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Author:
Date:
2016-03-20
[Abstract] Subtypes of innate lymphoid cells (ILC), defined based on their cytokine secretion profiles and transcription factor expression, are important for host protection from pathogens and maintaining tissue homeostasis. ILCs develop from common lymphoid progenitors (CLP) in the bone marrow. Using the methods described here, we have previously shown that loss of the transcriptional regulator TOX (Thymocyte-selection associated HMG-box protein) leads to specific changes in ILC development and differentiation. Here, we describe how to obtain ILCs from in vivo isolated CLP grown in vitro.
[摘要] 先天淋巴细胞（ILC）的亚型，基于其细胞因子分泌谱和转录因子表达来定义，对于宿主保护免于病原体和维持组织内稳态是重要的。 ILC从骨髓中的普通淋巴祖细胞（CLP）发展而来。 使用本文所述的方法，我们以前显示转录调节器TOX（胸腺细胞选择相关的HMG框蛋白）的损失导致ILC发展和分化的具体变化。 在这里，我们描述了如何从体内分离的CLP获得ILC。
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