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人自然杀伤细胞的分离及淋巴因子激活的杀伤细胞活性的产生。

Isolation of human NK cells and generation of LAK activity.

作者信息

Whiteside T L

机构信息

University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

出版信息

Curr Protoc Immunol. 2001 May;Chapter 7:Unit 7.7. doi: 10.1002/0471142735.im0707s17.

Abstract

This unit describes the preparation of natural killer (NK) cells from normal human peripheral blood and their incubation in vitro in the presence of interleukin 2 (IL-2) to yield lymphokine-activated killer (LAK) cells. A protocol is presented for isolating highly purified NK cell populations from PBMC, and another method presents steps for generating LAK cells from these purified NK cells via IL-2 stimulation. An alternate protocol describes the generation of LAK cells directly from whole, unseparated PBMC preparations instead of purified NK populations. The caveat with the alternate protocol is that LAK activity generated in this manner represents the total cytotoxic potential of all LAK precursor cells--i.e., all those PBMC that are capable of responding to IL-2 by up-regulation of cytotoxicity against NK-resistant targets. In PBMC, LAK precursor cells are found among subpopulations of both NK cells and T lymphocytes.

摘要

本单元描述了从正常人外周血中制备自然杀伤(NK)细胞,并在白细胞介素2(IL-2)存在的情况下于体外培养这些细胞以产生淋巴因子激活的杀伤(LAK)细胞的方法。文中给出了从外周血单个核细胞(PBMC)中分离高度纯化的NK细胞群体的方案,以及另一种从这些纯化的NK细胞通过IL-2刺激产生LAK细胞的方法步骤。另一种方案描述了直接从未经分离的完整PBMC制剂而非纯化的NK群体中产生LAK细胞。该替代方案的注意事项是,以这种方式产生的LAK活性代表了所有LAK前体细胞的总细胞毒性潜能,即所有那些能够通过上调对NK抗性靶标的细胞毒性来响应IL-2的PBMC。在PBMC中,LAK前体细胞存在于NK细胞和T淋巴细胞的亚群中。

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