
Toll-like receptor - Wikipedia
Toll-like receptors (TLRs) are a class of proteins that play a key role in the innate immune system. They are single-spanning receptors usually expressed on sentinel cells such as macrophages …
TLR4——细菌LPS的受体 - 知乎 - 知乎专栏
Toll 样受体 4 (Toll-like receptor 4,TLR4)是由 Poltorak 等于 1998 年发现的 一种 I 型跨膜蛋白,其由 TLR4 基因编码,并表达于包括单核细胞,巨嗜细胞在内 的多种组织细胞中,可以识 …
LPS/TLR4 signal transduction pathway - PubMed
The stimulation of Toll-like receptor 4 (TLR4) by lipopolysaccharide (LPS) induces the release of critical proinflammatory cytokines that are necessary to activate potent immune responses. …
Toll样受体的类型、定位与功能 - 知乎 - 知乎专栏
2024年1月22日 · 以下是tlr4的几个关键功能:识别lps: tlr4与共受体md-2结合,形成一个复合体,可以有效地识别和结合lps。 信号传导: 识别LPS后,TLR4复合体通过两种不同的途径传递 …
Recognition of lipopolysaccharide pattern by TLR4 complexes
2013年12月6日 · In this review, we summarize these structures and describe the structural basis of LPS recognition by LPS receptors and accessory proteins. In the initial phase of infection, …
Signal transduction by the lipopolysaccharide receptor, Toll-like ...
TLR4 has now been established as the receptor for LPS; however, in addition to this, TLR4 also recognizes lipoteichoic acid (LTA), fibronectin, the fusion protein of respiratory syncytial virus …
Toll-like Receptor-4 Mediates Lipopolysaccharide-induced Signal ...
1999年4月16日 · TLR4 is a member of the recently identified Toll-like receptor family of proteins and has been putatively identified as Lps, the gene necessary for potent responses to …
LPS/TLR4 Signal Transduction Pathway - CUSABIO
TLRs are important receptors involved in innate immunity, and they can specifically identify and combine pathogen-associated molecular patterns (PAMPs), triggering a series of signal …
免疫机制的多样性与TLR4在LPS识别中的关键作用|细胞|蛋白|介导|lps|tlr…
1978年,James Watson首次提出小鼠体内可能存在控制LPS反应的特定基因,取名为Lps,认为该基因可能有两个等位基因:即Lpsd(defective response〉和Lpsn(normal response)。三 …
Toll-like receptor 2 is required for LPS-induced Toll-like receptor …
2012年6月8日 · TLR2 plays a dual role in the induction of intracellular signals that impair MTAL function, both through cooperation with TLR4 to mediate ERK signaling by LPS and through a …