S100A9与CD14上的一个动态区域相互作用,激活Toll类受体4
bioRxiv : the preprint server for biology
|May 27, 2024
概括
与损伤相关的分子模式S100A9通过膜结合的CD14激活了Toll-like受体4. 这种相互作用涉及CD14内部化,并为S100A9诱导的炎症提供了分子洞察力.
科学领域:
- 免疫学 免疫学 免疫学
- 分子生物学分子生物学
背景情况:
- 损伤相关分子模式 (DAMP) 的S100A9通过托尔类受体4 (TLR4) 触发炎症反应.
- 虽然对于组织修复至关重要,但S100A9在炎症疾病中的作用需要了解其激活机制.
- CD14已被确定为S100A9介导的TLR4激活所必需的共同受体.
结论:
- 这些发现表明,S100A9通过CD14依赖的受体复合体内化激活TLR4.
- 分子表征显示S100A9与CD14的动态N端区域结合,适应可溶性蛋白质和LPS等小分子.
- 这项研究为S100A9 / CD14相互作用提供了第一个分子洞察力,促进了对S100A9介导的TLR4激活的理解.
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