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在患有深静脉血栓症的小鼠中,IL-10和TGF-β1的时间依赖的顺序变化
Juan-Juan Wu1,2,3, Jun-Jie Huang1,2,3, Yu Zhang1,2,3
1Department of Forensic Medicine, Wenzhou Medical University, Wenzhou 325035, Zhejiang Province, China.
Fa yi xue za zhi
|June 7, 2024
概括
在深静脉血栓症 (DVT) 小鼠模型中,因特乐金-10 (IL-10) 和转化生长因子-β1 (TGF-β1) 的表达随着时间的推移而发生变化. 这些细胞因子水平可以帮助估计血栓年龄.
科学领域:
- 生物医学科学 生物医学科学
- 免疫学 免疫学 免疫学
- 血栓形成研究研究
背景情况:
- 深静脉血栓症 (DVT) 是一种重要的临床疾病.
- 准确估计血栓年龄对于有效治疗至关重要.
- 特定细胞因子在DVT演变中的作用需要进一步研究.
研究的目的:
- 在小鼠模型中研究在DVT发育期间IL-10和TGF-β1的时间表达模式.
- 评估IL-10和TGF-β1作为估计血栓年龄的生物标志物的潜力.
主要方法:
- 通过下静脉绑建立了一个DVT小鼠模型.
- 血栓样本在不同的时间点收集 (1-21天结后).
- 免疫组织化学 (IHC),西式涂抹和qPCR用于量化IL-10和TGF-β1的表达.
主要成果:
- 主要检测到IL-10和TGF-β1是在瘤内的单细胞和纤维细胞样细胞中.
- 与对照组相比,IL-10和TGF-β1在DVT样本中的表达显著增加.
- 对IL-10mRNA和蛋白质的峰值表达水平分别在7天和10天观察到.
- 对TGF-β1mRNA和蛋白质的峰值表达水平分别在第10天和第14天观察到.
结论:
- 在DVT进展过程中,IL-10和TGF-β1的表达呈现出时间依赖的变化.
- 这些细胞因子表达特征为估计深静脉血栓瘤的年龄提供了潜在的基础.
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