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Isolation of Murine Lymph Node Stromal Cells
Published on: August 19, 2014
删除耐受度由外心空气表达细胞介导
James M Gardner1, Jason J Devoss, Rachel S Friedman
1Diabetes Center, University of California San Francisco (UCSF), San Francisco, CA 94122, USA.
在淋巴体器官中发现了外皮表达细胞 (eTACs),揭示了预防自身免疫的新机制. 这些细胞消除了脱离胆髓的自我反应性T细胞,增强了免疫耐受性.
科学领域:
- 免疫学 免疫学 免疫学
- 自免疫性研究的研究.
- T细胞生物学T细胞生物学
背景情况:
- 自免疫源于自我反应性T细胞,需要在发育过程中消除它们.
- 胸腺,通过自身免疫调节 (Aire) 基因,表达自我抗原来消除这些T细胞.
- 有一个潜在的差距存在于T细胞逃脱胸膜选择.
研究的目的:
- 确定参与预防自身免疫的新型细胞机制.
- 为了研究外皮细胞在T细胞耐受性中的作用.
- 了解免疫耐受性如何保持在甲状腺之外.
主要方法:
- 鉴定和表征异体气体表达细胞 (eTACs).
- 通过eTACs对自我抗原表达的分析.
- 在体内使用双光子显微镜观察T细胞-eTAC相互作用.
- 评估eTACs消除自身反应性T细胞的能力.
主要成果:
- 在二次淋巴体器官中鉴定出了空气表达细胞 (eTAC).
- eTACs表达出各种各样的自我抗原.
- 观察到eTACs和自身反应性T细胞之间的稳定,抗原特异性相互作用.
- eTACs证明了删除自身反应性T细胞的能力.
结论:
- 一个二级网络的额外体细胞有助于免疫耐受性.
- eTACs在消除逃避胸膜负性选择的自反应性T细胞方面发挥着至关重要的作用.
- 这种额外免疫机制增强了自我耐受性,并防止了自身免疫.
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