循环蛋白与亡过程和糖尿病中末期病的快速发展有关
Katsuhito Ihara1,2,3, Eiichiro Satake1,2, Parker C Wilson4,5
1Research Division, Joslin Diabetes Center, Boston, Massachusetts, USA.
JCI insight
|October 22, 2024
概括
高水平的特定循环蛋白质,特别是那些参与细胞亡和TNF受体信号传递的蛋白质,可以预测糖尿病患者患末期病 (ESKD) 的风险.
科学领域:
- 蛋白质组学是指蛋白质组学.
- 腎臟病學 (nephrology) 是一種醫學.
- 分子生物学分子生物学
背景情况:
- 与末期病 (ESKD) 风险相关的循环蛋白质缺乏明确的起源和生物途径关联.
- 了解这些蛋白质来源对于识别糖尿病病中的疾病机制至关重要.
研究的目的:
- 在糖尿病患者中识别与ESKD风险相关的循环蛋白质.
- 研究这些蛋白质的生物通路和细胞起源.
- 使用蛋白质生物标志物开发ESKD风险的预测模型.
主要方法:
- 奥林克蛋白质组学平台用于测量399名糖尿病患者的455种血蛋白.
- 纵向跟踪 (7-15年) 来追踪ESKD的发展 (n=143).
- 在外围白细胞 (WBC) 和脏活检的单核RNA-Seq中进行基因表达分析.
主要成果:
- 46种与ESKD风险相关的循环蛋白 (P < 1 × 10-5).
- 20种蛋白质丰富了亡/TNF受体信号通路;亡得分预测了ESKD风险.
- 这些蛋白质的基因在受伤的脏靠近管细胞中表达过多,而不是白细胞.
结论:
- 循环蛋白质的升高,特别是那些表明细胞亡和TNF受体信号的蛋白质,可能来自受伤的细胞.
- 这些蛋白质生物标志物,特别是亡评分,可以预测糖尿病患者的ESKD发展.
- 研究结果强调,脏是ESKD风险循环生物标志物的来源.
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