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加勒8针对受损的囊泡进行自,以防御细胞免受细菌入侵
Teresa L M Thurston1, Michal P Wandel, Natalia von Muhlinen
1MRC Laboratory of Molecular Biology, Division of Protein and Nucleic Acid Chemistry, Hills Road, Cambridge CB2 0QH, UK.
Nature
|January 17, 2012
概括
盖莱克8作为细胞质危险受体,通过检测细胞囊泡的损伤来识别像沙门氏菌这样的入侵细菌. 这就启动了细胞防御机制自,以消除病原体.
科学领域:
- 细胞生物学 细胞生物学
- 免疫学 免疫学 免疫学
- 微生物学 微生物学
背景情况:
- 自是细胞对抗细菌入侵的关键防御机制.
- 自适配器需要模式识别或危险受体来识别病原体.
- 参与标记自病原体的特定受体仍然在很大程度上未被确定.
研究的目的:
- 确定负责启动抗菌自的特定危险受体.
- 阐明这种受体检测和信号细菌入侵的机制.
- 确定这种受体在限制病原体扩散中的作用.
主要方法:
- 人类细胞培养的人类细胞培养
- 同焦点显微镜的共聚焦显微镜
- 免疫光测定试验
- 细菌感染模型 (沙门氏菌,李斯特菌,西格拉菌)
主要成果:
- 加列8 (LGALS8) 作为细胞质危险受体起作用.
- 加勒8通过将宿主甘氨酸结合到损坏的含沙门氏菌的真空体上来检测细菌入侵.
- 盖莱克8招募NDP52 (CALCOCO2),激活抗菌自.
- 加列8还可以检测内分体/溶解体的无菌损伤以及李斯特菌和西格拉菌的入侵.
结论:
- 加勒8是一种多功能危险受体,可监测内体和 lysosomal 完整性.
- 它通过启动自而对抗细胞内细菌感染起着至关重要的作用.
- 这种机制依赖于检测细胞质中缺乏复杂碳水化合物,表明损伤或入侵.
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