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Ascorbate (Asc) is a key antioxidant in preventing cardiovascular dysfunction during diseases exacerbated by altered shear stress. According to the literature endothelial responses to hypotonic shock share some characteristics with those induced by shear stress. Thus to study the physiological responses of endothelium to shear stress, the characterization of the Asc release by pig coronary artery endothelial cells in response to hypotonic shock was performed. The pig coronary artery endothelial cells that had been loaded with ^14C Asc and ^3H deoxyglucose, were exposed to buffers of varying osmolality for different time periods and the release of ^14C Asc and ^3H deoxyglucose was examined. Based on various parameters like relative release of ^14C Asc and ^3H deoxyglucose, their rate of release and protein loss, it was decided to use buffer of .67 percent osmolality for 2 min for these characterization studies. The Asc release was authentic and not a result of membrane damage. The hypotonic shock induced Asc release was not due to endogenously released ATP. The inhibition of ATP induced release by anion channel inhibitors niflumic acid and NPPB was complete but only partial in case of hypotonic shock induced release. The release was not inhibited under nominally Ca^2+ free conditions. Additive release by hypotonic shock and ATP or hypotonic shock and Ca^2+ ionophore A23187 suggests that there are two independent Asc release pathways. Asc release by two different mechanisms may help endothelial cells deal with stressful conditions efficiently and preserve endothelial function. / Thesis / Master of Science (MS)

El éxito de la fecundación humana depende, entre otros eventos moleculares, de la capacidad de los espermatozoides para llevar a cabo de forma adecuada la capacitación. Este proceso implica una serie de cambios bioquímicos en los espermatozoides para favorecer su interacción con el gameto femenino. Aunque es posible capacitar las células in vitro, el tiempo óptimo para que un espermatozoide complete la capacitación en estas condiciones sigue siendo objeto de debate debido a la falta de biomarcadores de capacitación adecuados. Los estudios en esta área, se han centrado en aquellos receptores espermáticos implicados en la interacción entre gametos. En particular, el complejo molecular formado por la proteína de choque térmico A2 (HSPA2; del inglés heat shock protein A2), la molécula de adhesión a hialuronidasa 1 (SPAM1; del inglés sperm adhesion molecule 1) y la proteína arilsulfatasa A (ARSA; del inglés arylsulfatase A), ha sido estudiado por varios grupos de investigación debido a su participación en el reconocimiento del ovocito por parte del espermatozoide. Los estudios más relevantes sobre la ubicación de este complejo se basan en la evidencia de la colocalización de estas proteínas en la región periacrosomal de la cabeza espermática. Sin embargo,Esta premisa es controvertida, ya que otros autores han encontrado una asociación entre diferentes áreas de distribución de HSPA2 en la cabeza del espermatozoide y la fertilidad. A pesar del importante papel que desempeña este complejo proteico durante la unión del espermatozoide a la zona pelúcida del ovocito (ZP), aún no se ha ilustrado el grado de dependencia del tiempo de capacitación sobre la presencia y distribución de una topografía específica en la superficie espermática de estas proteínas. Con esta premisa, en la presente tesis evaluamos la influencia del tiempo de capacitación in vitro en la localización y distribución de HSPA2 y ARSA en la cabeza de espermatozoides humanos. De esta manera, y mediante microscopía de fluorescencia, se evaluó la presencia de HSPA2 y ARSA en donantes normozoospérmicos2 tanto antes como tras la capacitación in vitro durante una y cuatro horas. Además, se utilizó la microscopía electrónica de campo de alta resolución (FE-SEM; microscopía electrónica de barrido de emisión de campo; del inglés field emission scanning electron microscopy) para cuantificar la densidad de ARSA y la localización específica de esta proteína en los diferentes dominios de la membrana espermática antes y después de la capacitación in vitro durante una y cuatro horas. Con respecto al porcentaje de células positivas para HSPA2, no se observaron diferencias significativas entre las poblaciones analizadas antes y después de una hora de capacitación. No obstante, observamos un porcentaje significativamente mayor de células marcadas con HSPA2 tras cuatro horas de capacitación in vitro. A pesar de que no se pudo determinar un patrón de distribución de HSPA2 predominante en las células que fueron positivas antes de la capacitación, el patrón de distribución mayoritario después de la capacitación fue de fluorescencia en la banda ecuatorial y el acrosoma. Al estudiar la distribución de ARSA se observó un aumento significativo en el porcentaje de células positivas para esta proteína tras la capacitación, pero sin diferencias entre una y cuatro horas de incubación. Al igual que ocurría con HSPA2, el análisis mediante microscopía de fluorescencia no mostró un patrón mayoritario de distribución de ARSA en la subpoblación espermática previa a la capacitación, mientras que, tras este proceso las células presentaron de manera predominante un marcaje intenso en la región acrosomal. Por otra parte, el análisis mediante microscopía electrónica de barrido de emisión de campo mostró una agregación de ARSA en la región periacrosomal tras la capacitación. Nuestros resultados apuntan que el complejo formado por HSPA2, ARSA y SPAM1 requiere más de una hora de capacitación in vitro para distribuirse correctamente en la cabeza espermática. Además, el presente estudio proporciona evidencias sólidas de la utilidad de HSPA2 y ARSA como biomarcadores de capacitación, sugiriendo su uso como biomarcadores suplementarios al clásico análisis seminal previo a una técnica de reproducción artificial. / Este trabajo de investigación ha sido subvencionado por la Cátedra Human Fertility de la Universidad de Alicante y los proyectos de I+D+i ViGrob-186 y UAIND17-03.

High temperatures are a significant biological stressor for mammals, which they may adapt to through behavioral changes, physiological plasticity, and via genetic adaptation. Savanna monkeys (genus Chlorocebus) have a wide climatic range in Africa south of the Sahara, making them a good model species for understanding adaptations to heat stress in primates. Savanna monkeys have been observed to behaviorally mitigate high temperatures, and genetic signs of selection in response to climate have also been found (specifically in relation to cold). In this study, I investigate whether there is genetic variation and evidence for selection related to function in a heat shock protein gene (HSPA1L) in 73 wild savanna monkeys ranging from equatorial Africa to the southern coast of South Africa. Given the important role of heat shock proteins in buffering heat stress, I hypothesized that genetic variation would be associated with maximum summer temperatures, as those are most likely to be warm enough to induce a heat shock response. I found 45 single nucleotide polymorphisms (SNPs) outside of Hardy-Weinberg Equilibrium, and 10 SNPs with significant integrated haplotype scores, only one of which was in a protein coding region (17:40210341; piHS = 2.20). Using phylogenetic least squares modeling I found that maximum temperature of the warmest month was strongly but not significantly associated with the frequency of a derived allele nested within a regulatory region for HSPA1L (17:40207386; piHS = 2.57; b = 0.044, p = 0.061) presumably experiencing selection. I discuss implications of these results for heat tolerance in primates and resilience to climate change.

Most proteins must fold into native three-dimensional structures to be functional. But, newly synthesized proteins are at high risk of misfolding and aggregating in the cell. Stress, disease or mutations can also cause protein aggregation. A cyanobacterial small heat shock protein, Hsp16.6, can act as a chaperone to prevent irreversible protein aggregation during heat stress. This thesis is focused on the properties of proteins that were associated with Hsp16.6 during heat stress, and which therefore may be “substrates” of Hsp16.6. Bioinformatics were used to determine if Hsp16.6 preferentially binds to proteins with certain properties, and biochemical studies were performed to investigate how the substrates actually behave with Hsp16.6 during heat stress. It was found that Hsp16.6 preferentially binds to proteins with higher molecular weight, higher acidity, higher percentage of charged residues (especially negatively charged residues), and a lower percentage of hydrophobic residues compared to all proteins encoded by the Synechocystis genome. Proteins bound to Hsp16.6 were also slightly enriched in VQL motifs. The potential substrate fructose bisphosphate aldolase class II (FBA) was expressed in E.coli and purified. FBA could be protected by Hsp16.6 from aggregation through forming a complex with Hsp16.6 during heat stress in vitro, consistent with it being a substrate of Hsp16.6. Another potential substrate, elongation factor G1 (EF-G1) was also expressed in E.coli and purified. EF-G1 did not form insoluble aggregates even at 47°C, but circular dichroism spectroscopy revealed the secondary structure has melted at this temperature, and the protein eluted earlier than unheated protein on size exclusion chromatography. Thus, EF-G1 appears heat sensitive, and may also be an in vivo substrate of Hsp16.6. Lastly, in vivo study studies were performed to determine the amount of FBA and EF-G1 in Synechocystis cells. Both proteins are abundant, with FBA levels (around 2% of total cell protein) being about twice that of EF-G1. Further in vivo experiments will be needed to confirm that FBA and EF-G1 are substrates of Hsp16.6.

Type IV pili (T4P) systems are widely utilized among bacteria to power and direct surface motility. The production and secretion of a viscous polysaccharide to provide friction and resistance to the extended pilus structure is seen in several species of cyanobacteria including Nostoc punctiforme. The complex coregulation of polysaccharide secretion and T4P motor activity is not fully understood, although studies indicate a consistent relationship between functional motility and intact pathways of polysaccharide secretion and pilus extension in cyanobacteria. Using a combination of protein-protein interaction analysis, cytological studies, and comparative genomics this study proposes a theoretical mechanism for T4P motor influenced regulation of hormogonium polysaccharide secretion by a heat-shock protein (HSP) DnaK-type chaperone system in N. punctiforme. The results of this study indicate a tripartite HSP system consisting of DnaK1, DnaJ3, and coregulator GrpE is influenced by the activation of certain motor proteins in the T4P complex and are required for the production and secretion of hormogonium polysaccharide. Conservation of this system in Synechocystis sp. also implies a potential system that is conserved among all motile cyanobacteria for regulation of T4P.

This research produced a new class of skin friction gages that measures wall shear even in shock environments. One test specimen separately measured wall shear and variable-pressure induced moment. Through the investigation of available computational modeling methods, techniques for accurately predicting gage physical responses were developed. The culmination of these model combinations was a design optimization procedure. This procedure was applied to three disparate test conditions: 1) short-duration, high-enthalpy testing, 2) blow-down testing, and 3) flight testing. The resulting optimized gage designs were virtually tested against each set of nominal load conditions. The finalized designs each successfully met their respective test condition constraints while maximizing strain output due to wall shear. These gages limit sources of apparent strain: inertia, temperature gradient, and uniform pressure. A unique use of bellows provided a protective shroud for surface strain gages. Oil fill provided thermal and dynamic damping while eliminating uniform pressure as a source of output voltage. Two Wheatstone bridge configurations were developed to minimize temperature effects first from temperature gradient and then from spatially varying heat flux induced gradient. An inertia limiting technique was developed that parametrically investigated mass and center of gravity impact on strain output. Multiple disciplinary computational simulations of thermal, dynamic, shear, moment, inertia, and instrumentation interaction were developed. Examinations of instrumentation error, settling time, filtering, multiple input dynamic response, and strain gage placement to avoid thermal gradient were conducted. Detailed mechanical drawings for several gages were produced for fabrication and future testing. / Ph. D.

A weak shock theory is developed which allows for dense gas effects when the fundamental derivative of gas dynarnics, Γ , becomes small and possibly negative. The nonclassical behavior in these negative Γ regions has potential applications in turbomachinery design. The weak shock development results in a Burgers equation which is then solved numerically using the well-known MacCormack scheme. The results include the demonstration of many non-classical results such as expansion shocks, compression fans, shock-splitting and shock-fan combinations. Results are shown which could help improve turbine efficiency. / M.S.

Turbine aerodynamic designers are currently focusing on unsteady passage flow to increase turbine performance. In particular, for high pressure turbine stages the effects of wakes and shocks shed from an upstream blade row on the downstream blade row need to be understood. Also, experimental data is needed for comparison with unsteady three-dimensional turbine stage calculations. Previous simulations of the unsteady shock/wake inlet flow field for a turbine rotor or stator used a rotating disk with radial bars upstream of a linear cascade. An alternate method of shock generation is developed here using a capped shock tube with multiple outlets to get a traveling system of three shock waves. Different lengths of tubing are used to get time delays between the shocks, which are then introduced at the top of a linear cascade of turbine blades and travel downwards (tangentially) along the leading edge. Advantages of this method include the absence of wakes and excellent two-dimensionality of the inlet shock waves. The period of the incoming shocks is easily adjustable to simulate different Strouhal numbers. Unsteady measurements of upstream total pressure, blade static pressures, and uncorrected downstream total pressure are made for a transonic mean flow with introduction of traveling shocks at M=1.3. An analytical solution (Bach and Lee, 1970) for the decay of cylindrical shock waves is used to estimate the behavior of flow variables other than pressure at the cascade inlet. The unsteady total pressure loss of the blade passage and the unsteady blade forces are measured with one shock passing and with three shocks passing at periods of 0.055 and 0.200 milliseconds. Loss is estimated as the normalized difference in unsteady total pressures and blade forces are integrated from seventeen unsteady surface pressure measurements. The Strouhal number for the 0.200 msec case is 2.9, which is typical of a high-pressure turbine nozzle or rotor. Periodic behavior in blade force and loss are observed for this case. Blade lift shows peak-to-peak variation of 6% and the estimated loss fluctuates by 100%. No change is observed in the average level of loss due to the incident shock waves. / Ph. D.