发布: 2019年09月20日第9卷第18期 DOI: 10.21769/BioProtoc.3369 浏览次数: 4531
评审: Alka MehraMartin V KolevMarieta Ruseva

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Abstract
Internalization of cell surface Toll-like Receptor 4 (TLR4) is a convenient read-out to measure LPS dependent activation of the TRIF adaptor pathway. We here provide a protocol to quantify the LPS dependent internalization of TLR4 using thioglycollate-elicited peritoneal macrophages by flow cytometry.
Keywords: TLR4 (Toll样受体4)Background
Toll-like Receptor 4 (TLR4) is unique among the Toll-like receptors in that it can deliver qualitatively different signals from two distinct cellular locations (reviewed in Takeda and Akira, 2004). Cell surface TLR4/MD2 is initially ligated by extracellular bacterial lipopolysaccharide (LPS) and engages the intracellular adaptor MAL and MyD88. Subsequently a fraction of cell surface LPS bound TLR4/MD2 will undergo CD14 and clathrin dependent internalization and translocation to an early endosomal compartment (Zanoni et al., 2011). In this endosomal compartment TLR4, engages the signaling adaptors TRAM and TRIF. Much of the regulation of TLR4 internalization and transport remains to be discovered. A flow cytometric method for quantifying loss of TLR4 surface expression, as a metric for endosomal translocation was first described in Bone Marrow Derived Macrophages (BMDMs) by Jonathan Kagan and colleagues (Kagan et al., 2008). Here we describe a modified version of this protocol to enable quantitation of TLR4 internalization in thioglycollate-elicited peritoneal macrophages on which we have published (Rajaiah et al., 2015; Perkins et al., 2018).
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版权信息
© 2019 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Richard, K., Vogel, S. N. and Perkins, D. (2019). Quantitation of TLR4 Internalization in Response to LPS in Thioglycollate Elicited Peritoneal Mouse Macrophages by Flow Cytometry. Bio-protocol 9(18): e3369. DOI: 10.21769/BioProtoc.3369.
分类
细胞生物学 > 基于细胞的分析方法 > 流式细胞术
免疫学 > 免疫细胞功能 > 巨噬细胞
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