Or Reuven, Ivan Mikula, Hadas Ashkenazi-Preiser, Nira Twaik, Kerem Ben-Meir, Yaron Meirow, Leonor Daniel, Guy Kariv, Mahdi Kurd, Michal Baniyash
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引用次数: 3
Abstract
Myeloid-derived suppressor cells (MDSCs) are heterogenous populations of immature myeloid cells that can be divided into two main subpopulations, polymorphonuclear (PMN) MDSCs and monocytic (M) MDSCs. These cells accumulate during chronic inflammation, characterizing an array of pathologies such as cancer, inflammatory bowel disease, and infectious and autoimmune diseases, and induce immunosuppression. The suppressive effects of MDSCs on the immune system are studied mainly when focusing on their features, functions, and impact on target cells such as T cells, natural killer cells, and B cells, among others. Herein, we describe methods for the analysis of MDSC immunosuppressive features and functions, measuring different mediators that contribute to their activities and how they impact on T cell function. The protocols described are a continuation to those in a companion Current Protocols article by Reuven et al. (2022), which uses a generated single-cell suspension and isolated cells to test their activity. © 2022 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Evaluating MDSC suppressive features Alternate Protocol 1: Dichlorofluorescein diacetate-based reactive oxygen species detection Support Protocol 1: Detection of nitric oxide secretion Support Protocol 2: Measurement of arginase activity Basic Protocol 2: Evaluating MDSC suppressive function Alternate Protocol 2: In vitro effects of MDSCs on expression of T cell receptor complex during activation Support Protocol 3: Effect of MDSCs on interferon γ production Basic Protocol 3: Effect of MDSCs on T cell proliferation Basic Protocol 4: Effect of MDSCs on T cell cytotoxic activity Alternate Protocol 3: In vivo cytotoxicity assay Basic Protocol 5: Analysis of MDSC differentiation.
评价髓源性抑制细胞介导的免疫抑制的功能测定。
髓源性抑制细胞(myeloid -derived suppressor cells, MDSCs)是一种异质性的未成熟髓系细胞,可分为两个主要亚群:多形核MDSCs (PMN)和单核MDSCs (M)。这些细胞在慢性炎症中积累,表现出一系列病理,如癌症、炎症性肠病、感染性和自身免疫性疾病,并诱导免疫抑制。研究MDSCs对免疫系统的抑制作用主要集中在其特征、功能以及对靶细胞如T细胞、自然杀伤细胞、B细胞等的影响。在这里,我们描述了分析MDSC免疫抑制特征和功能的方法,测量了促进其活性的不同介质以及它们如何影响T细胞功能。所描述的方案是Reuven等人(2022)在当前方案的配套文章中所述方案的延续,该文章使用生成的单细胞悬浮液和分离的细胞来测试其活性。©2022作者。目前由Wiley期刊有限责任公司发布的方案。基本方案1:评估MDSC抑制特征替代方案1:基于二氯荧光素二乙酸酯的活性氧检测支持方案1:检测一氧化氮分泌支持方案2:精氨酸酶活性测量基本方案2:评估MDSC抑制功能替代方案2:MDSCs对激活期间T细胞受体复合物表达的体外影响支持方案3:MDSCs对干扰素γ产生的影响基本方案3:MDSCs对T细胞增殖的影响基本方案4:MDSCs对T细胞细胞毒性活性的影响备选方案3:体内细胞毒性测定基本方案5:MDSC分化分析。
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