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Spectral and fluorescence imaging of immune system and tissue response to an immunogenic agent

机译:免疫系统的光谱和荧光成像以及组织对免疫原性试剂的反应

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Imaging of immune system and tissue response to immunogenic agents can be important to the development of new biomaterials. Additionally, quantitative functional imaging can be useful for testing and evaluation of methods to alter or control the immune system response to implanted materials. In this preliminary study, we employ spectral imaging and fluorescence imaging to measure immune system and tissue response to implanted immunogenic agents. Poly (D,L lactide-co-glycolide) (PLGA) with a 50:50 composition was used to create immunogenic microparticles (MPs). Lipopolysaccharide (LPS) encapsulated in the MPs was used to provoke a tissue immune response in mice and encapsulated fluorescein isothiocyanate (FITC) was used to fluorescently label the MPs for imaging. Control MPs did not contain LPS. The MPs were delivered at 50 particles/μL in a total volume of 20μL by subcutaneous injection in the skin of a nude mouse in a dorsal skin-fold window chamber preparation. Cultured immune cells from a mouse leukemic monocyte macrophage cell line were exogenously labeled with the fluorescent dye DiD in solution at a concentration of 8000cells/μL. Immediately after window chamber surgery and implantation of the MPs, 100μL of the fluorescent macrophage solution was administered via the tail vein. Fluorescence imaging was used to track MPs and macrophages while spectral imaging was used for imaging and measurement of hemoglobin saturation in the tissue microvasculature. Imaging was performed periodically over about three days. The spectral and fluorescence imaging combination enabled detailed observations of the macrophage response and functional effects on the tissue.
机译:免疫系统成像和组织对免疫原性试剂的反应对于开发新的生物材料可能很重要。另外,定量功能成像可用于测试和评估改变或控制免疫系统对植入材料的反应的方法。在这项初步研究中,我们采用光谱成像和荧光成像来测量免疫系统和组织对植入的免疫原性试剂的反应。组成为50:50的聚(D,L丙交酯-乙交酯共聚物)(PLGA)用于产生免疫原性微粒(MPs)。封装在MP中的脂多糖(LPS)用于引起小鼠的组织免疫反应,封装的异硫氰酸荧光素(FITC)用于对MP进行荧光标记以进行成像。控制MP不包含LPS。通过皮下注射在背部皮肤折叠窗口小室制剂中的裸鼠皮肤中,MP以50颗粒/μL的总体积20μL递送。来自小鼠白血病单核细胞巨噬细胞系的培养免疫细胞在溶液中以8000cells /μL的浓度用荧光染料DiD外源标记。窗室手术和MP植入后,立即通过尾静脉施用100μL荧光巨噬细胞溶液。荧光成像用于跟踪MP和巨噬细胞,而光谱成像用于成像和测量组织微脉管系统中的血红蛋白饱和度。约三天定期进行成像。光谱和荧光成像的结合使得能够对巨噬细胞反应和对组织的功能作用进行详细观察。

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