含氨酸的自组装β片对巨细胞极化和炎症反应的影响
Jacek K Wychowaniec1, Ezgi Irem Bektas1, Marcia Muerner1,2
1AO Research Institute Davos, Clavadelerstrasse 8, Davos 7270, Switzerland.
ACS applied materials & interfaces
|April 16, 2025
概括
自组合 (SAP) 调节免疫反应. 像EF8这样的特定序列促进了抗炎M2巨的两极分化,而YEF8诱导了亲炎M1巨,为免疫调节纳米生物材料提供了潜力.
科学领域:
- 生物材料科学 生物材料科学
- 纳米技术纳米技术
- 免疫学 免疫学 免疫学
背景情况:
- 自组装 (SAP) 是具有可调节结构的多功能纳米生物材料.
- 控制SAPs的纳米结构和化学特性是操纵细胞信号的关键.
- 了解SAP对先天免疫系统炎症信号的影响至关重要.
研究的目的:
- 设计和合成五个具有不同氨酸位置的β-sheet SAP.
- 研究这些SAP的化学和形态特征如何影响炎症信号.
- 探索SAPs作为免疫调节剂的潜力.
主要方法:
- 合成了五种β-sheet SAPs:EF8,YEF8,EF8Y,YEF8Y和EYF8,它们的定位不同.
- 描述了SAP自组装成纳米纤维及其捆绑性质.
- 使用THP-1细胞和初级人类PBMCs评估了炎症反应和巨分化 (M1/M2).
主要成果:
- 所有设计的SAP都形成了纳米纤维;YEF8和EF8显示捆绑.
- 可溶性EF8纳米纤维诱导了抗炎M2极化.
- 可溶性YEF8纳米纤维诱导了亲炎性M1极化.
- EF8Y,YEF8Y和EYF8没有引起显著的炎症反应.
- 结果在THP-1细胞和人类PBMC以及水凝培养物中一致.
结论:
- 序列,特别是氨酸的位置,决定了SAP的自我组装和免疫调节活性.
- EF8 和 YEF8 SAP 可以分别用作抗炎 (M2) 或促炎 (M1) 剂.
- 这些发现支持SAPs作为可调节的免疫调节纳米生物材料的开发,用于炎症疾病的治疗应用.
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