1,907 research outputs found

    Cellular kinetics of perivascular MSC precursors

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    Mesenchymal stem/stromal cells (MSCs) and MSC-like multipotent stem/progenitor cells have been widely investigated for regenerative medicine and deemed promising in clinical applications. In order to further improve MSC-based stem cell therapeutics, it is important to understand the cellular kinetics and functional roles of MSCs in the dynamic regenerative processes. However, due to the heterogeneous nature of typical MSC cultures, their native identity and anatomical localization in the body have remained unclear, making it difficult to decipher the existence of distinct cell subsets within the MSC entity. Recent studies have shown that several blood-vessel-derived precursor cell populations, purified by flow cytometry from multiple human organs, give rise to bona fide MSCs, suggesting that the vasculature serves as a systemic reservoir of MSC-like stem/progenitor cells. Using individually purified MSC-like precursor cell subsets, we and other researchers have been able to investigate the differential phenotypes and regenerative capacities of these contributing cellular constituents in the MSC pool. In this review, we will discuss the identification and characterization of perivascular MSC precursors, including pericytes and adventitial cells, and focus on their cellular kinetics: cell adhesion, migration, engraftment, homing, and intercellular cross-talk during tissue repair and regeneration. © 2013 William C. W. Chen et al

    Cellular kinetics of perivascular MSC precursors

    Get PDF
    Mesenchymal stem/stromal cells (MSCs) and MSC-like multipotent stem/progenitor cells have been widely investigated for regenerative medicine and deemed promising in clinical applications. In order to further improve MSC-based stem cell therapeutics, it is important to understand the cellular kinetics and functional roles of MSCs in the dynamic regenerative processes. However, due to the heterogeneous nature of typical MSC cultures, their native identity and anatomical localization in the body have remained unclear, making it difficult to decipher the existence of distinct cell subsets within the MSC entity. Recent studies have shown that several blood-vessel-derived precursor cell populations, purified by flow cytometry from multiple human organs, give rise to bona fide MSCs, suggesting that the vasculature serves as a systemic reservoir of MSC-like stem/progenitor cells. Using individually purified MSC-like precursor cell subsets, we and other researchers have been able to investigate the differential phenotypes and regenerative capacities of these contributing cellular constituents in the MSC pool. In this review, we will discuss the identification and characterization of perivascular MSC precursors, including pericytes and adventitial cells, and focus on their cellular kinetics: cell adhesion, migration, engraftment, homing, and intercellular cross-talk during tissue repair and regeneration. © 2013 William C. W. Chen et al

    Análisis de preferencias turísticas: un enfoque innovador

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    Most of the decisions concerning tourism are made in a context of uncertainty, and on several occasions the consequences of the choice are not known with certainty, or even there is missing information on this matter. For these reasons, the fuzzy set theory is an appropriate tool for their treatments.In this paper we show, through a case study, an alternative model for the analysis of tourist preferences of a segment of individuals based on the concept of fuzzy consideration set.La mayor parte de las decisiones referidas a turismo se toman en un contexto de incertidumbre, y en muchas oportunidades no se conocen con certeza las consecuencias de la elección, ni se posee toda la información. Por estas razones la teoría de conjuntos borrosos resulta una herramienta apropiada para su tratamiento.En este trabajo se presenta, a través del estudio de un caso, un modelo alternativo para el análisis de las preferencias turísticas, de un segmento de individuos, basado en el concepto de conjunto de consideración borroso

    Mechanisms involved in the promoting activity of fibroblasts in HTLV-1-mediated lymphomagenesis: Insights into the plasticity of lymphomatous cells

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    Among the mechanisms leading to progression to Adult T-cell Leukaemia/Lymphoma in Human T-cell Leukaemia Virus type 1 (HTLV-1)-infected subjects, the contribution of stromal components remains poorly understood. To dissect the role of fibroblasts in HTLV-1-mediated lymphomagenesis, transcriptome studies, cytofluorimetric and qRT-PCR analyses of surface and intracellular markers linked to plasticity and stemness in coculture, and in vivo experiments were performed. A transcriptomic comparison between a more lymphomagenic (C91/III) and the parental (C91/PL) cell line evidenced hyperactivation of the PI3K/Akt pathway, confirmed by phospho-ELISA and 2-DE and WB analyses. C91/III cells also showed higher expression of mesenchymal and stemness genes. Short-term coculture with human foreskin fibroblasts (HFF) induced these features in C91/PL cells, and significantly increased not only the cancer stem cells (CSCs)-supporting CD10+GPR77+ HFF subpopulation, but also the percentage of ALDH1bright C91/PL cells. A non-cytotoxic acetylsalicylic acid treatment decreased HFF-induced ALDH1bright C91/PL cells, downregulated mesenchymal and stemness genes in cocultured cells, and delayed lymphoma growth in immunosuppressed mice, thus hindering the supportive activity of HFF on CSCs. These data suggest that crosstalk with HFF significantly intensifies the aggressiveness and plasticity of C91/PL cells, leading to the enrichment in lymphoma-initiating cells. Additional research is needed to better characterize these preliminary findings

    Muons and emissivities of neutrinos in neutron star cores

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    In this work we consider the role of muons in various URCA processes relevant for neutrino emissions in the core region of neutron stars. The calculations are done for β\beta--stable nuclear matter with and without muons. We find muons to appear at densities ρ=0.15\rho = 0.15 fm3^{-3}, slightly around the saturation density for nuclear matter ρ0=0.16\rho_0 =0.16 fm3^{-3}. The direct URCA processes for nucleons are forbidden for densities below ρ=0.5\rho = 0.5 fm3^{-3}, however the modified URCA processes with muons (n+Np+N+μ+νμ,p+N+μn+N+νμ(n+N\rightarrow p+N +\mu +\overline{\nu}_{\mu}, p+N+\mu \rightarrow n+N+\nu_{\mu}), where NN is a nucleon, result in neutrino emissivities comparable to those from (n+Np+N+e+νe,p+N+en+N+νe(n+N\rightarrow p+N +e +\overline{\nu}_e, p+N+e \rightarrow n+N+\nu_e). This opens up for further possibilities to explain the rapid cooling of neutrons stars. Superconducting protons reduce however these emissivities at densities below 0.40.4 fm3^{-3}.Comment: 14 pages, Revtex style, 3 uuencoded figs include
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