152 research outputs found

    Swelling cholesteric liquid crystal shells to direct colloids at the interface

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    Cholesteric liquid crystals can exhibit spatial patterns in molecular alignment at interfaces that can be exploited for particle assembly. These patterns emerge from the competition between bulk and surface energies, tunable with the system geometry. In this work, we use the osmotic swelling of cholesteric double emulsions to assemble colloidal particles through a pathway-dependent process. Particles can be repositioned from a surface-mediated to an elasticity-mediated state through dynamically thinning the cholesteric shell at a rate comparable to that of colloidal adsorption. By tuning the balance between surface and bulk energies with the system geometry, colloidal assemblies on the cholesteric interface can be molded by the underlying elastic field to form linear aggregates. The transition of adsorbed particles from surface regions with homeotropic anchoring to defect regions is accompanied by a reduction in particle mobility. The arrested assemblies subsequently map out and stabilize topological defects. These results demonstrate the kinetic arrest of interfacial particles within definable patterns by regulating the energetic frustration within cholesterics. This work highlights the importance of kinetic pathways for particle assembly in liquid crystals, of relevance to optical and energy applications.Comment: 21 pages, 9 figures total, including 4 supplemental figure

    Prior mucosal exposure to heterologous cells alters the pathogenesis of cell-associated mucosal feline immunodeficiency virus challenge

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    <p>Abstract</p> <p>Background</p> <p>Several lines of research suggest that exposure to cellular material can alter the susceptibility to infection by HIV-1. Because sexual contact often includes exposure to cellular material, we hypothesized that repeated mucosal exposure to heterologous cells would induce an immune response that would alter the susceptibility to mucosal infection. Using the feline immunodeficiency virus (FIV) model of HIV-1 mucosal transmission, the cervicovaginal mucosa was exposed once weekly for 12 weeks to 5,000 heterologous cells or media (control) and then cats were vaginally challenged with cell-associated or cell-free FIV.</p> <p>Results</p> <p>Exposure to heterologous cells decreased the percentage of lymphocytes in the mucosal and systemic lymph nodes (LN) expressing L-selectin as well as the percentage of CD4+ CD25+ T cells. These shifts were associated with enhanced ex-vivo proliferative responses to heterologous cells. Following mucosal challenge with cell-associated, but not cell-free, FIV, proviral burden was reduced by 64% in cats previously exposed to heterologous cells as compared to media exposed controls.</p> <p>Conclusions</p> <p>The pathogenesis and/or the threshold for mucosal infection by infected cells (but not cell-free virus) can be modulated by mucosal exposure to uninfected heterologous cells.</p
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