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测定细胞因子和表面受体刺激后自然杀伤细胞的激活状态。

Determining Activation Status of Natural Killer Cells Following Stimulation via Cytokines and Surface Receptors.

机构信息

The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.

Department of Medical Biology, The University of Melbourne, Melbourne, VIC, Australia.

出版信息

Methods Mol Biol. 2022;2463:181-194. doi: 10.1007/978-1-0716-2160-8_13.

Abstract

Stimulation of Natural Killer (NK) cells with cytokines, target cell interaction, or antibody mediated activation of receptors on the NK cell surface enables the dissection of specific signaling intermediates in different activation pathways. NK cell activation status is commonly measured by production of interferon gamma (IFNγ) and expression of the degranulation marker LAMP-1 (CD107a). Cytotoxic potency can also be assessed by the production of perforin, granzymes, and tumor necrosis factor alpha (TNFα). NK cell receptor mediated activation by antibodies requires crosslinking of the receptor-specific antibodies; thus, in vitro activation assays are performed by binding antibodies to cell culture plates. All parameters can be measured by flow cytometry.

摘要

使用细胞因子刺激自然杀伤 (NK) 细胞、靶细胞相互作用或抗体介导 NK 细胞表面受体的激活,能够分离不同激活途径中的特定信号转导介质。NK 细胞激活状态通常通过产生干扰素 γ (IFNγ) 和脱颗粒标记物 LAMP-1 (CD107a) 的表达来衡量。细胞毒性效力也可以通过穿孔素、颗粒酶和肿瘤坏死因子 α (TNFα) 的产生来评估。抗体介导的 NK 细胞受体激活需要受体特异性抗体的交联;因此,体外激活实验通过将抗体结合到细胞培养板上来进行。所有参数都可以通过流式细胞术进行测量。

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