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经典的 Notch 信号通路控制了胎胸腺发育过程中早期胸腺上皮祖细胞状态和骨髓上皮谱系的出现。

Canonical Notch signaling controls the early thymic epithelial progenitor cell state and emergence of the medullary epithelial lineage in fetal thymus development.

机构信息

MRC Centre for Regenerative Medicine, Institute for Stem Cell Research, School of Biological Sciences, 5, Little France Drive, Edinburgh EH16 4UU, UK.

Biotech Research and Innovation Centre (BRIC), Ole Maaløes Vej 5, 2200 Copenhagen, Denmark.

出版信息

Development. 2020 Jun 22;147(12):dev178582. doi: 10.1242/dev.178582.

Abstract

Thymus function depends on the epithelial compartment of the thymic stroma. Cortical thymic epithelial cells (cTECs) regulate T cell lineage commitment and positive selection, while medullary (m) TECs impose central tolerance on the T cell repertoire. During thymus organogenesis, these functionally distinct sub-lineages are thought to arise from a common thymic epithelial progenitor cell (TEPC). However, the mechanisms controlling cTEC and mTEC production from the common TEPC are not understood. Here, we show that emergence of the earliest mTEC lineage-restricted progenitors requires active NOTCH signaling in progenitor TEC and that, once specified, further mTEC development is NOTCH independent. In addition, we demonstrate that persistent NOTCH activity favors maintenance of undifferentiated TEPCs at the expense of cTEC differentiation. Finally, we uncover a cross-regulatory relationship between NOTCH and FOXN1, a master regulator of TEC differentiation. These data establish NOTCH as a potent regulator of TEPC and mTEC fate during fetal thymus development, and are thus of high relevance to strategies aimed at generating/regenerating functional thymic tissue and .

摘要

胸腺功能依赖于胸腺基质的上皮细胞区室。皮质胸腺上皮细胞(cTEC)调节 T 细胞谱系的决定和阳性选择,而髓质(m)TEC 对 T 细胞库施加中枢耐受。在胸腺器官发生过程中,这些功能上不同的亚谱系被认为来自于共同的胸腺上皮祖细胞(TEPC)。然而,控制从共同的 TEPC 产生 cTEC 和 mTEC 的机制尚不清楚。在这里,我们表明,最早的 mTEC 谱系限制祖细胞的出现需要祖细胞 TEC 中活跃的 NOTCH 信号,并且一旦指定,进一步的 mTEC 发育是 NOTCH 独立的。此外,我们证明持续的 NOTCH 活性有利于未分化的 TEPC 的维持,而牺牲 cTEC 的分化。最后,我们揭示了 NOTCH 和 FOXN1 之间的交叉调节关系,FOXN1 是 TEC 分化的主要调节因子。这些数据确立了 NOTCH 作为胎儿胸腺发育过程中 TEPC 和 mTEC 命运的有效调节剂,因此与旨在生成/再生功能性胸腺组织的策略密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee1/7328009/81f212706e8e/develop-147-178582-g1.jpg

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