682 research outputs found

    ASSESSING EAR PINNA REPAIR IN THE MRL/MpJ MOUSE STRAIN

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    The outcome of tissue repair varies across species. Vertebrates such as salamanders have the ability to not only heal scar-free but also completely regenerate lost appendages. In contrast, most mammals heal their wounds with fibrotic scarring. Understanding the key drivers of these divergent injury responses remains a major unanswered question in animal biology. Previous work with the Murphy’s Roth Large (MRL/MpJ) inbred mouse strain suggested they have the ability to rapidly close small (2mm) ear holes. While this ability was originally published as an example of regeneration, subsequent work by other groups suggested that it might represent something more akin to hyper-fibrosis. Thus, the ability of MRL/MpJ mice to heal ear hole punches by regeneration or via fibrotic repair (scarring) remains unresolved. The purpose of this study was to analyze ear hole closure in the MRL/MpJ strain across a range of hole sizes and to characterize the healing process. Moreover, I tested multiple hypotheses that could explain the rapid closure of small ear holes, including MRL/MpJ mice exhibit enhanced cell proliferation, increased ECM gene expression, synthesis, and deposition, and that they exhibit hyperinflammation compared to control outbred strains. We found marginal, albeit weak, support for all three hypotheses supporting faster closure of ear punch injuries but did not find evidence of tissue regeneration

    Near-Infrared Fluorescent Carbon Nanotubes; A New Paradigm in Disease Detection and Biological Imaging

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    The bandgap near-infrared photoluminescence from the semiconducting single-walled carbon nanotubes is photostable, tunable, and sensitive to the local environment. Over the last 15 years, significant progress has been made in applying carbon nanotube photoluminescence toward a range of in vitro and in vivo biomedical applications. My research at URI NanoBio Engineering Lab encompasses the design and implementation of implantable and wearable biosensors in addition to developing in vitro molecular probes, based on single-walled carbon nanotubes. We engineer the molecular corona of the SWCNTs to significantly enhance their selectivity to multiple disease biomarkers, so their spectral variations can be utilized for biomarker detection and quantification, down to nanomolar concentrations. We then embed these nanomaterials into biocompatible scaffolds to provide implantable and wearable sensing platforms. We also utilize a variety of imaging, spectroscopy, and other analytical techniques to investigate the fundamental interactions between our engineered nanomaterials and biological systems. Using a specialized near-infrared fluorescence hyperspectral imaging system, we are able to collect the emission spectra from single carbon nanotubes within live cells. By fully characterizing these types of nanobio interactions, we aim to construct highly robust bio-analytical probes while simultaneously mitigating toxicological concerns

    Nondegeneracy of the spectrum of the twisted cocycle for interval exchange transformations

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    We prove the positivity of the top Lyapunov exponent of the twisted (spectral) cocycle, associated with IETs, with respect to a family of natural invariant measures. The proof relies on relating the top exponent to limits of exponents along families of affine invariant submanifolds of genus tending to infinity. Applications include an observation about a conjecture of Kontsevich and Zorich, a discrepancy estimate, and a formula for the lower local dimension of spectral measures

    Impact of Human Immunodeficiency Virus in the Pathogenesis and Outcome of Patients with Glioblastoma Multiforme.

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    BackgroundImprovement in antiviral therapies have been accompanied by an increased frequency of non-Acquired Immune Deficiency Syndrome (AIDS) defining malignancies, such as glioblastoma multiforme. Here, we investigated all reported cases of human immunodeficiency virus (HIV)-positive patients with glioblastoma and evaluated their clinical outcomes. A comprehensive review of the molecular pathogenetic mechanisms underlying glioblastoma development in the setting of HIV/AIDS is provided.MethodsWe performed a PubMed search using keywords "HIV glioma" AND "glioblastoma," and "AIDS glioma" AND "glioblastoma." Case reports and series describing HIV-positive patients with glioblastoma (histologically-proven World Health Organization grade IV astrocytoma) and reporting on HAART treatment status, clinical follow-up, and overall survival (OS), were included for the purposes of quantitative synthesis. Patients without clinical follow-up data or OS were excluded. Remaining articles were assessed for data extraction eligibility.ResultsA total of 17 patients met our inclusion criteria. Of these patients, 14 (82.4%) were male and 3 (17.6%) were female, with a mean age of 39.5±9.2 years (range 19-60 years). Average CD4 count at diagnosis of glioblastoma was 358.9±193.4 cells/mm3. Tumor progression rather than AIDS-associated complications dictated patient survival. There was a trend towards increased median survival with HAART treatment (12.0 vs 7.5 months, p=0.10).ConclusionOur data suggests that HAART is associated with improved survival in patients with HIV-associated glioblastoma, although the precise mechanisms underlying this improvement remain unclear
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