生物
巨噬细胞
免疫组织化学
人口
免疫学
表型
炎症
病理
细胞生物学
基因
医学
遗传学
体外
环境卫生
作者
Stephen Huang,Dylan Carter‐Cusack,Emma Maxwell,Omkar L. Patkar,Katharine M. Irvine,David Hume
出处
期刊:Methods in molecular biology
日期:2023-08-28
卷期号:: 99-115
被引量:1
标识
DOI:10.1007/978-1-0716-3437-0_6
摘要
Macrophages contribute to many aspects of development and homeostasis, innate and acquired immunity, immunopathology, and tissue repair. Every tissue contains an abundant resident macrophage population. Inflammatory stimuli promote the recruitment of monocytes from the blood and their adaptation promotes the removal of the stimulus and subsequent restoration of normal tissue architecture. Dysregulation of this response leads to chronic inflammation and tissue injury. In many tissues, their differentiation and survival are dependent on the colony stimulating factor 1 receptor (CSF1R) signalling axis, which is highly conserved across all vertebrates. Complete loss of either CSF1R or its cognate ligands, colony stimulating factor 1 (CSF1), and interleukin 34 (IL-34), results in the loss of many tissue-resident macrophage populations. This provides a useful paradigm to study macrophages. There are many tools used to visualize tissue-resident macrophagesTissue resident macrophages and their precursors, monocytes, in mice and humans. Particularly in mice there are genetic tools available to delete, enhance and manipulate monocytes and macrophages and their gene products to gain insight into phenotype and function. The laboratory rat has many advantages as an experimental model for the understanding of human disease, but the analytical resources are currently more limited than in mice. Here, we describe available genetic models, antibodiesAntibodies, and immunohistochemistry (IHC) methods that may be used to visualize tissue-resident macrophagesTissue resident macrophages in rats.
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