128 research outputs found

    HIV-1 Promotes Renal Tubular Epithelial Cell Protein Synthesis: Role of mTOR Pathway

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    Tubular cell HIV-infection has been reported to manifest in the form of cellular hypertrophy and apoptosis. In the present study, we evaluated the role of mammalian target of rapamycin (mTOR) pathway in the HIV induction of tubular cell protein synthesis. Mouse proximal tubular epithelial cells (MPTECs) were transduced with either gag/pol-deleted NL4-3 (HIV/MPTEC) or empty vector (Vector/MPTEC). HIV/MPTEC showed enhanced DNA synthesis when compared with Vector/MPTECs by BRDU labeling studies. HIV/MPTECs also showed enhanced production of ÎČ-laminin and fibronection in addition to increased protein content per cell. In in vivo studies, renal cortical sections from HIV transgenic mice and HIVAN patients showed enhanced tubular cell phosphorylation of mTOR. Analysis of mTOR revealed increased expression of phospho (p)-mTOR in HIV/MPTECs when compared to vector/MPTECs. Further downstream analysis of mTOR pathway revealed enhanced phosphorylation of p70S6 kinase and associated diminished phosphorylation of eEF2 (eukaryotic translation elongation factor 2) in HIV/MPTECs; moreover, HIV/MPTECs displayed enhanced phosphorylation of eIF4B (eukaryotic translation initiation factor 4B) and 4EBP-1 (eukaryotic 4E binding protein). To confirm our hypothesis, we evaluated the effect of rapamycin on HIV-induced tubular cell downstream signaling. Rapamycin not only attenuated phosphorylation of p70S6 kinase and associated down stream signaling in HIV/MPTECs but also inhibited HIV-1 induced tubular cell protein synthesis. These findings suggest that mTOR pathway is activated in HIV-induced enhanced tubular cell protein synthesis and contributes to tubular cell hypertrophy

    Generalized Poisson Summation Formulas for Continuous Functions of Polynomial Growth

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    The Poisson summation formula (PSF) describes the equivalence between the sampling of an analog signal and the periodization of its frequency spectrum. In engineering textbooks, the PSF is usually stated formally without explicit conditions on the signal for the formula to hold. By contrast, in the mathematics literature, the PSF is commonly stated and proven in the pointwise sense for various types of L1 L _{ 1 } signals. This L1 L _{ 1 } assumption is, however, too restrictive for many signal-processing tasks that demand the sampling of possibly growing signals. In this paper, we present two generalized versions of the PSF for d-dimensional signals of polynomial growth. In the first generalization, we show that the PSF holds in the space of tempered distributions for every continuous and polynomially growing signal. In the second generalization, the PSF holds in a particular negative-order Sobolev space if we further require that d∕2 + Δ derivatives of the signal are bounded by some polynomial in the L2 L _{ 2 } sense

    Constitutive modelling of skin ageing

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    The objective of this chapter is to review the main biomechanical and structural aspects associated with both intrinsic and extrinsic skin ageing, and to present potential research avenues to account for these effects in mathematical and computational models of the skin. This will be illustrated through recent work of the authors which provides a basis to those interested in developing mechanistic constitutive models capturing the mechanobiology of skin across the life course
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