来自结性脊柱炎患者的血外体的蛋白质和基因组分析
Fataneh Tavasolian1, Starlee Lively1,2, Chiara Pastrello1,2,3
1Schroeder Arthritis Institute, Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada.
Annals of the rheumatic diseases
|August 2, 2023
概括
脊髓灰质炎 (AS) 患者表现出明显的外体样本,具有改变的microRNA (miRNA) 和蛋白质表达,有助于免疫失调. 来自AS的外体抑制了调节性T细胞的增殖,提供了对疾病病原和潜在治疗点的见解.
科学领域:
- 免疫学 免疫学 免疫学
- 基因组学就是基因组学.
- 蛋白质组学是指蛋白质组学.
- 异构体生物学 异构体生物学
背景情况:
- 脊髓灰质炎 (AS) 的发病包括免疫失调,由改变的基因,microRNA (miRNA) 和蛋白质表达的潜在贡献.
- 外基因组通过miRNA运输参与细胞间通信,涉及到延续AS的炎症.
研究的目的:
- 在AS患者中进行第一个血衍生外体的蛋白质和miRNA分析.
- 研究AS衍生的外体对CD4+T细胞,特别是调控性T细胞 (Tregs) 的功能影响.
主要方法:
- 从AS患者和健康对照组 (HC) 中分离和表征血衍生的外体,使用超离心和流细胞计.
- 对外体表面标记物和细胞因子概况的多重免疫捕获试验.
- 下一代测序用于miRNA识别和计算生物学分析.
- 与AS外生体和HC CD4+ T细胞进行共同培养实验,以评估T细胞子集的频率和增殖.
主要成果:
- 与HC患者相比,AS患者的外体标记CD63和CD81的表达增加.
- 在AS衍生的外体中降低IL-8和IL-10的调节;在与HC CD4+ T细胞共同培养时,IFNα2和IL-33的上调调节.
- 亚氏体外体抑制了FOXP3+调节性T细胞 (Tregs) 的增殖.
- 微RNA测序确定了AS外体中24个差异表达的微RNA,其中22个是上调的,2个是下调的.
结论:
- 患有AS的个体具有独特的基于外体的免疫学和遗传特征.
- 在AS中Treg增殖的外体介导抑制表明有助于该疾病中T细胞激活的机制.
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