15,209 research outputs found

    Exposure to the Dental Environment and Prevalence of Respiratory Illness in Dental Student Populations

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    Objective: To determine if the prevalence of respiratory disease among dental students and dental residents varies with their exposure to the clinical dental environment. Methods: A detailed questionnaire was administered to 817 students at 3 dental schools. The questionnaire sought information concerning demographic characteristics, school year, exposure to the dental environment and dental procedures, and history of respiratory disease. The data obtained were subjected to bivariate and multiple logistic regression analysis. Results: Respondents reported experiencing the following respiratory conditions during the previous year: asthma (26 cases), bronchitis (11 cases), chronic lung disease (6 cases), pneumonia (5 cases) and streptococcal pharyngitis (50 cases). Bivariate statistical analyses indicated no significant associations between the prevalence of any of the respiratory conditions and year in dental school, except for asthma, for which there was a significantly higher prevalence at 1 school compared to the other 2 schools. When all cases of respiratory disease were combined as a composite variable and subjected to multivariate logistic regression analysis controlling for age, sex, race, dental school, smoking history and alcohol consumption, no statistically significant association was observed between respiratory condition and year in dental school or exposure to the dental environment as a dental patient. Conclusion: No association was found between the prevalence of respiratory disease and a student\u27s year in dental school or previous exposure to the dental environment as a patient. These results suggest that exposure to the dental environment does not increase the risk for respiratory infection in healthy dental health care workers

    Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

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    Mitochondrial morphology is determined by a dynamic equilibrium between organelle fusion and fission, but the significance of these processes in vertebrates is unknown. The mitofusins, Mfn1 and Mfn2, have been shown to affect mitochondrial morphology when overexpressed. We find that mice deficient in either Mfn1 or Mfn2 die in midgestation. However, whereas Mfn2 mutant embryos have a specific and severe disruption of the placental trophoblast giant cell layer, Mfn1-deficient giant cells are normal. Embryonic fibroblasts lacking Mfn1 or Mfn2 display distinct types of fragmented mitochondria, a phenotype we determine to be due to a severe reduction in mitochondrial fusion. Moreover, we find that Mfn1 and Mfn2 form homotypic and heterotypic complexes and show, by rescue of mutant cells, that the homotypic complexes are functional for fusion. We conclude that Mfn1 and Mfn2 have both redundant and distinct functions and act in three separate molecular complexes to promote mitochondrial fusion. Strikingly, a subset of mitochondria in mutant cells lose membrane potential. Therefore, mitochondrial fusion is essential for embryonic development, and by enabling cooperation between mitochondria, has protective effects on the mitochondrial population

    The fundamental drivers of electrochemical barriers

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    Reaction barriers dictate the rates of elementary reactions, and therefore are crucial to understanding electrochemical kinetics. Since these reactions tend to occur at heterogeneous surfaces, principles from catalysis can be expected to apply. Here, we use electronically grand-canonical calculations on a model system of the proton-deposition reaction on a range of metal surfaces to explore the extent to which these principles hold. First, we show that while reaction barriers are functions of potential, unlike endstates they tend to exhibit a nonlinear dependence, and this nonlinearity can be traced to differences in the electron transfer at the reaction barrier. We show that along a reaction path, this same electron-transfer difference forces the barrier to move earlier for downhill reactions, enforcing and explaining the Hammond-Leffler postulate for electrochemical reactions, as well as explaining the curvature in the Marcus-like relations. We further examine trends in barrier energies, at equivalent driving forces, for this reaction across metals. We find that the barrier energy correlates weakly to the hydrogen binding energy and the d-band center, but instead correlates strongly with the charge presented at the metal surface -- which is a direct consequence of the native work function of the material. This suggests that the energetics of the barrier are driven more strongly by the electrostatic, rather than the covalent, nature of the metal-adsorbate interaction, and suggests electrochemical barriers may have an independent driving force from electrochemical adsorbates

    Efficient cytosolic delivery of molecular beacon conjugates and flow cytometric analysis of target RNA

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    Fluorescent microscopy experiments show that when 2′-O-methyl-modified molecular beacons (MBs) are introduced into NIH/3T3 cells, they elicit a nonspecific signal in the nucleus. This false-positive signal can be avoided by conjugating MBs to macromolecules (e.g. NeutrAvidin) that prevent nuclear sequestration, but the presence of a macromolecule makes efficient cytosolic delivery of these probes challenging. In this study, we explored various methods including TAT peptide, Streptolysin O and microporation for delivering NeutrAvidin-conjugates into the cytosol of living cells. Surprisingly, all of these strategies led to entrapment of the conjugates within lysosomes within 24 h. When the conjugates were pegylated, to help prevent intracellular recognition, only microporation led to a uniform cytosolic distribution. Microporation also yielded a transfection efficiency of 93% and an average viability of 86%. When cells microporated with MB–NeutrAvidin conjugates were examined via flow cytometry, the signal-to-background was found to be more than 3 times higher and the sensitivity nearly five times higher than unconjugated MBs. Overall, the present study introduces an improved methodology for the high-throughput detection of RNA at the single cell level

    Sub-cellular trafficking and functionality of 2\u27-O-methyl and 2\u27-O-methyl-phosphorothioate molecular beacons

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    Molecular beacons (MBs) have shown great potential for the imaging of RNAs within single living cells; however, the ability to perform accurate measurements of RNA expression can be hampered by false-positives resulting from nonspecific interactions and/or nuclease degradation. These false-positives could potentially be avoided by introducing chemically modified oligonucleotides into the MB design. In this study, fluorescence microscopy experiments were performed to elucidate the subcellular trafficking, false-positive signal generation, and functionality of 2\u27-O-methyl (2Me) and 2\u27-O-methyl-phosphorothioate (2MePS) MBs. The 2Me MBs exhibited rapid nuclear sequestration and a gradual increase in fluorescence over time, with nearly 50% of the MBs being opened nonspecifically within 24 h. In contrast, the 2MePS MBs elicited an instantaneous increase in false-positives, corresponding to ~5–10% of the MBs being open, but little increase was observed over the next 24 h. Moreover, trafficking to the nucleus was slower. After 24 h, both MBs were localized in the nucleus and lysosomal compartments, but only the 2MePS MBs were still functional. When the MBs were retained in the cytoplasm, via conjugation to NeutrAvidin, a significant reduction in false-positives and improvement in functionality was observed. Overall, these results have significant implications for the design and applications of MBs for intracellular RNA measurement

    Issues in Exploring Variation in Childhood Socioeconomic Gradients By Age: A Response to Case, Paxson, and Vogl.

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/116220/1/ssm07.pd
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