{"title":"Isolation and Functional Use of Human NKT Cells","authors":"Mark A. Exley, S. Brian Wilson, Steven P. Balk","doi":"10.1002/cpim.33","DOIUrl":null,"url":null,"abstract":"<p>This unit details methods for the isolation, <i>in vitro</i> expansion, and functional characterization of human iNKT cells. The term ‘iNKT’ derives from the fact that a large fraction of murine and some human NK marker+ T cells (‘NKT’) recognize the MHC class I–like CD1d protein and use an identical ‘invariant’ TCRα chain, which is generated in humans by precise Vα24 and Jα18 rearrangements with either no N-region diversity or subsequent trimming to identical or nearly identical amino acid sequence (hence, ‘iNKT’ cells). iNKT are mostly CD4+ or CD4–CD8– (‘double negative’), although a few CD8+ iNKT can be found in some humans. Basic Protocol 1 and Alternate Protocol 1 use multi-color FACS analysis to identify and quantitate rare iNKT cells from human samples. Basic Protocol 2 describes iNKT cell purification. Alternate Protocol 2 describes a method for high-speed FACS sorting of iNKT cells. Basic Protocol 3 explains functional analysis of iNKT. Alternate Protocol 3 employs a cell sorting approach to isolate iNKT cell clones. A support protocol for secondary stimulation and rapid expansion of iNKT cells is also included. © 2017 by John Wiley & Sons, Inc.</p>","PeriodicalId":10733,"journal":{"name":"Current Protocols in Immunology","volume":"119 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpim.33","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Immunology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpim.33","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 8
Abstract
This unit details methods for the isolation, in vitro expansion, and functional characterization of human iNKT cells. The term ‘iNKT’ derives from the fact that a large fraction of murine and some human NK marker+ T cells (‘NKT’) recognize the MHC class I–like CD1d protein and use an identical ‘invariant’ TCRα chain, which is generated in humans by precise Vα24 and Jα18 rearrangements with either no N-region diversity or subsequent trimming to identical or nearly identical amino acid sequence (hence, ‘iNKT’ cells). iNKT are mostly CD4+ or CD4–CD8– (‘double negative’), although a few CD8+ iNKT can be found in some humans. Basic Protocol 1 and Alternate Protocol 1 use multi-color FACS analysis to identify and quantitate rare iNKT cells from human samples. Basic Protocol 2 describes iNKT cell purification. Alternate Protocol 2 describes a method for high-speed FACS sorting of iNKT cells. Basic Protocol 3 explains functional analysis of iNKT. Alternate Protocol 3 employs a cell sorting approach to isolate iNKT cell clones. A support protocol for secondary stimulation and rapid expansion of iNKT cells is also included. © 2017 by John Wiley & Sons, Inc.
人NKT细胞的分离与功能应用
本单元详细介绍了人类iNKT细胞的分离、体外扩增和功能表征方法。术语“iNKT”源于这样一个事实,即大部分小鼠和一些人类NK标记+ T细胞(“NKT”)识别MHC类I-like CD1d蛋白并使用相同的“不变”TCRα链,该链在人类中通过精确的Vα24和Jα18重排产生,要么没有n区多样性,要么随后修整为相同或几乎相同的氨基酸序列(因此,“iNKT”细胞)。iNKT主要是CD4+或CD4 - CD8 -(“双阴性”),尽管在一些人身上可以发现少量CD8+ iNKT。基本方案1和备选方案1使用多色FACS分析从人类样本中鉴定和定量稀有iNKT细胞。基本方案2描述iNKT细胞纯化。备选方案2描述了一种iNKT细胞的高速FACS分选方法。基本协议3解释了iNKT的功能分析。备选方案3采用细胞分选方法分离iNKT细胞克隆。还包括iNKT细胞二次刺激和快速扩增的支持方案。©2017 by John Wiley &儿子,Inc。
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