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人自然杀伤细胞亚群之间的细胞表面组织蛋白酶G活性存在差异。

Cell surface cathepsin G activity differs between human natural killer cell subsets.

作者信息

Penczek Adriane, Sienczyk Marcin, Wirtz Christian Rainer, Burster Timo

机构信息

Department of Neurosurgery, Ulm University Medical Center, Ulm, Germany.

Faculty of Chemistry, Wroclaw University of Technology, Wroclaw, Poland.

出版信息

Immunol Lett. 2016 Nov;179:80-84. doi: 10.1016/j.imlet.2016.09.010. Epub 2016 Sep 24.

Abstract

Natural killer (NK) cells are critical in diverse defense mechanisms, including elimination of viral infected cells and destruction of tumor cells. NK cells are characterized by the ability to initiate apoptosis in target cells when their cell surface major histocompatibility complex class I (MHC I) repertoire is missing. On the other hand, NK cells are not activated when MHC I or non-classical MHC molecules are found on the respective cells. It was demonstrated that cathepsin G (CatG) binds to the cell surface of NK cells; however, the distribution of this protease on the cell surface of NK cell subsets has not been identified. Here, we show that CatG cell surface level differs between NK cell subsets. CatG was determined on the protein- and activity level (activity-based probe MARS116) by using flow cytometry. Thus, MARS116 is a novel reporter of cell surface CatG activity and can be used to differentiate between distinct NK cell subsets.

摘要

自然杀伤(NK)细胞在多种防御机制中起着关键作用,包括清除病毒感染细胞和破坏肿瘤细胞。NK细胞的特征在于,当它们的细胞表面主要组织相容性复合体I类(MHC I)成分缺失时,能够启动靶细胞的凋亡。另一方面,当在相应细胞上发现MHC I或非经典MHC分子时,NK细胞不会被激活。已证明组织蛋白酶G(CatG)与NK细胞的细胞表面结合;然而,这种蛋白酶在NK细胞亚群细胞表面的分布尚未明确。在这里,我们表明CatG的细胞表面水平在NK细胞亚群之间存在差异。通过流式细胞术在蛋白质和活性水平(基于活性的探针MARS116)上测定了CatG。因此,MARS116是细胞表面CatG活性的一种新型报告分子,可用于区分不同的NK细胞亚群。

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