5 research outputs found

    Paper Session II-B - High Efficiency Hyperspectral Imager for the Terrestrial and Atmospheric Multispectral Explorer

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    The Terrestrial and Atmospheric MultiSpectral Explorer1 (TAMSE) is a Space Shuttle Small Self- Contained Payload “Get-Away Special” (GAS) project, led by Principal Investigator Rolando Branly, and including remote sensing and microgravity experiments from Florida Space Institute member schools. One of these experiments is the High-Efficiency HyperSpectral Imager (HEHSI). The HEHSI project will provide a low-cost spaceflight demonstration of a novel type of imaging spectrometer with exceptional light gathering ability. HEHSI is also a demonstration of what can be achieved in space with a modest budget: 15KfromtheFloridaSpaceGrantConsortium(FSGC)and 15K from the Florida Space Grant Consortium (FSGC) and 10K from the Florida Space Institute (FSI). Education and workforce development are important goals of the project, with all of the mechanical, electronics, and software design and testing being carried out by an interdisciplinary team of FSI students. These six students, who are about to graduate with bachelor’s degrees in engineering (three computer, one electrical, and two aerospace), have worked on the project and received course credit for two semesters. The matching funds from FSI support the involvement of the mentor for the HEHSI experiment, Glenn Sellar, who is also responsible for the optical design. Environmental testing (thermal and vibration) will be carried out by the students at KSC’s Physical Testing Laboratory, under a cooperative Space Act Agreement. As this instrument is the first remote sensing payload constructed in Florida (to the authors knowledge), it also serves as a seed for diversification of the space industry in Florida. An overview of the project is presented in this paper, including the science objectives, and the optical, mechanical, electrical, and software designs

    Immune activation in irritable bowel syndrome: can neuroimmune interactions explain symptoms?

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    Irritable bowel syndrome (IBS) is a functional disorder of the gastrointestinal (GI) tract characterized by pain or discomfort from the lower abdominal region, which is associated with altered bowel habit. Despite its prevalence, there is currently a lack of effective treatment options for patients. IBS has long been considered as a neurological condition resulting from alterations in the brain gut axis, but immunological alterations are increasingly reported in IBS patients, consistent with the hypothesis that there is a chronic, but low-grade, immune activation. Mediators released by immune cells act to either dampen or amplify the activity of GI nerves. Release of a number of these mediators correlates with symptoms of IBS, highlighting the importance of interactions between the immune and the nervous systems. Investigation of the role of microbiota in these interactions is in its early stages, but may provide many answers regarding the mechanisms underlying activation of the immune system in IBS. Identifying what the key changes in the GI immune system are in IBS and how these changes modulate viscerosensory nervous function is essential for the development of novel therapies for the underlying disorder.Patrick A. Hughes, Heddy Zola, Irmeli A. Penttila, L. Ashley Blackshaw, Jane M. Andrews, and Doreen Krumbiege

    De novo biosynthesis of sterols and fatty acids in the Trypanosoma brucei procyclic form:carbon source preferences and metabolic flux redistributions

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    Abstract De novo biosynthesis of lipids is essential for Trypanosoma brucei, a protist responsible for the sleeping sickness. Here, we demonstrate that the ketogenic carbon sources, threonine, acetate and glucose, are precursors for both fatty acid and sterol synthesis, while leucine only contributes to sterol production in the tsetse fly midgut stage of the parasite. Degradation of these carbon sources into lipids was investigated using a combination of reverse genetics and analysis of radio-labelled precursors incorporation into lipids. For instance, (i) deletion of the gene encoding isovaleryl-CoA dehydrogenase, involved in the leucine degradation pathway, abolished leucine incorporation into sterols, and (ii) RNAi-mediated down-regulation of the SCP2-thiolase gene expression abolished incorporation of the three ketogenic carbon sources into sterols. The SCP2-thiolase is part of a unidirectional two-step bridge between the fatty acid precursor, acetyl-CoA, and the precursor of the mevalonate pathway leading to sterol biosynthesis, 3-hydroxy-3-methylglutaryl-CoA. Metabolic flux through this bridge is increased either in the isovaleryl-CoA dehydrogenase null mutant or when the degradation of the ketogenic carbon sources is affected. We also observed a preference for fatty acids synthesis from ketogenic carbon sources, since blocking acetyl-CoA production from both glucose and threonine abolished acetate incorporation into sterols, while incorporation of acetate into fatty acids was increased. Interestingly, the growth of the isovaleryl-CoA dehydrogenase null mutant, but not that of the parental cells, is interrupted in the absence of ketogenic carbon sources, including lipids, which demonstrates the essential role of the mevalonate pathway. We concluded that procyclic trypanosomes have a strong preference for fatty acid versus sterol biosynthesis from ketogenic carbon sources, and as a consequence, that leucine is likely to be the main source, if not the only one, used by trypanosomes in the infected insect vector digestive tract to feed the mevalonate pathway

    Irritable bowel syndrome

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    Irritable bowel syndrome (IBS) is a functional gastrointestinal disease with a high population prevalence. The disorder can be debilitating in some patients, whereas others may have mild or moderate symptoms. The most important single risk factors are female sex, younger age and preceding gastrointestinal infections. Clinical symptoms of IBS include abdominal pain or discomfort, stool irregularities and bloating, as well as other somatic, visceral and psychiatric comorbidities. Currently, the diagnosis of IBS is based on symptoms and the exclusion of other organic diseases, and therapy includes drug treatment of the predominant symptoms, nutrition and psychotherapy. Although the underlying pathogenesis is far from understood, aetiological factors include increased epithelial hyperpermeability, dysbiosis, inflammation, visceral hypersensitivity, epigenetics and genetics, and altered brain-gut interactions. IBS considerably affects quality of life and imposes a profound burden on patients, physicians and the health-care system. The past decade has seen remarkable progress in our understanding of functional bowel disorders such as IBS that will be summarized in this Primer
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