72 research outputs found

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    Epithelial coxsackievirus adenovirus receptor promotes house dust mite-induced lung inflammation

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    Airway inflammation and remodelling are important pathophysiologic features in asthma and other respiratory conditions. An intact epithelial cell layer is crucial to maintain lung homoeostasis, and this depends on intercellular adhesion, whilst damaged respiratory epithelium is the primary instigator of airway inflammation. The Coxsackievirus Adenovirus Receptor (CAR) is highly expressed in the epithelium where it modulates cell-cell adhesion stability and facilitates immune cell transepithelial migration. However, the contribution of CAR to lung inflammation remains unclear. Here we investigate the mechanistic contribution of CAR in mediating responses to the common aeroallergen, House Dust Mite (HDM). We demonstrate that administration of HDM in mice lacking CAR in the respiratory epithelium leads to loss of peri-bronchial inflammatory cell infiltration, fewer goblet-cells and decreased pro-inflammatory cytokine release. In vitro analysis in human lung epithelial cells confirms that loss of CAR leads to reduced HDM-dependent inflammatory cytokine release and neutrophil migration. Epithelial CAR depletion also promoted smooth muscle cell proliferation mediated by GSK3ÎČ and TGF-ÎČ, basal matrix production and airway hyperresponsiveness. Our data demonstrate that CAR coordinates lung inflammation through a dual function in leucocyte recruitment and tissue remodelling and may represent an important target for future therapeutic development in inflammatory lung diseases

    Justicia conciliatoria durante el liberalismo hispano en el PerĂș: el caso de Huamanga

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    The 1812 Constitution established the division of powers, except at local level. Mayors held powers in the internal government of towns and villages and were lay judges in settlements, an obligatory procedure for litigants and for resolving any dispute before the legal courts —district or provincial judges. Based on the case study of Huamanga, the pla - yers and the type of causes settled during the two stages in which the vice-royalty of Peru practised Spanish liberal politics —1812-1814 and 1820-1824— are analysed. The muni - cipal judicial culture was dominated by a series of changes and demands, which provide new perspectives towards an understanding of the convulsed times of the wars of indepen - dence of the Andes that sometimes extended to the early republic.La ConstituciĂłn de 1812 estableciĂł la divisiĂłn de poderes, excepto en el ĂĄmbito local. Los alcaldes tenĂ­an competencias en el gobierno interior de los pueblos y, al mismo tiempo, eran los jueces legos en las conciliaciones, un trĂĄmite preceptivo para los litigantes y para dirimir cualquier conflicto ante la justicia letrada —jueces de partido o audiencias. A partir del estudio de caso de Huamanga, se analizan los actores y la tipologĂ­a de las causas dirimidas durante las dos etapas en que el virreinato del PerĂș ensayĂł la polĂ­tica liberal hispana —1812-1814 y 1820-1824. La cultura jurĂ­dica municipal estuvo dominada por una serie de cambios y reivindicaciones, que aportan nuevas perspectivas para comprender los convulsos tiempos de las guerras por la independencia en los Andes y que en ocasiones trascendieron a la temprana repĂșblica

    Plk1 regulates mitotic Aurora A function through ÎČTrCP-dependent degradation of hBora

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    Polo-like kinase 1 (Plk1) and Aurora A play key roles in centrosome maturation, spindle assembly, and chromosome segregation during cell division. Here we show that the functions of these kinases during early mitosis are coordinated through Bora, a partner of Aurora A first identified in Drosophila. Depletion of human Bora (hBora) results in spindle defects, accompanied by increased spindle recruitment of Aurora A and its partner TPX2. Conversely, hBora overexpression induces mislocalization of Aurora A and monopolar spindle formation, reminiscent of the phenotype seen in Plk1-depleted cells. Indeed, Plk1 regulates hBora. Following Cdk1-dependent recruitment, Plk1 triggers hBora destruction by phosphorylating a recognition site for \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}SCF ÎČ - TrCP{\text{SCF}}^{{\text{ $ \beta $ - TrCP}}} \end{document}. Plk1 depletion or inhibition results in a massive accumulation of hBora, concomitant with displacement of Aurora A from spindle poles and impaired centrosome maturation, but remarkably, co-depletion of hBora partially restores Aurora A localization and bipolar spindle formation. This suggests that Plk1 controls Aurora A localization and function by regulating cellular levels of hBora

    Diffusion model comparison identifies distinct tumor sub-regions and tracks treatment response.

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    PURPOSE:MRI biomarkers of tumor response to treatment are typically obtained from parameters derived from a model applied to pre-treatment and post-treatment data. However, as tumors are spatially and temporally heterogeneous, different models may be necessary in different tumor regions, and model suitability may change over time. This work evaluates how the suitability of two diffusion-weighted (DW) MRI models varies spatially within tumors at the voxel level and in response to radiotherapy, potentially allowing inference of qualitatively different tumor microenvironments. METHODS:DW-MRI data were acquired in CT26 subcutaneous allografts before and after radiotherapy. Restricted and time-independent diffusion models were compared, with regions well-described by the former hypothesized to reflect cellular tissue, and those well-described by the latter expected to reflect necrosis or oedema. Technical and biological validation of the percentage of tissue described by the restricted diffusion microstructural model (termed %MM) was performed through simulations and histological comparison. RESULTS:Spatial and radiotherapy-related variation in model suitability was observed. %MM decreased from a mean of 64% at baseline to 44% 6 days post-radiotherapy in the treated group. %MM correlated negatively with the percentage of necrosis from histology, but overestimated it due to noise. Within MM regions, microstructural parameters were sensitive to radiotherapy-induced changes. CONCLUSIONS:There is spatial and radiotherapy-related variation in different models' suitability for describing diffusion in tumor tissue, suggesting the presence of different and changing tumor sub-regions. The biological and technical validation of the proposed %MM cancer imaging biomarker suggests it correlates with, but overestimates, the percentage of necrosis
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