RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A 41-marker 37-color full spectrum flow cytometry panel for the deep immunophenotyping of human peripheral and liver natural killer cells.
A 41-marker 37-color full spectrum flow cytometry panel for the deep immunophenotyping of human peripheral and liver natural killer cells.
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NK 细胞(NK 细胞)是具有细胞毒性活性的颗粒性淋巴细胞,在固有免疫和适应性免疫应答中均发挥作用。NK 细胞由多种表型组成,其特定功能由微环境赋予。肝脏 NK 细胞是丰富的淋巴细胞群体,在生理和病理条件下对免疫应答的调节起关键作用。例如,NK 细胞的功能和表型变化发生在肝癌进展过程中,并与疾病预后相关。由于肝癌在实体癌中死亡率位居第二,因此明确健康和疾病状态下肝脏及外周 NK 细胞区室的组成和动态变化非常重要。深入分析 NK 细胞的表型、功能状态及其频率,将拓展我们对它们在维持免疫耐受、疾病进展中作用的认识,并有助于新型治疗方法的开发。
我们在此展示一个 41 标记 37 色光谱流式细胞术 panel,用于深入分析人外周和肝脏 NK 细胞的表型。本文描述了首个可在单一细胞类型(NK 细胞)上潜在共表达 35 个标记的光谱流式细胞术 panel,包括 panel 设计过程、样本制备、染色方案、质量控制指标、采集方案以及分析外周和肝脏 NK 细胞的工作流程。通过纳入分化、成熟、组织驻留、迁移潜能、功能状态、关键转录因子和免疫检查点分子的标记,可区分 NK 细胞亚群和表型。通过纳入额外标记并修改已发表的设门策略,可鉴定肝脏 I 型固有淋巴细胞(Lt-ILC1s)。
此外,我们描述了外周和肝脏NK细胞的动态变化。最后,我们展示了所纳入的标志物在肝细胞癌(HCC)患者样本中指示NK细胞功能障碍的有效性。这一高参数高分辨率panel为深入描绘外周和肝脏中不同NK细胞亚群在健康和疾病状态下的特征提供了关键工具。它能够稳健地识别低频率的NK细胞亚群,并可有效用于细胞数量有限的样本。
Natural killer cells (NK cells) are granular lymphocytes with cytotoxic activity that have a role in both innate and adaptive immune responses. NK cells consist of a diverse array of phenotypes with specific functions imposed by the microenvironment. Liver NK cells are an abundant lymphocyte population playing a key role in tuning immune responses under physiological and pathological conditions. For example, NK cell functional and phenotypic changes occur during liver cancer progression and correlate with disease prognosis.
As liver cancer has the second-highest mortality rate among solid cancers, it is important to define the composition and the dynamics of the liver and peripheral NK cell compartment both in health and disease state. In-depth analysis of the phenotypes and functional status of NK cells and their frequencies will expand our knowledge on their role in maintaining immune tolerance, disease progression, and aid the development of novel treatments.
We present here a 41-marker 37-color spectral flow cytometry panel for the in-depth phenotyping of human peripheral and liver NK cells. This paper describes the first spectral flow cytometry panel with 35 markers potentially co-expressed on one cell type (NK cells) including the panel design process, sample preparation, staining protocol, quality control metrics, acquisition protocol and workflows to analyze NK cells in the periphery and liver.
NK cell subsets and phenotypes were distinguished by including markers of differentiation, maturation, tissue residency, migratory potential, functional status, key transcription factors, and immune checkpoint molecules. Liver-type ILC1s (Lt-ILC1s) could be identified by inclusion of additional markers and modification of published gating strategies.
Furthermore, we describe the dynamics of peripheral and liver NK cells.
Finally, we show the validity of markers included to indicate NK cell dysfunction in samples of patients with Hepatocellular Carcinoma (HCC). This high parameter high resolution panel provides a key tool for in-depth delineation of distinct NK cell subsets in the periphery and in liver, in health and disease state. It allows for the robust identification of NK cells subsets with low frequencies and can effectively be used for samples with limited cell numbers.
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