暴露于寒冷会增加通过细胞外冷诱导性RNA结合蛋白和类似受体4信号的收费增加大动脉剖析风险
Hsiao-Ya Tsai1, Wu-Chien Chien2,3,4, Chi-Hsiang Chung2,3,4
1Department of Emergency Medicine, Tri-Service General Hospital, National Defense Medical University, No. 325, Sec. 2, Cheng-Kung Road, Neihu District, Taipei City, 114, Taiwan.
Scientific reports
|March 11, 2026
概括
寒冷的天气增加了大动脉解剖 (AD) 的风险. 寒冷压力和细胞外冷诱导性RNA结合蛋白 (eCIRP) 通过激活托尔类受体4 (TLR4) 途径,使AD恶化. 阻止eCIRP是一种潜在的治疗方法.
科学领域:
- 心血管研究研究心血管研究
- 免疫学 免疫学 免疫学
- 环境健康 环境健康
背景情况:
- 观察性研究将寒冷的天气与心血管疾病风险增加联系起来.
- 冷诱导型RNA结合蛋白 (CIRP) 具有保护作用,但细胞外CIRP (eCIRP) 作为危险信号触发炎症.
- 了解寒冷压力对血管健康的影响对于预防紧急情况至关重要.
研究的目的:
- 为了研究低温与大动脉剖析 (AD) 发展之间的关联.
- 阐明将寒冷压力与血管细胞损伤联系在一起的机制.
- 探索eCIRP作为感冒引起的血管紧急情况的治疗目标.
主要方法:
- 分析气象数据和医疗保险索赔,以将低温与AD相关联.
- 使用3-aminopropionitrile fumarate (BAPN) 和急性寒冷暴露 (ACE) 建立一种小鼠AD模型.
- 在体外对内皮细胞的研究和在体内对CIRP抗剂的实验.
主要成果:
- 寒冷压力和ecirp诱导了血管炎症和通过托尔类受体4 (TLR4) 途径的矩阵金属蛋白酶-2过度表达.
- 在较低的温度下观察到AD的发病率更高.
- 在接受BAPN治疗的小鼠中,ACE加剧了AD,增加了大动脉直径和炎症标志物;C23,一种CIRP对手,显示出保护作用.
结论:
- 低温与AD的发展有关,特别是在特定的气候条件下.
- 细胞外CIRP (eCIRP) 通过eCIRP/TLR4通路调解冷压引起的AD恶化.
- 抑制eCIRP是一种有前途的治疗策略,可以应对感冒引起的血管紧急情况.
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