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Spectral and fluorescence imaging of immune system and tissueresponse to an immunogenic agent

机译:免疫系统的光谱和荧光成像和免疫原剂的蛋白酶

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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 204 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:对免疫系统的成像和对免疫原剂的组织反应对于新生物材料的发育可能是重要的。另外,定量功能成像可用于测试和评估方法以改变或控制免疫系统对植入材料的反应。在该初步研究中,我们采用光谱成像和荧光成像来测量免疫系统和组织反应对植入的免疫原剂。使用50:50组合物的聚(D,L丙交酯 - 共乙酰胺)(PLGA)用于产生免疫原性微粒(MPS)。在MPS中包封的脂多糖(LPS)用于引发小鼠的组织免疫应答,并使用包封荧光素异硫氰酸酯(FITC)用于荧光标记MPS进行成像。控制MPS不包含LPS。通过皮下注射在裸鼠的皮肤折叠窗户腔室制备中,通过皮下注射在50颗粒/μl以50颗粒/μl递送。将来自小鼠白细胞血细胞巨噬细胞系的培养免疫细胞随着荧光染料在溶液中以8000cells /μl的浓度进行外源标记。在窗户室外手术和植入MPS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MPS和巨噬细胞,而光谱成像用于组织微血管结构中的血红蛋白饱和的成像和测量。成像定期在大约三天内进行。光谱和荧光成像组合能够详细观察巨噬细胞响应和组织的功能效应。

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