Li Yaoming, Liu Fang, Han Chen, Yan Huimin
State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, Hubei, People's Republic of China.
Hybridoma (Larchmt). 2012 Feb;31(1):60-2. doi: 10.1089/hyb.2011.0083.
The conserved domain of bacteria-derived flagellin coupling Toll-like receptor 5 (TLR5) activates NF-κB and MAPK signaling transductions, which subsequently regulate the transcription and expression of genes encoding immune mediators. However, whether the flagellin binding monoclonal antibody (MAb) obstructs TLR5-associated signaling is unclear. Here we report on the production and characterization of MAb 5G10 that specifically recognizes flagellin. The MAb 5G10 was produced by the hybridization of mouse myeloma cell SP2/0 with splenocyte from a flagellin immunized BALB/c mouse. We observed that deletion of the conserved amino acid residues 89-96 made flagellin lose its capacity for binding 5G10. Additionally, MAb 5G10 remarkably suppressed the expression of cytokine IL8 of Caco-2 cell by blocking the flagellin-TLR5 signaling. Furthermore, this MAb would be useful for cytosolic localization of flagellin and would facilitate the elucidation of the physiological function of specific pathogen-associated molecular patterns.
源自细菌的鞭毛蛋白的保守结构域与Toll样受体5(TLR5)结合,激活核因子κB(NF-κB)和丝裂原活化蛋白激酶(MAPK)信号转导,随后调节编码免疫介质的基因的转录和表达。然而,鞭毛蛋白结合单克隆抗体(MAb)是否会阻碍TLR5相关信号尚不清楚。在此,我们报道了特异性识别鞭毛蛋白的单克隆抗体5G10的制备及特性。单克隆抗体5G10是通过将小鼠骨髓瘤细胞SP2/0与经鞭毛蛋白免疫的BALB/c小鼠的脾细胞杂交产生的。我们观察到,保守氨基酸残基89-96的缺失使鞭毛蛋白失去了与5G10结合的能力。此外,单克隆抗体5G10通过阻断鞭毛蛋白-TLR5信号,显著抑制了Caco-2细胞中细胞因子IL8的表达。此外,该单克隆抗体可用于鞭毛蛋白的胞质定位,并有助于阐明特定病原体相关分子模式的生理功能。