Durward Marina, Harms Jerome, Splitter Gary
Pathology and Laboratory Medicine, University of Wisconsin-Madison, USA.
J Vis Exp. 2010 Nov 9(45):2250. doi: 10.3791/2250.
Carboxyfluorescein diacetate succinimidyl ester (CFSE) can be used to easily and quickly label a cell population of interest for in vivo investigation. This labeling has classically been used to study proliferation and migration. In the method presented here, we have shortened the timeline after adoptive transfer to look at survival and killing of epitope specific CFSE labeled target cells. The level of specific killing of a CD8 + T cell clone can indicate the quality of the response, as their quantity may be misleading. Specific CD8+ T cells can become functionally exhausted over time with a decline in cytokine production and killing. Also, certain CD8 + T cell clones may not kill as well as others with differing TCR specificities. For effective Cell Mediated Immunity (CMI), antigens must be identified that produce not only adequate numbers of responding T cells, but also functionally robust responding T cells. Here we assess the percent cell specific killing of two peptide specific T cell clones in BALB/c mice.
羧基荧光素二乙酸琥珀酰亚胺酯(CFSE)可用于轻松快速地标记感兴趣的细胞群体,以进行体内研究。这种标记传统上用于研究细胞增殖和迁移。在此处介绍的方法中,我们缩短了过继转移后的时间线,以观察表位特异性CFSE标记的靶细胞的存活和杀伤情况。CD8 + T细胞克隆的特异性杀伤水平可表明反应的质量,因为其数量可能会产生误导。随着时间的推移,特定的CD8 + T细胞可能会在功能上耗尽,细胞因子产生和杀伤能力下降。此外,某些CD8 + T细胞克隆的杀伤能力可能不如具有不同TCR特异性的其他克隆。为了实现有效的细胞介导免疫(CMI),必须鉴定出不仅能产生足够数量的反应性T细胞,而且能产生功能强大的反应性T细胞的抗原。在此,我们评估了BALB/c小鼠中两个肽特异性T细胞克隆的细胞特异性杀伤百分比。