SFTSV使用AXL/GAS6通过PI3K-PLC-依赖的AXL-激酶激活的巨细胞
Zecheng Jin1,2,3, Shuhei Taguwa1,2,3, Junki Hirano1,2
1Center for Infectious Disease Education and Research (CiDER), Osaka University, Osaka, Japan.
Journal of virology
|August 25, 2025
概括
严重发烧与血小板缩小综合征病毒 (SFTSV) 使用AXL,一个受体激素酶,进入细胞. 这一发现揭示了SFTSV感染的新途径,并将AXL作为潜在的治疗点.
科学领域:
- 病毒学
- 细胞生物学
- 分子医学
背景情况:
- 严重发烧与血小板缺血综合征 (SFTS) 是由SFTS病毒 (SFTSV) 引起的严重公共卫生问题.
- 之前的研究确定了DC-SIGN和C型讲蛋白为SFTSV受体,但完全的进入机制仍然不清楚.
研究的目的:
- 确定SFTSV的新细胞受体和进入途径.
- 探索SFTSV感染的潜在治疗点.
主要方法:
- 全基因组的CRISPR激活查以识别SFTSV进入受体.
- 研究AXL,增长停止特异性蛋白6和PLC在SFTSV输入中的作用.
- 使用各种细胞类型的SFTSV感染模型,包括HUVEC.
主要成果:
- 一个受体氨酸激酶 (AXL) 被确定为一种新的SFTSV入口受体.
- 通过 AXL 进入 SFTSV 涉及增长停止特异性蛋白 6,导致 PI3K 和 PLC 招募.
- 这种相互作用触发了SFTSV进入的宏细胞路径,在多种细胞类型中得到证实.
结论:
- AXL通过PI3K/PLC依赖的巨细胞路径调解SFTSV的进入.
- 这种途径与以前已知的病毒进入机制不同.
- 在开发新型抗SFTSV策略方面,AXL是一个有前途的治疗标.
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