发布: 2017年04月05日第7卷第7期 DOI: 10.21769/BioProtoc.2213 浏览次数: 9956
评审: Alka MehraSaskia F. ErttmannSadri Znaidi
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在活细胞成像中测量趋化因子刺激下Jurkat细胞的Piezo1和肌动蛋白极性
Chinky Shiu Chen Liu [...] Dipyaman Ganguly
2024年10月05日 1081 阅读
Abstract
In this protocol we describe how to visualize neutrophil extracellular traps (NETs) and fungal cell wall changes in the context of the coculture of mouse neutrophils with fungal hyphae of Candida albicans. These protocols are easily adjusted to test a wide array of hypotheses related to the impact of immune cells on fungi and the cell wall, making them promising tools for exploring host-pathogen interactions during fungal infection.
Keywords: Fungi (真菌)Background
C. albicans is a polymorphic opportunistic yeast and neutrophils are immune cells critical for defense against this and other fungal pathogens (Brown et al., 2012; Lionakis and Netea, 2013). NETs are a potential defense mechanism that can be deployed against pathogens and it has been suggested that they are preferentially deployed against microbial cells such as C. albicans hyphae that are too large to phagocytose (Urban et al., 2006; Bruns et al., 2010; Branzk et al., 2014; Rohm et al., 2014). NETs have been shown to contain a number of components including myeloperoxidase, extracellular DNA and citrullinated histones (Amulic et al., 2012; Branzk and Papayannopoulos, 2013). For positive identification of NETs, the standard in both in vitro and in vivo experiments includes staining for and demonstrating the colocalization of these markers. While the exact contribution of NETs to defense against C. albicans infection is not well understood, our group has demonstrated they can provoke stress responses and cell wall rearrangement in C. albicans hyphae. Specifically, NET attack results in greater chitin deposition and β-glucan exposure as shown schematically in Figure 1. These polysaccharides normally lie underneath the mannan layer, and their exposure can change immune recognition (Perez-Garcia et al., 2011). The basic assays described here were used extensively to probe this subject by our group (Hopke et al., 2016). While outlined here for the purpose of detecting NETs and fungal cell wall changes, this protocol is easily tweaked to leverage many combinations of chemical inhibitors, transgenic or knockout fungal strains or mouse neutrophils and other staining targets to test a wide array of hypotheses (Hopke et al., 2016). This protocol therefore represents a promising method to further elucidate the impact immune cells have on the C. albicans cell wall, its stress response and the importance of altered epitope exposure to host defense against fungal infection.
Figure 1. Schematic of cell wall organization pre- and post-neutrophil attack. Under homeostatic conditions, hyphal cell wall is composed of three main polysaccharide components (mannan, β-glucan and chitin) but most chitin and β-glucan are inaccessible for recognition because it lies beneath the mannan layer. Post-attack there is loss of cell wall mannoprotein and increased levels of chitin. These changes lead to greater surface recognition of β-glucan and perhaps also chitin.
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版权信息
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Readers should cite both the Bio-protocol article and the original research article where this protocol was used:
分类
免疫学 > 免疫细胞成像 > 共聚焦显微镜技术
微生物学 > 微生物-宿主相互作用 > 真菌
细胞生物学 > 细胞染色 > 细胞壁
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