HMGB1的功能是作为在肠道粘膜屏障中宿主防御的关键调解者
Anne-Marie C Overstreet1, McKenzie Burge1, Brady Anderson1
1Department of Microbial Sciences in Health, Cleveland Clinic Research, Cleveland Clinic, Cleveland, OH 44195, USA.
Cell host & microbe
|February 4, 2026
概括
高流动性组盒1 (HMGB1) 结合肠道中的细菌蛋白 (ToH1),防止入侵. 这种相互作用在性结肠炎中被破坏,突出显示ToH1是新的抗菌策略的潜在目标.
科学领域:
- 微生物学 微生物学
- 免疫学 免疫学 免疫学
- 胃肠病学 胃肠病学
背景情况:
- 主体细胞和肠道细菌通过粘膜屏障相互作用,但分子机制尚不清楚.
- 高流动性组盒1 (HMGB1) 在对微生物群的反应中释放到结肠粘液中.
研究的目的:
- 为了阐明HMGB1和细菌之间的分子反循环.
- 研究HMGB1 (ToH1) 序列的标在细菌与宿主相互作用和疾病中的作用.
主要方法:
- 研究了HMGB1与含有ToH1序列的细菌表面蛋白结合.
- 分析了细菌聚合,粘膜入侵和粘附.
- 在开始性和致病性细菌中检查了ToH1的表达.
- 在性结肠炎模型中评估HMGB1和ToH1水平.
主要成果:
- HMGB1与含有ToH1的细菌蛋白质结合,促进聚合并限制侵入/粘附.
- 在遇到HMGB1.1时,共生细菌会降低ToH1粘附蛋白的调节.
- 性结肠炎显示HMGB1防御受损,并丰富了ToH1阳性附着细菌.
- ToH1被广泛使用,对毒性至关重要,并且表达不同.
结论:
- 在HMGB1通过ToH1.1限制细菌粘膜相互作用的地方存在反循环.
- 在性结肠炎中,HMGB1防御受损与附着细菌增加有关.
- ToH1是微生物毒性决定因素,也是新型抗菌疗法的潜在目标.
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