neutrophil phagocytosis assay

Farklı Sinyal Yollarının Tizlenmesi için Nötrofil Fonksiyonel Tahliller

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.

Yazar Spotlight: NeutroFun Ekran Protokolü ile Nötrofil Fonksiyon Değerlendirmesinde Hız, Maliyet ve Doğruluğun Dengelenmesi 

Nötrofil fonksiyonuna hızlı bir genel bakış için bir dizi tarama tekniği

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

Nötrofil Fagositoz Testi

Kalsiyum ve magnezyum iyonları içeren 200 mikrolitre Hanks' Dengeli Tuz Çözeltisine veya HBSS'ye yaklaşık 0.75 miligram kuru maya ekleyin. Ardından, karışımı bir ThermoMixer'da 100 santigrat derece ve 500 rpm'de en az 15 dakika inkübe edin. İnkübasyondan sonra, beş mikrolitre maya süspansiyonunu 45 mikrolitre% 0.2 Tripan mavi boyaya aktarın.Bir Neubauer odası kullanarak maya hücrelerini sayın. Kalsiyum ve magnezyum içeren HBSS kullanarak ilk süspansiyonun konsantrasyonunu mikrolitre başına 33.000 maya hücresine ayarlayın. Daha sonra, önceden hazırlanmış aktive edilmiş polimorfonükleer nötrofillerin beş mikrolitresini yeni, steril bir mikrosantrifüj tüpünde maya hücresi süspansiyonunun beş mikrolitresine hafifçe karıştırın ve aktarın.Hemen altı mikrolitre polimorfonükleer nötrofiller ve maya süspansiyonunu, her biri iki mikrolitre olmak üzere temiz bir cam slaytın üç kuyusuna aktarın ve slaytı nemlendirilmiş bir odada 40 dakika inkübe edin. Hızlı panoptik ile boyadıktan sonra, mikroskop altında hücreleri gözlemleyin. Hem 100 nanomolar FMLP hem de 16-mikromolar antimikrobiyal peptit, artmış bir maya yutulmasına neden olmasına rağmen, kontrol grubuna kıyasla fagositozu önemli ölçüde artıran ikili stimülasyona kadar fark istatistiksel olarak anlamlı değildi.

Research

JoVE Journal

Immunology and Infection

Neutrophil Phagocytosis Assay

231 Görüntüleme. Kalsiyum ve magnezyum iyonları içeren 200 mikrolitre Hanks' Dengeli Tuz Çözeltisine veya HBSS'ye yaklaşık 0.75 miligram kuru maya ekleyin. Ardından, karışımı bir ThermoMixer'da 100 santigrat derece ve 500 rpm'de en az 15 dakika inkübe edin. İnkübasyondan sonra, beş mikrolitre maya süspansiyonunu 45 mikrolitre% 0.2 Tripan mavi boyaya aktarın.Bir Neubauer odası kullanarak maya hücrelerini sayın. Kalsiyum ve magnezyum içeren HBSS kullanarak ilk süspansiyonun konsantr...

Video: Nötrofil Fagositoz Testi

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 ...