Muul Linda Mesler, Silvin Christopher, James Stephen P, Candotti Fabio
GMBB, National Human Genome Institute, Bethesda, Maryland, USA.
Curr Protoc Immunol. 2008 Aug;Chapter 7:Unit 7.10.1-7.10.24. doi: 10.1002/0471142735.im0710s82.
Measurement of proliferative responses of human lymphocytes is a fundamental technique for the assessment of their biological responses to various stimuli. Most simply, this involves measurement of the number of cells present in a culture before and after the addition of a stimulating agent. This unit contains several different prototype protocols to measure the proliferative response of lymphocytes following exposure to mitogens, antigens, allogeneic or autologous cells, or soluble factors. Each of these protocols can be used in conjunction with an accompanying support protocol which contains methods for pulsing cultures with [3H]thymidine and determining incorporation of [3H]thymidine into DNA or assessing cell proliferation by nonradioactive methods, e.g., reduction of tetrazolium salts (MTT). The protocols described here provide an estimate of DNA synthesis and cell proliferation in an entire cell population, but do not provide information on the proliferation of individual cells. A protocol for CFSE labeling allows specific subpopulations of cells to be separated viably for further analysis.
测量人类淋巴细胞的增殖反应是评估其对各种刺激的生物学反应的一项基本技术。最简单的方法是,这涉及测量添加刺激剂前后培养物中存在的细胞数量。本单元包含几种不同的原型方案,用于测量淋巴细胞在接触有丝分裂原、抗原、同种异体或自体细胞或可溶性因子后的增殖反应。这些方案中的每一个都可以与一个配套的支持方案一起使用,该支持方案包含用[3H]胸腺嘧啶核苷脉冲培养物并确定[3H]胸腺嘧啶核苷掺入DNA的方法,或通过非放射性方法(例如四唑盐还原法(MTT))评估细胞增殖的方法。这里描述的方案提供了整个细胞群体中DNA合成和细胞增殖的估计,但不提供关于单个细胞增殖的信息。CFSE标记方案允许对特定的细胞亚群进行可行的分离,以便进一步分析。