Tem se tornado evidente que a iniciação e a progressão do câncer depende de vários componentes do microambiente tumoral, incluindo células inflamatórias e imunes (linfócitos, macrófagos e mastócitos), fibroblastos, células endoteliais, adipócitos e matriz extracelular. De maneira geral, esses componentes são conhecidos como estroma. Tanto interações pró- como anti-tumor ocorrem entre um câncer e suas células vizinhas. Em um estudo prévio, avaliamos dados de bibliotecas SAGE de carcinoma epidermóide de cabeça e pescoço (CECP) usando ferramentas estatísticas e de bioinformática e pudemos identificar os genes mais e menos expressos em tumores metastáticos versus não metastáticos e em tumores versus tecidos normais. Em outro estudo, avaliamos fatores parácrinos solúveis produzidos por células do estroma e por células neoplásicas que poderiam influenciar proliferação e expressão gênica e protéica. Ambos os estudos identificaram marcadores potenciais associados a respostas inflamatórias ou imunes. Dezenove desses genes foram selecionados por PCR em tempo real e o estudo foi realizado nas linhagens SCC-9 de células epiteliais neoplásicas e de fibroblastos isolados de um câncer oral, e em 40 amostras de carcinomas primários de cabeça e pescoço (6 amostras micro e 34 macrodissecadas). Nós também utilizamos eletroforese unidimensional para analisar a expressão protéica nesse conjunto de amostras. Como a microdissecção produziu baixas concentrações de RNA e proteínas, ciclos extras de amplificação de mRNA foram necessários para obter material suficiente para experimentos de PCR. Nossos dados mostraram que os perfis de expressão foram provavelmente pouco preservados durante os ciclos extras de amplificação. Em amostras macrodissecadas, nós consistentemente observamos que o nível de transcritos de MGLL, COX2, EP3, EP4 e LTAH4 estava reduzido, porém presente nas suas margens cirúrgicas. Os dados não confirmaram, em células de CECP, a hipótese de que MGLL produz menssageiros lipídicos oncogênicos, esta via pode não atuar nesses pacientes. Nós também observamos que metaloproteinases são expressas em níveis elevados em CECP e devem estar envolvidas na degradação da matriz extracelular. Células neoplásicas e do estroma desses carcinomas exibem uma ampla variedade de proteínas com níveis muito diferentes de expressão. Este resultado abre perspectivas para realização de experimentos de validação / It has become evident that cancer initiation and progression depends on several components of the tumor microenvironment, including inflammatory and immune cells (lymphocytes, macrophages and mastocytes), fibroblasts, endothelial cells, adipocytes, and extracellular matrix. Collectively, these components are known as the stroma. Both pro- and anti-tumor interactions occur between a tumor and its surrounding cells. In a previous study, we evaluated data from SAGE libraries of head and neck squamous cell carcinoma (HNSCC) using statistical and bioinformatic tools and we could identify top-up and top-downregulated genes in metastatic versus non-metastatic tumors and in tumors versus normal tissues. In another study, we evaluated soluble paracrine factors produced by stromal and neoplastic cells which may influence proliferation and gene and protein expression. Both studies identified potential markers associated with immune or inflammatory response in head and neck tumorigenesis. Nineteen of these genes were selected for real-time polymerase chain reaction (PCR) and the study was carried out on the epithelial cancer cell line SCC-9 and on fibroblasts isolated from an oral cancer, and in 40 samples from primary HNSCC (6 micro and 34 macrodissected samples). We also used one-dimensional gel electrophoresis and mass spectrometry to analyze protein expression in this set of samples. As microdissection yielded low RNA and protein concentrations, extra rounds of mRNA amplification were necessary to obtain sufficient material for PCR experiments. Our data showed that expression profiles were probably scantily preserved during the extra rounds of amplification. In macrodissected samples, we consistently observed that the level of MGLL, COX2, EP3, EP4 e LTAH4 transcripts was low in most tumors but present in their surgical margins. The data do not confirm in HNSCC the hypothesis that MGLL produces oncogenic lipid messengers, this pathway may not act in these patients. We also observed that metalloproteinases are overexpressed in HNSCC and should be involved in extracellular matix degradation. Neoplastic and stromal cells from HNSCC exhibit a wide variety of proteins with very different levels of expression. This result opens the perspective to perform validation experiments.

Em bovinos, a mortalidade embrionária associada a falhas no processo de reconhecimento materno da prenhez atinge 30 a 40%. O sucesso da prenhez, depende de uma apropriada interação bioquímica entre o endométrio materno e o concepto. O objetivo dessa tese foi desenvolver uma técnica cirúrgica para monitorar o microambiente uterino de vacas cíclicas e prenhez nos dias 14 a 20 após o estro. Como objetivos específicos foram verificados se a implantação e a presença dos cateteres uterinos afetariam (1) a manutenção da prenhez, (2) a função luteal e (3) o desenvolvimento folicular. Em vacas holandesas, cíclicas e não lactantes, foram implantadas cateteres de silicone em cada corno uterino no segundo dia após o estro (fase preparatória). No dia 15 pós-estro os animais receberam uma injeção de D-clorprostenol e a ovulação foi confirmada por ultrasonografia transretal (US; dia experimental 1). No dia experimental 7, as vacas (n=6) receberam ou não (n=3) transferência de embriões via transcervical no corno uterino ipisilateral ao ovário contendo o corpo lúteo (CL). Nos dias experimentais 14, 16, 18 e 20, estruturas ovarianas foram avaliadas por US, e cada corno uterino foi lavado através dos cateteres implantados no lúmen uterino (três sessões de 6 ml cada). Amostras de sangue foram coletadas nos dias 1 a 20 da fase experimental e concentração de progesterona (P4) foi mensurada por radioimunoensaio. As vacas foram abatidas no dia experimental 20 e a prenhez diagnosticada por visualização macroscópica do concepto após a dissecação do útero. A taxa de presença do concepto no dia 20 experimental foi 0%. No dia experimental 7, um CL e um folículo grande (9 a 17 mm) estavam presentes nos ovários das vacas. A taxa de aumento da concentração de P4 entre os dias 1 a 5 foi de 0 ng/mL/dia em 7/9 vacas. Luteólise ocorreu antes do dia 15 em 3/9 vacas, entre os dias 16 e 20 foi 3/9, e após o dia 20 em 2/9 vacas. Não houve aumento de P4 na fase luteal em uma vaca. Foi verificado ovulação antes do dia 20 em 3/9 vacas. A taxa de aumento do último folículo dominante foi de 1,3mm/dia em 2/9 vacas e menor nos animais restantes. Cistos foliculares, CL sub-luteinizado e endometrite foram diagnosticados em 2/9, 2/9 e 1/9 vacas, respectivamente. Foi possível concluir que as alterações nas funções ovarianas e uterinas foram causadas pela presença e implantação dos cateteres e essas alterações foram incompatíveis com a manutenção da prenhez. A abordagem cirúrgica testada não foi adequada para estudar o microambiente uterino de vacas prenhez / In cattle, embryonic mortality associated with failure in the process of maternal recognition of pregnancy reaches 30 to 40%. Successful pregnancies depend on appropriate biochemical interactions between the maternal endometrium and conceptus. Overall objective was to develop a surgical technique to probe the uterine microenvironment of cyclic and pregnant cows days 14 to 20 post- estrus. Specific objectives were to verify whether presence and operation of uterine catheters would affect (1) maintenance of pregnancy, (2) luteal function and (3) follicular growth. Non-lactating, cyclic, Holstein cows were fitted with a silicone catheter in each uterine horn on day 2 after estrus. On day 15 they received an injection of D-cloprostenol and ovulations were confirmed by transrectal ultrasonography (US; experimental day 1). On experimental day 7, cows received (n=6) or not (n=3) embryos by trans-cervical transfer to the uterine horn ipsilateral to ovary containing the corpus luteum (CL). On experimental days 14, 16, 18 and 20, ovarian strutures were observed by US and each uterine horn was washed through the catheter (three sessions of 6 ml each). Blood samples were collected from experimental days 1 to 20 and progesterone (P4) concentrations were measured by radioimmnoassay. Cows were slaughtered on experimental day 20 and pregnancies were diagnosed by macroscopic visualization of a conceptus after dissection of uterus. Conception rate at day 20 was 0%. On experimental day 7, both a CL and a large follicle (9 to 17mm) were present in ovaries of all cows. Rate of increase of P4 concentrations from days 1 to 5 was 0ng/ml/day in 7/9 cows. Luteolysis occurred before day 15 in 3/9 cows, between days 16 and 20 in 3/9 cows and after day 20 on 2/9 cows. No luteal phase rise in P4 was noticed for one cow. Ovulation before day 20 was verified in 3/9 cows. Rate of growth of the last dominant follicle was 1.3mm/day in 2/9 cows and less in the remaining. Follicular cysts, poorly luteinized CL and endometries were diagnosed in 2/9, 2/9 and 1/9 cows respectively. In summary, alterations in ovarian and uterine functions were caused by presence and operation of uterine catheters and such alterations were incompatible with maintenance of pregnancy. In conclusion, the surgical approach tested was not adequate for studyng the uterine microenvironment of pregnant cows

Um condicionador de ar para biotérios foi montado com módulos termoelétricos de efeito Peltier. Para troca térmica, foram testados: 1. dissipação externa a ar, com &delta;t de 14°C, rendimento de 16,46%, consumo de 1212 W/h e, 2. dissipação externa água, com &delta;t de 21°C, rendimento de 46,02%, consumo de 524 W/h. A simulação matemática de operação, com mistura de ar não condicionado, mostrou que o sistema pode servir, na dissipação a ar, a aproximadamente 91 microisoladores padrão rato e a aproximadamente 137, na dissipação a água. Quando comparado com um sistema de compressão de freon, o termoelétrico mostrou economia de 26% na implantação e 38% no consumo elétrico por BTU gerado. O sistema termoelétrico mostrou ainda, precisão de &plusmn; 0,1°C, nas temperaturas experimentais, o que é impossível num sistema de freon. Para os testes em animais foram empregados Ratos wistar, mantidos individualmente, em gaiolas metabólicas de arame, sem abrigo, em sistema microambiental, sob fluxo direto de ar a 0,6 m/s, nas temperaturas de 22°, 24°, 26°, 28° e 30°C (E I, E II, E III, E IV e E V). A ingestão de ração e o ganho de peso foram comparados ao final de 5 dias (ANOVA; Tukey-Kramer). No total, 7 grupos de 15 animais cada foram comparados. Para a faixa de 22°C foram utilizados 3 grupos, sendo um grupo experimental e dois grupos controle (CI e C II). Um deles foi mantido em condições ambientais semelhantes a biotérios convencionais sob ventilação geral diluidora (VGD) - C I. O outro grupo controle (C II) foi mantido no interior do equipamento de ventilação microambiental, porém, sem o direcionamento de ar, simulando a VGD. Os resultados obtidos demonstraram claramente que animais mantidos sob ventilação microambiental direta a 26°, 28° e 30° (E III, E IV e E V) apresentaram o mesmo ganho de massa corpórea que animais do grupo C I (22 &plusmn; 2°C). Os grupos E I e E II apresentaram menor ganho de massa corpórea quando comparados a C I (p<0,001 em ambas comparações). O ganho de peso de todos os grupos experimentais apresentou diferença estatística, quando comparado ao C II, exceto o grupo E V que obteve índice de ganho de peso equivalente a C II. A ingestão de ração de todos os grupos se manteve praticamente constante. O grupo E V apresentou uma redução na ingestão de ração quando comparado aos grupos C I, E I e E II (p<0,01; p<0,01; p<0,001 respectivamente). O grupo E III ingeriu menos ração que os grupos C I (p<0,05) e E II (p<0,05). / An air-conditioner for animal facility was assembled with Peltier effect thermoelectric modules. For external exchanger, had been tested: 1. external air dissipation: &delta;t = 14°C; 16,46% of efficiency; 1212 W/h of power consumption and, 2. external water dissipation: &delta;t = 21°C; 46,02% of efficiency; 524 W/h of power consumption. A mathematical simulation of operation, with not conditional air mixture, showed that the system can supply, with air dissipation, to &asymp; 91 microisolator rat cages and to &asymp; 137, with water dissipation. When compared with a freon system, the thermoelectric system shows economy of 26% in implantation and 38% in the electric consumption by generated BTU. The thermoelectric system showed too, a precision of ± 0,1°C, at experimental temperatures, what is impossible in a freon system. For animal tests, Wistar rats had been kept individually, in metabolic wire cages, without shelter, in microenvironmental system, under direct air flow at 0,6 m/s, under temperatures of 22°, 24°, 26°, 28° and 30° C (E I, E II, E III, E IV and E V). The food ingestion and the weight gain had been compared in the end of 5 days (ANOVA; Tukey-Kramer). In the total, 7 groups, 15 animals each, had been compared. For the 22°C temperature, had been used 3 groups, one experimental and two controls (C I e C II). One of them was kept in similar ambient of conventional laboratory animal rooms conditions (general diluitory ventilation, GDV) - C I. The other control group (C II) was kept in the interior of the equipment of microenvironmental ventilation, however, without the direct air flow, simulating the GDV. The gotten results demonstrate clearly that animal kept under direct microenvironmental ventilation at 26°, 28° and 30°C (E III, E IV and E V) have the same gain of corporal mass that C I group (22 &plusmn; 2°C). The E I and E II had less corporal mass gain when compared to C I (p<0,001 for the two comparisons). The weight gain for all the experimental groups, when compared to C II, presents statistical differences, except E V group, that was equal to C II. The food ingestion of all the groups was constant. The E V group presented a reduction in the food ingestion when compared with the groups C I , E I and E II (p<0,01; p<0,01; p<0,001 respectively). The E III group ingested less ration than C I (p<0,05) and E II (p<0,05) groups.

Em bovinos, a mortalidade embrionária associada a falhas no processo de reconhecimento materno da prenhez atinge 30 a 40%. O sucesso da prenhez, depende de uma apropriada interação bioquímica entre o endométrio materno e o concepto. O objetivo dessa tese foi desenvolver uma técnica cirúrgica para monitorar o microambiente uterino de vacas cíclicas e prenhez nos dias 14 a 20 após o estro. Como objetivos específicos foram verificados se a implantação e a presença dos cateteres uterinos afetariam (1) a manutenção da prenhez, (2) a função luteal e (3) o desenvolvimento folicular. Em vacas holandesas, cíclicas e não lactantes, foram implantadas cateteres de silicone em cada corno uterino no segundo dia após o estro (fase preparatória). No dia 15 pós-estro os animais receberam uma injeção de D-clorprostenol e a ovulação foi confirmada por ultrasonografia transretal (US; dia experimental 1). No dia experimental 7, as vacas (n=6) receberam ou não (n=3) transferência de embriões via transcervical no corno uterino ipisilateral ao ovário contendo o corpo lúteo (CL). Nos dias experimentais 14, 16, 18 e 20, estruturas ovarianas foram avaliadas por US, e cada corno uterino foi lavado através dos cateteres implantados no lúmen uterino (três sessões de 6 ml cada). Amostras de sangue foram coletadas nos dias 1 a 20 da fase experimental e concentração de progesterona (P4) foi mensurada por radioimunoensaio. As vacas foram abatidas no dia experimental 20 e a prenhez diagnosticada por visualização macroscópica do concepto após a dissecação do útero. A taxa de presença do concepto no dia 20 experimental foi 0%. No dia experimental 7, um CL e um folículo grande (9 a 17 mm) estavam presentes nos ovários das vacas. A taxa de aumento da concentração de P4 entre os dias 1 a 5 foi de 0 ng/mL/dia em 7/9 vacas. Luteólise ocorreu antes do dia 15 em 3/9 vacas, entre os dias 16 e 20 foi 3/9, e após o dia 20 em 2/9 vacas. Não houve aumento de P4 na fase luteal em uma vaca. Foi verificado ovulação antes do dia 20 em 3/9 vacas. A taxa de aumento do último folículo dominante foi de 1,3mm/dia em 2/9 vacas e menor nos animais restantes. Cistos foliculares, CL sub-luteinizado e endometrite foram diagnosticados em 2/9, 2/9 e 1/9 vacas, respectivamente. Foi possível concluir que as alterações nas funções ovarianas e uterinas foram causadas pela presença e implantação dos cateteres e essas alterações foram incompatíveis com a manutenção da prenhez. A abordagem cirúrgica testada não foi adequada para estudar o microambiente uterino de vacas prenhez / In cattle, embryonic mortality associated with failure in the process of maternal recognition of pregnancy reaches 30 to 40%. Successful pregnancies depend on appropriate biochemical interactions between the maternal endometrium and conceptus. Overall objective was to develop a surgical technique to probe the uterine microenvironment of cyclic and pregnant cows days 14 to 20 post- estrus. Specific objectives were to verify whether presence and operation of uterine catheters would affect (1) maintenance of pregnancy, (2) luteal function and (3) follicular growth. Non-lactating, cyclic, Holstein cows were fitted with a silicone catheter in each uterine horn on day 2 after estrus. On day 15 they received an injection of D-cloprostenol and ovulations were confirmed by transrectal ultrasonography (US; experimental day 1). On experimental day 7, cows received (n=6) or not (n=3) embryos by trans-cervical transfer to the uterine horn ipsilateral to ovary containing the corpus luteum (CL). On experimental days 14, 16, 18 and 20, ovarian strutures were observed by US and each uterine horn was washed through the catheter (three sessions of 6 ml each). Blood samples were collected from experimental days 1 to 20 and progesterone (P4) concentrations were measured by radioimmnoassay. Cows were slaughtered on experimental day 20 and pregnancies were diagnosed by macroscopic visualization of a conceptus after dissection of uterus. Conception rate at day 20 was 0%. On experimental day 7, both a CL and a large follicle (9 to 17mm) were present in ovaries of all cows. Rate of increase of P4 concentrations from days 1 to 5 was 0ng/ml/day in 7/9 cows. Luteolysis occurred before day 15 in 3/9 cows, between days 16 and 20 in 3/9 cows and after day 20 on 2/9 cows. No luteal phase rise in P4 was noticed for one cow. Ovulation before day 20 was verified in 3/9 cows. Rate of growth of the last dominant follicle was 1.3mm/day in 2/9 cows and less in the remaining. Follicular cysts, poorly luteinized CL and endometries were diagnosed in 2/9, 2/9 and 1/9 cows respectively. In summary, alterations in ovarian and uterine functions were caused by presence and operation of uterine catheters and such alterations were incompatible with maintenance of pregnancy. In conclusion, the surgical approach tested was not adequate for studyng the uterine microenvironment of pregnant cows

Cancer metastasis is the critical event leading to 90% of cancer related death. Although significant improvement in our understanding on cancer metastasis has been made through years of research, the fundamental mechanism behind this process is still not fully elucidated. For cancer researchers, the “gold standard” for metastasis studies has traditionally been the use of tissue culture and mouse models. Tissue culture offers the simplest system and ease of control but is not able to recapitulate many of the features found in an in vivo tumor microenvironment. On the other hand, mouse model systems offer the most sophisticated and physiologically relevant platforms for studying cancer. However, the lack of control over the in vivo environment in these mouse models and inherent discrepancies from human physiology make results from these models difficult to be translated to clinical trials. The advancement in microfabrication techniques and cancer models developed based on these techniques has shown potential in addressing the gap between in vitro tissue culture and mouse models. Microscopic tumor microenvironments could be built in these in vitro systems to study behavior of human cancer cells. However, the expertise involved in and extra instrumentation needed for implementing these systems have prevented their widespread use by general cancer researchers. In this dissertation, we developed two simple microfabricated systems and demonstrated their application in two aspects of cancer research. The first system is a microfabricated cell patterning stencil, where paracrine signaling can be established and its impact can be measured based on cell migration. Using this tool, we investigated the interaction between melanoma and microenvironmental cells from their common metastasis target organ. Through these simple patterning techniques, we observed significant effects that a given microenvironmental cell line had on the two different melanoma lines, as well as how melanoma affected different microenvironmental cell lines. The second system, a microfluidic device, is able to present individual soluble factors to cancer cells in order to test the response of cancer cells to these physiologically relevant factors. Through this stand-alone system, we found that breast cancer metastasis is influenced by the protein molecules secreted by themselves as well as the local glucose level. Through these findings we believe that our microfabricated systems can benefit the general cancer research community in which a complicated problem can be broken down into manageable pieces and studied on a simple platform in a controlled way. Observation made through these systems can inspire general cancer researchers to form new hypotheses and eventually lead to new findings. / 2017-02-17T00:00:00Z

Chronic Lymphocytic Leukemia (CLL) is defined by the accumulation of clonally expanded CD5+ and CD19+ B lymphocytes in blood and secondary lymphoid organs with impaired apoptotic mechanisms. CLL represents one third of all leukemia cases with an average age of 72 years at diagnosis making it the most common adult leukemia. The Eµ-Tcl1 mouse serves as an excellent model to study the development of CLL as they progress to a CLL like disease by 9-14 months of age, due to overexpression of an oncogene, T cell Leukemia 1(Tcl1), specifically in B cells through the Ig VH promoter and Eµ enhancer (Bichi et al. PNAS. 2002). In an adoptive transfer model, intravenous or intraperitoneal injection of primary CD5+CD19+ CLL cells from the Eµ-Tcl1 CLL mouse into recipient syngeneic mice leads to the development of a CLL like disease within 3-8 weeks of transfer. We have characterized the growth of CLL cells in these mice by periodic submandibular bleeding, spleen ultrasonography and flow cytometry. We find that Eµ-Tcl1 CLL cells express more Prostate apoptosis response-4 protein (Par-4), a known pro-apoptotic tumor suppressor protein, than normal B-1 or B-2 cells in mice. Par-4 is silenced by promoter methylation in more than 30% of all cancers and has been shown to be secreted and to induce apoptosis selectively in various types of cancer cells but not in normal cells. We found that CLL cells have constitutively active B-cell receptor signaling (BCR) and that inhibition of BCR signaling with FDA approved drugs causes a decrease in Par-4 protein, mRNA levels, and an increase in apoptosis. In particular, activities of Src family kinases, spleen tyrosine kinase and Bruton’s tyrosine kinase are required for Par-4 expression in CLL cells, suggesting a novel regulation of Par-4 through BCR signaling in both Eµ-Tcl1 CLL cells and primary human CLL samples. Consistent with this, lenti-viral shRNA mediated knockdown of Lyn kinase leads to a decrease in Par-4 expression in MEC-1 cells, a human CLL derived cell line. Igα (CD79a) silencing in primary human CLL cells also results in down regulation of Par-4 expression. Additionally, we knocked down expression of Par-4 in MEC-1 cells which resulted in a decrease in cell growth that could be attributed to an increase in p21 expression and a reduction in the G1/S cell cycle transition. We have also observed this phenomenon by crossing mice deficient in Par-4 with the Eµ-Tcl1 mouse where lack of Par-4 delays CLL growth in the mouse significantly (time to euthanization due to poor body condition - Eµ-Tcl1: 8.9mo vs Par4-/-EµTcl1: 11.97 mo, p = 0.0472) and splenic B-CLL cells from these mice also have increased expression of p21. Since mice in this cohort are whole body knockout for Par-4, the difference in survival times between the Par-4 +ve and Par-4 –ve EµTcl1 mice could be due to the influence of Par-4 on CLL cells as well as the effect of Par-4 secreted by the CLL cells on the microenvironment. There could be other potential roles for Par-4 in the context of CLL which are under further investigation. We have also investigated the site of CLL growth in mouse models to determine that the spleen is the primary organ to accumulate the CLL tumor burden. We have found that splenectomy significantly delays the development of CLL in the primary Eμ-Tcl1 mouse model and prevents growth and development in the adoptive transfer model. Interestingly, splenectomy did not delay CLL development as significantly in animals deficient for Par-4 compared to C57BL/6 wild type mice. Par-4 appears to regulate a specific microenvironment required for CLL growth. Current studies are investigating the role of Par-4 in the microenvironment and the cell types that are critical for CLL growth within the splenic niche.

The potential of a soil to immobilize heavy metal ions is dependent on the presence of adsorption sites, and the stability of metal species over the range of geochemical conditions present in the soil over time. Lead (Pb) is a cumulative toxin that is enriched in much of the urban pedosphere due to historical use of Pb-based paint and Pb-amended gasoline. Because in-situ remediation of Pb is possible if the bioavailable fraction can be rendered inert, understanding Pb-sorbent interactions is necessary to accurately and efficiently alter Pb speciation in soils. The objectives of this study are to 1) determine efficient ways to predict Pb behavior at the field scale, and 2) characterize microscale controls on Pb speciation. A combination of geospatial and analytical tools has been used across a variety of spatial scales to provide the first multiscale analysis of microenvironment impact on Pb speciation in soils. This research investigated Pb distribution at the field scale (in Burlington, VT), and mobility at the microscale. The field-scale study has shown that the relationship between total Pb and bioaccessible Pb is not linear, in stark contrast to the existing conceptual model of this relationship. It was determined that the disproportional influence of fine-fraction Pb in low total-Pb soils results in elevated bioavailability. Microscale investigations determined that there is a positive correlation between the density of reactive microenvironments and the release of Pb from contaminated soil, and that altered distributions of microenvironments significantly alters the rate of Pb release. This research identifies specific mechanisms controlling Pb behavior in soils at both the field and the microscale, which can be used to inform improvements to implementation of remediation.

Les syndromes myélodysplasiques (MDS) sont un groupe de pathologies myéloïdes caractérisées par une hématopoïèse inefficace. Le rôle du microenvironnement médullaire (MM) dans l’histoire naturelle de ces pathologies reste incertain. Des anomalies du MM ont été décrites au cours des myélodysplasies et des modèles murins récemment publiés font penser qu’une altération du MM pourrait jouer un rôle dans le déclenchement et/ou l’évolution de ces maladies.Nous avons tenté de développer un modèle in vivo récapitulant l’histoire naturelle des myélodysplasies par des xénogreffes chez des souris NSG et NSG-S. Le faible taux de prise de greffe nous a amenés à développer un modèle in vitro de co-culture en 2D. Ce modèle est une bonne alternative pour les études de nouvelles stratégies thérapeutiques pour les patients atteints de myélodysplasies.Au cours de ce travail, nous avons également réalisé une étude systématique du stroma médullaire de patients atteints de syndromes myélodysplasiques dans le but d’identifier les anomalies fonctionnelles et moléculaires des cellules souches mésenchymateuses (CSMs), cellules centrales du MM pour leur interaction avec les cellules souches hématopoïétiques (CSHs).Les CSMs de MDS ont une clonogénécité diminuée. Nous n’avons pas observé de modification significative de leurs capacités de différenciation en ostéoblastes, adipocytes et chondrocytes ni dans leur capacité à supporter une hématopoïèse normale. Les CSMs de MDS présentent des modifications au niveau épigénétique et transcriptionnel pouvant expliquer l’altération des relations observées grâce à de l’imagerie enregistrée entre les CSMs de MDS et les CSHs dans un modèle de co-culture en 3D.Ces résultats montrent que les CSMs de MDS ont des modifications fonctionnelles et moléculaires et que ces anomalies perturbent leur relation avec les CSHs. / Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal myeloid pathologies characterized by an impaired hematopoiesis. The role of the bone marrow microenvironment (BMM) remains unclear in the natural history of these diseases. Abnormalities of the BMM have been observed in myelodysplasia and a recent published murine model implies that alterations of the BMM could play a role in the trigger/progression of these diseases.Firstly, we tried to develop an in vivo model of MDS in NSG and NSG-S mice. The low rate of engraftment pushed us to develop a 2D co-culture model in vitro. This model is a good alternative to test new therapeutic strategies for MDS patients.In this study, we analysed mesenchymal stromal cells (MSCs) from the bone marrow of pretreated MDS patients in order to identify the functional and molecular abnormalities in those cells of the BMM, central for their interactions with the hematopoietic stem cells (HSCs).MDS MSCs have an impaired clonogenic capacity. We didn’t observed modifications of their differentiation toward osteogenic, adipogenic and chondrogenic pathways and capacity to support of a normal hematopoiesis. MDS MSCs display epigenetic and transcriptomic modifications that could explain the alteration of the relationships between these cells and HSCs observed in imagery in a 3D co-culture model.These results showed that MDS MSCs have functional and molecular abnormalities and that these alterations could impair their relationship with HSCs.

C3 glomerulopathy (C3G) encompasses a group of severe renal diseases characterized by “dominant C3” deposition in the renal glomerulus. Patients typically present as nephritic nephrotics, with hematuria, hypertension, heavy proteinuria and edema. Within ten years of diagnosis, 50% of affected patients progress to end-stage renal disease and require dialysis or renal transplantation. No treatment is available to halt disease progression and thus both disease recurrence and allograft loss are common after transplantation. Genetic studies of C3G have firmly implicated dysregulation of the alternative pathway (AP) of complement in disease pathogenesis. In addition to genetic factors, acquired factors like autoantibodies can also exaggerate AP activity in the circulation to cause C3G. Although AP dysregulation in the circulation (i.e. fluid-phase dysregulation) has been well studied in these patients, AP activity in the glomerular microenvironment is not well understood. In this body of work, we used MaxGel, an ex-vivo surrogate for the glomerular extracellular matrix, to study AP activity and regulation. We showed that C3 convertase can be assembled on MaxGel and elucidated the dynamics of its formation and decay in the presence of complement regulators. We confirm that on MaxGel factor H (fH) inhibits C3 convertase formation and accelerates its decay, while properdin has a stabilizing effect. We also show that the complement factor H-related proteins (FHRs) are vital to the regulation of AP activity. Consistent with our MaxGel data, CFHR gene-fusion events have been reported as genetic drivers of disease in a few familial cases of C3G. One such familial case in which we identified and characterized the rearrangement event results from a novel CFHR5-CFHR2 fusion gene. The fusion gene is translated into a circulating FHR-5/-2 protein that consists of the first two SCRs of FHR-5 followed by all four SCRs of FHR-2. The structural repetition of SCR1-2 followed by another SCR1-2 motif facilitates the formation of complex FHR-1, FHR-2 and FHR-5 multimers, which have enhanced affinity for C3b and by out-competing fH, lead to impaired C3 convertase regulation in the glomerular microenvironment. Finally, we tested gene therapy as a tool to rescue the disease phenotype and restore fluid-phase AP complement control in a mouse model of C3G (Cfh-/-/huCR1-Tg mice). Using the piggyBac transposon system, we introduced a construct derived from complement regulator 1 (CR1) into Cfh-/-/huCR1-Tg mice. Delivery of sCR1-AC via hydrodynamic tail vein injection provided constitutive circulatory expression of sCR1-AC, and in animals followed for 6 months, we found that long-term expression of this complement regulator rescued the renal phenotype. These results suggest that sCR1 may be a potential therapy for patients with this disease.

No description available.