LL37/自我DNA复合体介导单细胞重编程
Aman Damara1, Joanna Wegner1, Emily R Trzeciak1
1Department of Dermatology, University Medical Center of the Johannes Gutenberg-University of Mainz, Mainz, Germany.
抗微生物LL37和自我DNA触发单细胞的炎症和表观遗传变化,导致像牛皮这样的自身免疫性疾病. 抑制KDM6A/B逆转了这些训练免疫效应,提供了治疗潜力.
科学领域:
- 免疫学 免疫学 免疫学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 代谢变化 代谢变化
背景情况:
- LL37和自我DNA复合体与牛皮和狼等自身免疫性疾病有关.
- 这些复杂物可以诱导髓状细胞的持久变化,影响免疫反应.
研究的目的:
- 研究LL37/自我DNA复合体对单细胞的长期代谢和表观遗传影响.
- 探索KDM6A/B在LL37/自我DNA诱导的训练免疫表型中的作用.
主要方法:
- 用LL37/自DNA复合体对单细胞的处理.
- 分析代谢活性 (糖解,氧化酸化) 和细胞因子的释放.
- 评估KDM6A/B表达和功能抑制.
- 对原始CD4+T细胞的影响的评估.
主要成果:
- LL37/自我DNA复合物诱导单细胞中的高代谢率和促炎性细胞因子释放,模仿牛皮单细胞.
- 在接受治疗的单细胞和牛皮患者的单细胞中,KDM6A/B脱甲基酶的调节升高.
- 抑制KDM6A/B可以逆转受过训练的免疫表型,减少炎症和T细胞诱导.
结论:
- LL37/自我DNA诱导的先天免疫记忆有助于牛皮病原.
- KDM6A/B在调解单细胞中训练免疫反应方面发挥着至关重要的作用.
- 针对KDM6A/B可能为牛皮和相关的自身免疫性疾病提供治疗策略.
更多相关视频
11:48Isolation Protocol of Mouse Monocyte-derived Dendritic Cells and Their Subsequent In Vitro Activation with Tumor Immune Complexes
Published on: May 31, 2018
08:31Characterization of Human Monocyte-derived Dendritic Cells by Imaging Flow Cytometry: A Comparison between Two Monocyte Isolation Protocols
Published on: October 18, 2016
相关概念视频
Methods of Nuclear Reprogramming
Somatic to iPS Cell Reprogramming
Lineage Commitment
Chromatin Modification in iPS Cells
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
Introduction to Nuclear Reprogramming
Differentiation of Common Myeloid Progenitor Cells
