发布: 2017年08月20日第7卷第16期 DOI: 10.21769/BioProtoc.2509 浏览次数: 7452
评审: Anonymous reviewer(s)
Abstract
Macrophages maintain tissue homoeostasis by regulating inflammation and tissue repair mechanisms. Thus, the fate of macrophages has an impact on the state of the tissue. The aim of this protocol is to quantify macrophage survival using high content microscopy and image processing software. Here, we describe a high-content image based protocol to assess the effect of diverse stimuli in combination with pharmacological treatments on macrophage survival in a quantitative, unbiased and high-throughput manner.
Keywords: Macrophage (巨噬细胞)Background
Macrophages are phagocytic innate immune cells and are the main drivers of inflammation in tissue (Medzhitov, 2008). These cells are associated with cancer together with autoimmune, autoinflammatory, infectious, neurodegenerative and metabolic diseases (Ginhoux and Jung, 2014). In this context, the role of macrophages in inflammation is well-studied, however, the impact of macrophage survival in non-infectious and infectious diseases is largely unknown. Our study showed that the activation of certain pathogen-associated receptors (PRRs) can induce macrophage survival (Eren et al., 2016). We described a molecular mechanism that demonstrated how an obligate intracellular pathogen exploits PRR-induced cell survival (Eren et al., 2016). Thus, further studies are necessary to understand the role of macrophage survival in different disease settings.
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文章信息
版权信息
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Eren, R. and Fasel, N. (2017). Macrophage Survival Assay Using High Content Microscopy. Bio-protocol 7(16): e2509. DOI: 10.21769/BioProtoc.2509.
分类
免疫学 > 免疫细胞成像 > 高内涵显微镜技术
细胞生物学 > 细胞成像 > 荧光
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