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Relb acts downstream of medullary thymic epithelial stem cells and is essential for the emergence of RANK+ medullary epithelial progenitors

机译:Relb在胸腺髓样上皮干细胞的下游起作用对于RANK +髓样上皮祖细胞的出现至关重要

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摘要

Thymic epithelial cells (TECs) provide essential signals for αβT‐cell development, and medullary TECs (mTECs) control T‐cell tolerance through both negative selection and Foxp3+ regulatory T (Treg) cell development. Although heterogeneity within the mTEC compartment is well studied, the molecular regulators of specific stages of mTEC development are still poorly understood. Given the importance of the RANK‐RANKL axis in thymus medulla formation, we have used RANK Venus reporter mice to analyze the ontogeny of RANK+ TECs during development and correlated RANK expression with mTEC stem cells defined by SSEA‐1. In addition, we have investigated how requirements for the key regulators Foxn1 and Relb map to specific stages of mTEC development. Here, we show SSEA‐1+ mTEC stem cells emerge prior to RANK expression and are present in both nude and Relb −/− mice, providing direct evidence that mTEC lineage specification occurs independently of Foxn1 and Relb. In contrast, we show that Relb is necessary for the effective production of downstream RANK+ mTEC progenitors. Collectively, our work defines stage‐specific requirements for critical TEC regulators during medulla development, including the timing of Relb dependency, and provides new information on mechanisms controlling mTEC specification.
机译:胸腺上皮细胞(TECs)为αβT细胞发育提供了重要信号,而髓质TEC(mTECs)通过阴性选择和Foxp3 + 调节性T(Treg)细胞发育来控制T细胞耐受性。尽管对mTEC隔室内的异质性进行了很好的研究,但对mTEC发展的特定阶段的分子调节剂仍然知之甚少。考虑到RANK‐RANKL轴在胸腺髓质形成中的重要性,我们已使用RANK Venus报告基因小鼠分析了发育过程中RANK + TEC的个体发育,并将RANK表达与SSEA-定义的mTEC干细胞相关联。 1。此外,我们研究了关键调节器Foxn1和Relb的要求如何映射到mTEC开发的特定阶段。在这里,我们显示了SSEA-1 + mTEC干细胞在RANK表达之前出现,并且存在于裸鼠和Relb -/-小鼠中,提供了mTEC谱系规格的直接证据。发生独立于Foxn1和Relb。相反,我们表明Relb是有效生产下游RANK + mTEC祖细胞所必需的。我们的工作共同定义了延髓开发过程中关键TEC调节器的特定阶段要求,包括Relb依赖的时间,并提供了有关控制mTEC规范的机制的新信息。

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