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用影像流式细胞仪评估人单核细胞中经典炎症小体的激活。

Evaluation of Canonical Inflammasome Activation in Human Monocytes by Imaging Flow Cytometry.

机构信息

National Institute of Allergy and Infectious Diseases, Bethesda, MD, United States.

Flow Cytometry Core Facility, National Heart, Lung, and Blood Institute, Bethesda, MD, United States.

出版信息

Front Immunol. 2019 Jun 4;10:1284. doi: 10.3389/fimmu.2019.01284. eCollection 2019.

Abstract

Canonical inflammasome activation is a tightly regulated process that has been implicated in a broad spectrum of inflammatory disorders. Inflammasome formation requires assembly of a cytosolic sensor protein with the adapter, ASC (apoptosis-associated speck-like protein containing a caspase activating and recruitment domain). Once formed, this multimeric protein structure allows for the activation of caspase-1, responsible for IL-1ß/IL-18 release. During this process, cytoplasmic dispersed ASC molecules cluster in one condensed micrometric-sized complex named ASC "speck," which is traditionally assessed by fluorescence microscopy and widely accepted as a readout for canonical inflammasome activation. However, equally reliable but less time-consuming quantitative methods have emerged as a significant need in order to improve clinical assessment of inflammasome-related conditions. Multispectral imaging flow cytometry (MIFC) combines the qualitative power of fluorescence microscopy with high throughput capabilities and multiplexing potential of flow cytometry into one single system. Here we explored the optimal imaging-based tools to measure ASC speck formation via imaging flow cytometry by using peripheral blood mononuclear cells (PBMCs) stimulated with the NLRP3 agonist Nigericin, as a positive control. We demonstrate that this technique is also able to detect the distribution of active caspase-1 within the ASC aggregates by incubating cells with FAM-FLICA, a fluorochrome inhibitor of caspase-1. By applying these tools in PBMCs from patients with distinct inflammatory disorders we demonstrate that MIFC is able to assess canonical inflammasome activation in a quantitative and statistically robust manner in clinically relevant samples. Therefore, we propose that accurate assessment of specks by MIFC could help guide preventive or therapeutic strategies in an array of human inflammatory diseases in which inflammasomes play an important role.

摘要

经典的炎性小体激活是一个受到严密调控的过程,它与广泛的炎症性疾病有关。炎性小体的形成需要胞质传感器蛋白与衔接蛋白 ASC(含半胱天冬酶募集结构域的凋亡相关斑点样蛋白)组装。一旦形成,这种多聚体蛋白结构允许半胱天冬酶-1的激活,负责白细胞介素-1β/白细胞介素-18 的释放。在这个过程中,细胞质中分散的 ASC 分子在一个凝聚的微毫米大小的复合物中聚集,称为 ASC“斑点”,传统上通过荧光显微镜评估,并且被广泛认为是经典炎性小体激活的读出。然而,同样可靠但耗时更少的定量方法已经成为一种重要的需求,以改善对炎性小体相关疾病的临床评估。多光谱成像流式细胞术(MIFC)将荧光显微镜的定性能力与高通量能力以及流式细胞术的多重分析潜力结合在一个单一的系统中。在这里,我们通过使用 NLRP3 激动剂 Nigericin 刺激外周血单核细胞(PBMCs)作为阳性对照,探索了通过成像流式细胞术测量 ASC 斑点形成的最佳基于成像的工具。我们证明,通过用 FAM-FLICA(一种半胱天冬酶-1 的荧光抑制剂)孵育细胞,该技术也能够检测到 ASC 聚集体中活性半胱天冬酶-1 的分布。通过将这些工具应用于来自具有不同炎症性疾病的患者的 PBMCs,我们证明 MIFC 能够以定量和统计学上稳健的方式评估临床相关样本中的经典炎性小体激活。因此,我们提出,MIFC 对斑点的准确评估可以帮助指导在炎症小体发挥重要作用的一系列人类炎症性疾病中的预防或治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/6558012/b83b2aab0512/fimmu-10-01284-g0001.jpg

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