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首页> 外文期刊>Frontiers in Immunology >Defining Genome-Wide Expression and Phenotypic Contextual Cues in Macrophages Generated by Granulocyte/Macrophage Colony-Stimulating Factor, Macrophage Colony-Stimulating Factor, and Heat-Killed Mycobacteria
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Defining Genome-Wide Expression and Phenotypic Contextual Cues in Macrophages Generated by Granulocyte/Macrophage Colony-Stimulating Factor, Macrophage Colony-Stimulating Factor, and Heat-Killed Mycobacteria

机译:定义由粒细胞/巨噬细胞集落刺激因子,巨噬细胞集落刺激因子和热杀分枝杆菌产生的巨噬细胞中的基因组表达和表型上下文提示

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Heat-killed (HK) Mycobacterium obuense (NCTC13365) is currently being evaluated in the clinic as an immunotherapeutic agent for cancer treatment. Yet, the molecular underpinnings underlying immunomodulatory properties of HK M. obuense are still largely undefined. To fill this void, we sought to perform immunophenotyping, chemokine/cytokine release analysis and genome-wide characterization of monocyte-derived macrophages (MDM) in which monocytes were originally isolated from healthy donors and differentiated by HK M. obuense (Mob-MDM) relative to macrophage colony-stimulating factor (M-MDM) and granulocyte/macrophage colony-stimulating factor (GM-MDM). Immunophenotyping and cytokine release analysis revealed downregulated surface expression of CD36, decreased spontaneous release of CCL2 and increased spontaneous secretion of CCL5, CXCL8/IL-8, IL-6, and TNF-α in Mob-MDM relative to M-MDM and GM-MDM. Analysis of cytostatic activity showed that Mob-MDM exhibited similar growth inhibitory effects on immortalized and malignant epithelial cells compared with GM-MDM but at an elevated rate relative to M-MDM. To understand global cues in Mob-MDM, we performed comparative RNA-sequencing (RNA-Seq) analysis of Mob-MDM relative to GM-MDM and M-MDM ( n ?=?4 donors). Clustering analysis underscored expression profiles ( n ?=?256) that were significantly modulated in Mob-MDM versus both M-MDM and GM-MDM including, among others, chemokines/cytokines and their receptors, enzymes and transcriptions factors. Topological functional analysis of these profiles identified pathways and gene sets linked to Mob-MDM phenotype including nitric oxide production, acute phase response signaling and microbe recognition pathways as well as signaling cues mediated by the proinflammatory cytokine, interferon-gamma, and the intracellular pattern recognition receptor, nucleotide-binding oligomerization domain-containing protein 2. Taken together, our study highlights molecular immune phenotypes and global signaling cues in Mob-MDM that may underlie immunomodulatory properties of HK M. obuense . Such properties could be of valuable use in immunotherapy approaches such as adoptive cell therapy against cancer.
机译:目前,临床上正在评估热杀死的(香港)奥布分枝杆菌(NCTC13365)作为用于癌症治疗的免疫治疗剂。然而,尚不能确定隐喻HK M. obuense的免疫调节特性的分子基础。为了填补这一空白,我们寻求进行单核细胞衍生的巨噬细胞(MDM)的免疫表型分析,趋化因子/细胞因子释放分析和全基因组表征,其中单核细胞最初是从健康供体中分离出来的,并由ob Muense(Mob-MDM)分化而来。相对于巨噬细胞集落刺激因子(M-MDM)和粒细胞/巨噬细胞集落刺激因子(GM-MDM)。免疫分型和细胞因子释放分析表明,相对于M-MDM和GM-,Mob-MDM中CD36的表面表达下调,CCL2的自发释放减少以及CCL5,CXCL8 / IL-8,IL-6和TNF-α的自发分泌增加。 MDM。细胞抑制活性的分析表明,与GM-MDM相比,Mob-MDM对永生和恶性上皮细胞表现出相似的生长抑制作用,但相对于M-MDM而言,其抑制率较高。为了了解Mob-MDM的整体线索,我们对Mob-MDM相对于GM-MDM和M-MDM(n == 4个供体)进行了比较RNA测序(RNA-Seq)分析。聚类分析强调了在Mob-MDM中与M-MDM和GM-MDM相比,在Mob-MDM中得到显着调节的表达谱(n = 256),其中包括趋化因子/细胞因子及其受体,酶和转录因子。这些配置文件的拓扑功能分析确定了与Mob-MDM表型相关的途径和基因集,包括一氧化氮的产生,急性期反应信号传导和微生物识别途径以及促炎性细胞因子,干扰素-γ和细胞内模式识别介导的信号暗示受体,核苷酸结合的低聚域蛋白2。综上所述,我们的研究突出了Mob-MDM中的分子免疫表型和整体信号提示,这可能是对厚实梭状芽胞杆菌免疫调节特性的基础。这样的性质在免疫疗法中可能是有价值的用途,例如针对癌症的过继细胞疗法。

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