neutrophil phagocytosis assay

用于筛选不同信号通路的中性粒细胞功能检测

Neutrophils are the most abundant innate immune cells in human blood and are known to play a major part in infection and inflammation, being the first responders to arrive at the site of tissue damage1. In recent years, there has been a growing recognition of the crucial role that neutrophils play in a variety of diseases and in supporting homeostasis2. Neutrophils not only have tightly regulated signaling themselves, but also participate in the regulation of other components of the immune system3,4,5. Therefore, investigating neutrophils and their many unusual cellular functions, such as chemotaxis, reverse migration6, phagocytosis7, respiratory burst8, and the release of neutrophil extracellular traps (NETs)7, is imperative in numerous research contexts where it is necessary to assess the potential neutrophil functional, morphological, or molecular changes triggered by specific conditions under analysis.
Freshly isolated neutrophils are terminally differentiated, short-lived, highly dynamic, and easily activated9. However, an efficient storage method that does not affect the neutrophil responses has not yet been achieved, making it challenging to perform multiple assays that must be uninterrupted. Furthermore, previously described functional analyses10,11, based on assays that require cytometry and/or fluorescent staining, may not be a viable choice when a broad and initial evaluation of the neutrophil is needed.
To address these issues, this protocol describes a set of tests that can be carried out following a single isolation process, including the evaluation of cell viability, reactive oxygen species (ROS) production, real-time migration, and phagocytosis of Saccharomyces cerevisiae, whose results can be used to reason in-depth follow-up studies. This procedure, named NeutroFun Screen, was designed to encompass the leading effector activities, except degranulation, and can be completed in an average time of 4 h, including 1 h of activation. Additionally, the remaining cells can be used for more detailed approaches like omics studies. The advantage of this method lies in its balance between speed, comprehensiveness, cost, and accuracy.
Furthermore, there is a way to easily observe a preliminary suggestion of NETs, without specific markers, but enough to indicate if further efforts in that direction would be worthwhile. The diversity of functions tested aims to combine common points among tests, reducing the analysis time and expenses. The main goal of this method is to provide a balanced, functional analysis regarding speed, comprehensiveness, cost, and accuracy that allows for an overview of the neutrophil&#39;s response, making it a useful initial step in investigating the effects of novel stimuli on normal density neutrophils.

作者聚焦：使用 NeutroFun 筛选方案平衡中性粒细胞功能评估的速度、成本和准确性 

一套快速了解中性粒细胞功能的筛查技术

Watch this Scientific Journal Video about Neutrophil Phagocytosis Assay at JoVE.com

中性粒细胞吞噬作用测定

将约0.75毫克干酵母加入200微升含有钙和镁离子的Hanks平衡盐溶液（HBSS）中。接下来，将混合物在 100 摄氏度和 500 转/分的 ThermoMixer 中孵育至少 15 分钟。孵育后，将5微升酵母悬浮液转移到45微升0.2%台盼蓝染料中。使用Neubauer室对酵母细胞进行计数。使用含有钙和镁的HBSS将初始悬浮液的浓度调节至每微升33,000个酵母细胞。接下来，在新的无菌微量离心管中，轻轻地混合并转移五微升先前制备的活化多形核中性粒细胞与五微升酵母细胞悬浮液。立即将6微升多形核中性粒细胞和酵母悬浮液转移到干净载玻片的三个孔中，每个孔2微升，并将载玻片在加湿室中孵育40分钟。用快速全景染色后，在显微镜下观察细胞。尽管 100 纳摩尔 FMLP 和 16 微摩尔抗菌肽都诱导了酵母吞噬的增加，但在双重刺激之前，差异没有统计学意义，与对照组相比，这显着增强了吞噬作用。

Research

JoVE Journal

Immunology and Infection

Neutrophil Phagocytosis Assay

228 次观看. 将约0.75毫克干酵母加入200微升含有钙和镁离子的Hanks平衡盐溶液（HBSS）中。接下来，将混合物在 100 摄氏度和 500 转/分的 ThermoMixer 中孵育至少 15 分钟。孵育后，将5微升酵母悬浮液转移到45微升0.2%台盼蓝染料中。使用Neubauer室对酵母细胞进行计数。使用含有钙和镁的HBSS将初始悬浮液的浓度调节至每微升33,000个酵母细胞。接下来，在新的无菌微量离心管中，轻轻地混合并?...

视频: 中性粒细胞吞噬作用测定

A Set of Screening Techniques for a Quick Overview of the Neutrophil Function

Neutrophils are known as one of the first lines of defense in the innate immune response and can perform many particular cellular functions, such as chemotaxis, reverse migration, phagocytosis, degranulation of cytotoxic enzymes and metabolites, and release of DNA as neutrophil extracellular traps (NETs). Neutrophils not only have tightly regulated signaling themselves, but also participate in the regulation of other components of the immune system. As fresh neutrophils are terminally differentiated, short-lived, and highly variable among individuals, it is important to make the most of the collected samples. Researchers often need to perform screening assays to assess an overview of the many neutrophil functions that may be affected by specific conditions under evaluation. A set of tests following a single isolation process of normal density neutrophils was developed to address this need, seeking a balance between speed, comprehensiveness, cost, and accuracy. The results can be used to reason and guide in-depth follow-up studies. This procedure can be carried out in an average time of 4 h and includes the evaluation of cell viability, reactive oxygen species (ROS) production, real-time migration, and phagocytosis of yeast on glass slides, leaving enough cells for more detailed approaches like omics studies. Moreover, the procedure includes a way to easily observe a preliminary suggestion of NETs after fast panoptic staining observed by light microscopy, with a lack of specific markers, albeit enough to indicate if further efforts in that way would be worthwhile. The diversity of functions tested combines common points among tests, reducing the analysis time and expenses. The procedure was named NeutroFun Screen, and although having&#160;limitations, it balances the aforementioned factors. Furthermore, the aim of this work is not a definite test set, but rather a guideline that can easily be adjusted to each lab&#39;s resources and demands.

This protocol features a set of neutrophil functional assays to be used as a screening method to cover functions from different signaling pathways. The protocol includes an initial and simple evaluation of cell viability, purity, reactive oxygen species production, real-time migration, phagocytosis, and a preliminary suggestion of neutrophil extracellular traps.

Neutrophils are known as one of the first lines of defense in the innate immune response and can perform many particular cellular functions, such as ...