反应性氧物种-响应性纳米粒子 输送小干扰性核糖酸向动脉样硬化嗅觉受体2的治疗 治疗神经硬化
Huaner Ni1,2, Hui Zhou1, Xin Liang1
1State Key Laboratory of Organic Electronics and Information Displays & Institute of Advanced Materials (IAM), Nanjing University of Posts & Telecommunications, Nanjing 210023, China.
ACS nano
|August 14, 2024
概括
这项研究介绍了一种用于动脉样硬化 (AS) 的新型神经解剖纳米平台. 它使用小干扰性核糖核酸 (siRNA) 向巨细胞中的嗅觉受体2 (Olfr2),有效治疗AS,并通过光声成像进行诊断.
科学领域:
- 心血管研究研究心血管研究
- 纳米医学是一种纳米医学.
- 分子生物学分子生物学
背景情况:
- 动脉样硬化 (AS) 是一种由动脉脂质斑块标志着的慢性炎症性疾病.
- 小干扰核糖核酸 (siRNA) 疗法为AS提供精确的基因抑制,但面临着有限的巨细胞标.
- 嗅觉受体2 (Olfr2) 是AS斑块形成的新发现的潜在目标.
研究的目的:
- 开发和评估一个用于针对性地将抗Olfr2 siRNA (si-Olfr2) 输送到动脉样硬化病变中的巨细胞的光纳米平台.
- 为了降低Olfr2表达,用于AS治疗,并使用光声成像 (PAI) 进行诊断.
主要方法:
- 针对巨细胞的抗Olfr2 siRNA (si-Olfr2) 的设计.
- 开发一种响应活性氧物种 (ROS) 的纳米载体系统,用于封装si-Olfr2.
- 在第二个近红外 (NIR-II) 窗口中使用光声成像 (PAI) 进行诊断.
主要成果:
- 在动脉样硬化斑块内的巨细胞中有效下调Olfr2表达.
- 抑制含有3 (NLRP3) 炎症酶激活和互白素-1β (IL-1β) 分泌的NLR家族皮林域.
- 减少动脉样硬化斑块的形成,脂质沉积,巨细胞的亡和死角区域,以及减轻炎症.
结论:
- 这项研究展示了一种用于针对性地将si-Olfr2输送到损伤性巨细胞的theranostic纳米平台的概念证明.
- 这个平台显示出对动脉样硬化的诊断和治疗都有潜力.
- 这些发现强调了Olfr2作为AS的可行的治疗点.
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