similar (p> 0.05) when the selection was made with heparin (44.1  4.3%) and 40 Âg/mL of BSP1 (30.0  3.3%). Finally, 1213 cumulus-oocyte complexes were recovered and incubated with freeze-thawed epididymal semen in Fert-TALP medium, which contained: only heparin, with heparin, and 10, 20 or 40 Âg/mL of BSP1. Cleavage and blastocyst rates were similar after incubation with and without heparin, but the concentration of 40Âg/mL of BSP1 produced higher cleavages rates (79.0  1.1%) than control 1 (68.5  1.3%, p <0.05). About blastocyst rates, there were rates significantly higher when concentrations of 20 and 40 Âg/mL of BSP1 were used (35.6  2.5 and 41.1  2.0%) than with (24.7  3.2; p <0.05) and without heparin (27.3  1.6%; p <0.0003). In conclusion, BSP1 allowed proper cleavage and development, when the protein was added to the fertilization medium and the Percoll gradient using ejaculated semen, and to the fertilization medium when used epididymal sperm, without requiring the use of heparin. / A âBinder of Sperm Protein 1â (BSP1) à uma proteÃna produzida pelas vesÃculas seminais dos animais, que ajuda no processo de fertilizaÃÃo do oÃcito promovendo a capacitaÃÃo espermÃtica, mediando a sua ligaÃÃo com o epitÃlio do oviduto e aumentando sua motilidade no oviduto. As taxas de reaÃÃo de acrossoma dos espermatozoides foram determinadas ao serem incubados com BSP1 purificado, e com e sem a presenÃa de heparina, como controles. A porcentagem de reaÃÃo de acrossoma foi maior (p<0.05) no controle 1 (44.5%) comparado com os tratamentos restantes (BSP1: 10 Âg/mL: 24.5%; 20 Âg/mL: 25.5%; 40 Âg/mL: 26.0%), sendo menor esta taxa (p>0.05) quando os espermatozoides sà foram incubados no meio Fert-TALP sem heparina (14.5%). As taxas de clivagem e de blastocistos foram avaliadas nos dias dois e sete respectivamente, depois de fertilizar oÃcitos em um meio que continha BSP1. Foram recuperados 1274 COCs e incubados durante 18 horas com sÃmen ejaculado congelado- descongelado em meio Fert-TALP, que continha: sà heparina, 10, 20 ou 40 Âg/mL de BSP1. As taxas de clivagem e de blastocistos (34.1  4.4 vs 40.8  5.0%) foram similares (p>0.05) quando se fez a incubaÃÃo com 10 Âg/mL de BSP1 e heparina, respectivamente. PorÃm, as concentraÃÃes de 20 e 40 Âg/mL diminuÃram a formaÃÃo de blastocistos (22.4  2.9 e 19.3  4.1%) em relaÃÃo com a heparina (40.8  5.1%; p < 0.02). Posteriormente foram incubados COCs (n= 2239), com sÃmen ejaculado congelado-descongelado que foi selecionado por um gradiente de Percoll 45%-90% que continha: sà heparina, 10, 20 ou 40 Âg/mL de BPS1 e foi realizado um controle 2 de Percoll sem heparina nem BSP1. A taxa de clivagem foi similar (p > 0.05) para a incubaÃÃo com as concentraÃÃes de 10, 20 e 40 Âg/mL de BSP1 (67.7Â3.0, 68.7Â3.5, 75.2Â3.8). PorÃm, estas taxas foram similares quando sà foi usada heparina e quando se incubou com 40 Âg/mL de BSP1 (78.9Â1.7 vs 75.2Â3.8%). Para as taxas de blastocistos encontrou-se que foram similares (p > 0.05) quando se fez a seleÃÃo com heparina (44.1Â4.3%) e com 40 Âg/mL de BSP1 (30.0Â3.3%). Finalmente, foram recuperados 1213 complexos cumulus-oÃcitos e incubados com espermatozoides epididimÃrios congelados-descongelados em meio Fert-TALP, que continham: sà heparina, sem heparina, e 10, 20 ou 40 Âg/mL de BSP1. As taxas de clivagem e de blastocistos foram similares apÃs as incubaÃÃes com e sem heparina, mas a concentraÃÃo de 40 Âg/mL de BSP1 produziu maiores taxas de clivagem (79.0  1.1%) que o controle 1 (68.5  1.3%; p < 0.05). Quanto Ãs taxas de blastocistos, encontraram-se maiores taxas quando foram usadas as concentraÃÃes de 20 e 40 Âg/mL de BSP1 (35.6  2.5 e 41.1  2.0%) que com (24.7  3.2; p < 0.05) e sem heparina (27.3  1.6%; p < 0.0003). Em conclusÃo, a BSP1 adicionada ao meio de fertilizaÃÃo e ao gradiente de Percoll quando usado o sÃmen ejaculado, e ao meio de fertilizaÃÃo quando usados espermatozoides epididimÃrios, permitiu clivagem e desenvolvimento prÃprio, sem a necessidade do uso de heparina.

Submitted by Mario BC (mario@bc.ufrpe.br) on 2017-05-04T12:12:28Z No. of bitstreams: 1 Pabola Santos Nascimento.pdf: 865543 bytes, checksum: 47ce2118a4d55e4ada483756d00b9ae6 (MD5) / Made available in DSpace on 2017-05-04T12:12:28Z (GMT). No. of bitstreams: 1 Pabola Santos Nascimento.pdf: 865543 bytes, checksum: 47ce2118a4d55e4ada483756d00b9ae6 (MD5) Previous issue date: 2014-08-28 / The use of sexed semen for in vitro embryo production (IVP) is a potentially effective means for obtaining the progeny with predetermined sex. For years, animal owners wanted a methodology that pre determine the sex of offspring for their herds. Rates of cleavage, morula and blastocyst seem to be affected not only by the damages caused by sexing, but it is believed that the bull factor, and other aspects that have not been fully elucidated, directly influencing its successful use. The aim of this study was to evaluate the influence of type of semen (sexed /conventional) and a bull factor over blastocyst rates when submitting bovine oocytes obtained from slaughterhouse to IVP, and also compare these results with analyzes of sperm kinetics. Oocytes (n = 959) were matured, fertilized with sexed and non-sexed semen from three 5/8 Girolando bulls. A straw of each type of semen was assessed with use of "computer-assisted semen analysis" (CASA) and fluorescence microscopy. Three replicates were performed during the experiment. Data were analyzed by SPSS 16.0 statistical program employing analysis of variance (ANOVA). The Student t test was used to detect differences between groups. The Chi-square test was used to analyze the results of embryo production. For all analyzes, values were considered significant (P <0.05). The results differed between sexed (21.10%) and non-sexed semen (31.06%) to blastocysts production. We conclude that in the present work sexed semen was less efficient in producing blastocyst when comparing non-sexed semen of the same bulls and when comparing semen types (sexed and non-sexed) from the same bull. Analyses of sperm kinetics and fluorescent probes were compatible with the fertilizing potential of samples of sexed and non-sexed semen of 5/8 Girolando bulls. / O uso de sêmen sexado em conjunto com a produção in vitro (PIV) de embriões é um meio potencialmente eficiente na obtenção da descendência com sexo predeterminado. Há anos, os proprietários dos animais desejaram uma metodologia que pré determinasse o sexo da prole para seus rebanhos. As taxas de clivagem, mórula e blastocisto parecem ser afetadas não só pela debilitação provocada na sexagem, mas acredita-se que pelo reprodutor em questão, e por outros fatores que não foram ainda totalmente elucidados, influenciando diretamente na sua utilização com sucesso. O objetivo desse trabalho foi avaliar a influencia do tipo de sêmen (sexado/convencional) e do touro, nas taxas de blastocisto na PIV de oócitos bovinos obtidos em matadouro, e ainda comparar esses resultados com as análises da cinética espermática. Oócitos (N= 959) foram maturados, fertilizados com sêmen sexado e convencional de três touros da raça 5/8 Girolando. Uma palheta de cada tipo de sêmen foi avaliada com uso da “computer-assisted sêmen analysis” (CASA) e da microscopia de fluorescência. Foram realizadas três repetições durante o experimento. Os dados foram analisados pelo programa estatístico SPSS 16.0 empregando-se a análise de variância (ANOVA). O teste t-Student foi usado para detectar diferenças entre os grupos. O Qui-quadrado foi utilizado para análise dos resultados da produção de embriões. Para todas as análises, os valores foram considerados significativos (P< 0,05). Os resultados diferiram entre o sêmen convencional (31,06) e sexado (21,10%) para produção de blastocisto. Quando comparamos a produção de blastocisto individualmente nas amostras de sêmen sexado (27,69%; 17,93% e 25,56%, touros 1, 2 e 3 respectivamente) percebemos que T2 < T1 e T1=T3 e T2=T3. Concluimos que no presente trabalho o sêmen sexado foi menos eficiente na produção de blastocisto quando comparado ao sêmen convencional de forma geral e do mesmo touro. As análises da cinética espermática bem como as sondas fluorescentes foram compatíveis com o potencial fertilizante das amostras de sêmen sexado e convencional em touros da raça 5/8 Girolando.

O presente estudo avaliou a influência das concentrações de ácidos graxos não esterificados (AGNE Alto vs. Baixo) no dia 44±3 pós-parto, e dos dias pós-parto nas concentrações de metabólitos (&#496;-hidroxibutirato e glicose) e na qualidade oocitária e produção in vitro de embriões de vacas Holandesas no início da lactação (até 90 dias pós-parto). O experimento foi realizado na Fazenda Santa Rita (Agrindus S/A) localizada no município de Descalvado SP. A partir da data do parto foram selecionadas 30 vacas Holandesas para serem aspiradas a cada 14 dias em cinco diferentes momentos no início da lactação (30±3, 44±3, 58±3, 72±3 e 86±3 dias pós-parto). No momento da aspiração folicular (OPU), foram realizadas as colheitas de sangue para dosagem dos metabólitos, a avaliação do escore de condição corporal (ECC) e a contagem dos folículos visualizados. Os procedimentos de produção in vitro de embriões (maturação, fertilização e cultivo) foram realizados no laboratório da Bioembryo, localizado no município de Bauru - SP. A análise estatística foi realizada pelo procedimento GLM do SAS. Não se observou efeito de tratamento (Alto AGNE = 0,45 vs. Baixo AGNE = 0,52 mmol/L; P=0,20) e de tempo (30±3 = 0,54; 44±3 = 0,43; 58±3 = 0,43; 72±3 = 0,52 e 86±3 = 0,51 mmol/L; P=0,11) para as concentrações de &#946;-hidroxibutirato. Para as concentrações de glicose não se verificou efeito do tratamento (Alto AGNE = 61,1 vs. Baixo AGNE = 63,6 mg/dL; P=0,26). No entanto, observou-se efeito de tempo para as concentrações de glicose (30±3 = 60,1; 44±3 = 63,0; 58±3 = 63,5; 72±3 = 62,1 e 86±3 = 63,0 mg/dL; P=0,03). O tratamento (Alto vs. Baixo AGNE) não influenciou a quantidade de folículos recrutados (P=0,36), oócitos totais recuperados (P=0,28) e oócitos viáveis (P=0,25). Assim como o tempo não alterou a quantidade de folículos recrutados (P=0,87), oócitos totais recuperados (P=0,42) e oócitos viáveis (P=0,44). A quantidade de oócitos grau I não foi influenciada pelo tratamento (Alto vs. Baixo AGNE; P=0,14). Porém, os dias pós-parto reduziram a sua quantidade (P=0,05). A quantidade de oócitos clivados por vaca aspirada (P=0,45) e a taxa de clivagem (P=0,95) não apresentaram diferenças estatísticas conforme as concentrações de AGNE (Alto vs. Baixo) no dia 44 pós-parto. Os dias pós-parto também não alteraram a quantidade de oócitos clivados por vaca aspirada (P=0,31) e a taxa de clivagem (P=0,80). Para a produção in vitro de embriões, a quantidade de blastocisto por vaca aspirada conforme as concentrações de AGNE (Alto = 0,4 vs. Baixo = 1,2; P=0,37) e os dias pós-parto (30±3 = 0,4; 44±3 = 0,7; 58±3 = 0,8; 72±3 = 0,9 e 86±3 = 1,2; P=0,39) não apresentaram diferenças estatísticas. Assim como, a taxa de blastocisto para os animais dos grupos (Alto AGNE = 6,2% vs. Baixo AGNE = 11,6%; P=0,51) e para os diferentes momentos pós-parto (30±3 = 4,8%; 44±3 = 8,9%; 58±3 = 10,7%; 72±3 = 10,0% e 86±3 = 12,8%; P=0,41). Conclui-se que a maior concentração de AGNE no dia 44 pós-parto em vacas Holandesas não influenciou as concentrações de &#946;-hidroxibutirato e de glicose, assim como a qualidade e a produção in vitro de embriões. No entanto, o aumento dos dias pós-parto incrementou as concentrações de glicose e reduziu a quantidade de oócitos grau I de vacas holandesas submetidas à OPU/PIV até 90 dias após o parto. / The present study evaluated the influence of the days postpartum and the concentrations of non-esterified fatty acids (NEFA - High vs. Low) on concentrations of metabolites (&#946;-hydroxybutyrate and glucose), oocyte quality and in vitro embryo production of Holstein cows during early lactation (90 days postpartum). The experiment was carried out in a commercial dairy farm (Santa Rita - Agrindus S/A), located at Descalvado - SP. At the calving moment, 30 Holstein cows were selected to be submitted to ovum pick-up (OPU) procedures each 14 days, in 5 different moments during the early lactation (30 ± 3, 44 ± 3, 58 ± 3, 72 ± 3 and 86 ± 3 days postpartum). Previously to the OPU session blood samples were collected for metabolite assay, body condition score (BCS) was recorded and the number of follicles able to be aspirated was also registered. The High and Low concentration of NEFA were stablished with the samples of day 44 ± 3 postpartum. The laboratory procedures for in vitro embryo production (in vitro maturation, fertilization and culture) were performed in the same laboratory (Bioembryo, Bauru - SP). Statistical analysis was performed by the GLM procedure of SAS. No effect was observed for different NEFA concentrations (High NEFA = 0.45 vs. Low NEFA = 0.52 mmol / L, P = 0.20), nor for days postpartum (30±3 = 0.54; 44±3 = 0.43; 58±3 = 0.43; 72±3 = 0.52 e 86±3 = 0.51 mmol/L; P=0.11) on &#946;-hydroxybutyrate concentrations. Considering glucose concentrations there was no treatment effect (High NEFA = 61.1 vs. Low NEFA = 63.6 mg / dL, P = 0.26). However, the glucose concentrations were influenced by days postpartum (30±3 = 60.1; 44±3 = 63.0; 58±3 = 63.5; 72±3 = 62.1 e 86±3 = 63.0 mg/dL; P=0.03). Treatment (High vs. Low NEFA) did not impact the number of recruited follicles (P = 0.36), total oocytes recovered (P = 0.28) and viable oocytes (P = .25). As well as, time did not alter the amount of recruited follicles (P = 0.87), total oocytes recovered (P = 0.42) and viable oocytes (P = .44). The amount of grade I oocytes was not influenced by treatment (High NEFA vs. Low NEFA, P = 0.14). However, days postpartum reduced the quantity of grade I oocytes (P = 0.05). Also, no treatment effect (High and Low NEFA) was observed for number of cleaved oocytes per OPU session (P = 0.45) and cleavage rate (P = 0.95). In the same way, days postpartum had no influence in the amount of cleaved oocytes per OPU session (P = 0.31) and cleavage rate (P = 0.80). In addition, for the in vitro embryo production, the NEFA concentrations (High NEFA = 0.4 vs. Low NEFA = 1.2, P = 0.37) and days postpartum (30±3 = 0.4; 44±3 = 0.7; 58±3 = 0.8; 72±3 = 0.9 e 86±3 = 1.2; P=0.39) did not affect the number of blastocysts per OPU session. Also, the blastocyst rate was not influenced by treatment (High NEFA = 6.2% vs. Low NEFA = 11.6%, P = 0.51) and days postpartum (30±3 = 4.8%; 44±3 = 8.9%; 58±3 = 10.7%; 72±3 = 10.0% e 86±3 = 12.8%; P=0.41). It was concluded that high concentration of NEFA on day 44 postpartum in Holstein cows did not alter the concentrations of &#946;- hydroxybutyrate and glucose, as well as, the oocyte quality and in vitro embryo production. However, the increase in days postpartum elevated the glucose concentrations and decreased the number of grade I oocytes of Holstein cows submitted to OPU and in vitro embryo production up to 90 days postpartum.