TLR4型
化学
细胞生物学
Toll样受体
MAPK/ERK通路
流式细胞术
分泌物
巨噬细胞
信号转导
磷酸化
CD86
基因敲除
受体
分子生物学
先天免疫系统
生物化学
生物
体外
细胞凋亡
基因
表型
作者
Yang Yi,Xiaoliang Zhao,Jia Li,Hao Jiang,Xindi Shan,Ya Wang,Wenbang Ma,Jiejie Hao,Guangli Yu
标识
DOI:10.1016/j.carbpol.2018.03.019
摘要
We studied the mechanisms underlying the immunostimulatory effects of aβ-1,3/1,6-glucan (BG136) from Durvillaea Antarctica. Our data showed that BG136 promoted the activation of MAPKs and NF-κB signaling pathways and cytokines production. BG136 did not increase MCP-1 or NO production or phosphorylation of NF-κB and MAPK in TLR4 siRNA knockdown cells, indicating that BG136 activates macrophages through TLR4. Flow cytometry analysis and confocal experiment showed that BG136 bound to TLR4 expressed on RAW264.7 macrophage cells surface. The affinity of BG136 for TLR4 was determined using Surface Plasmon Resonance (SPR) (KD: 4.51 × 10−6M). Altogether, our results showed that BG136 activates RAW264.7 cells by binding to TLR4 and then triggering TLR4-mediated signaling pathways to promote cytokines secretion.
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