标题: 奈米钻石在胚胎癌干细胞之神经分化作用的生物相容性及标定应用
Biocompatibility and labeling application of neuronal differentiation in embryonic carcinoma stem cells using nanodiamond
作者: 徐子加
Hsu, Tzu-Chia
赵瑞益
Chao, Jui-I
分子医学与生物工程研究所
关键字: 萤光奈米钻石;胚胎癌干细胞;神经分化;神经细胞;fluorescent nanodiamond;embryonic carcinoma stem cells;neuronal differentiation;neuronal cells
公开日期: 2012
摘要: 奈米钻石是一种相当具有潜力的碳奈米材料,目前已被开发作为生物医学的应用,例如药物运送及生物标定。在本论文中,我们发现萤光奈米钻石是一种具有生物相容性及可被检测的奈米材料,可应用作为胚胎癌干细胞之神经分化作用的标定。萤光奈米钻石不会影响老鼠P19及人类NT2/D1两种胚胎癌干细胞株的细胞型态、存活率、生长能力及细胞凋亡。胚胎癌干细胞在处理0.1至50 μg/ml的萤光奈米钻石24小时后,细胞内的萤光强度会随着萤光奈米钻石之浓度增加而增高。萤光奈米钻石会进入这些细胞中,萤光奈米钻石会存在胚胎癌干细胞之细胞质中,并与SSEA-1蛋白(干细胞标志)位于相同位置。然而,萤光奈米钻石并不会显着改变胚胎癌干细胞中的SSEA-1蛋白表现。胚胎癌干细胞可利用处理视黄酸而诱导细胞进行神经分化的作用。但在分化过程中的神经细胞,萤光奈米钻石的存在并会不影响神经细胞的型态及TUJ1(神经细胞标志)的基因与蛋白表现。此外,萤光奈米钻石不会诱发神经分化过程中的细胞毒性与细胞凋亡。萤光奈米钻石也不会诱发神经细胞细胞毒性及细胞凋亡。再者,萤光奈米钻石可利用共轭焦显微镜与流式细胞仪进行这些分化的神经细胞的检测及分析。综合以上结果,我们的研究提供萤光奈米钻石是一种具有生物相容性及生物影像的标定剂,可应用于干细胞之神经分化过程的追踪。
Nanodiamond (ND) is a promising carbon nanomaterial that has been developed for biomedical applications such as drug delivery and bio-labeling. In this study, we show fluorescent nanodiamond (FND) that is a biocompatible and detectable nanomaterial, which can be used for the labeling of neuronal differentiation in embryonic carcinoma stem (ECS) cells. FND did not alter cell morphology, viability, growth ability and apoptotic levels in both the mouse P19 and human NT2/D1 ECS cells. The fluorescence intensities were increased via a concentration-dependent manner by treatment with FND (0.1-50 μg/ml for 24 h) in these ECS cells. FND particles were taken into cells. FND was co-localized with SSEA-1 protein (stem cell marker) in the cytoplasm of ECS cells. However, FND treatment did not significantly alter the SSEA-1 protein levels in ECS cells. The neuronal differentiation of ECS cells was induced by retinoic acid (RA) treatment. The existence of FND in cells did not alter the neuronal cell morphology and the gene and protein expressions of TUJ1 (neuron marker). Besides, FND did not induce cytotoxicity and apoptosis during the process of neuronal differentiation. Also, FND did not induce cytotoxicity and apoptosis in neuronal cells. Furthermore, these differentiated neuronal cells carry FND particles, which can be detected by confocal microscope and flow cytometry. Together, our findings demonstrate that FND is a biocompatible and bio-imaging agent for the labeling and tracking in the neuronal differentiation of stem cells.
URI: http://140.113.39.130/cdrfb3/record/nctu/#GT070057102
http://hdl.handle.net/11536/72314
显示于类别:Thesis