Department of Hematology, Oncology, Immunology, and Rheumatology, University Hospital of Tübingen, Tübingen, Germany.
Centre for Organismal Studies (COS), Heidelberg University, Heidelberg, Germany.
Eur J Immunol. 2022 Feb;52(2):261-269. doi: 10.1002/eji.202149512. Epub 2021 Nov 17.
The differentiation of T cells from lymphoid progenitors in the thymus follows sequential developmental stages that constantly require interaction with thymic epithelial cells. Several distinct aspects of early T cell development depend on the activation of Notch receptors on thymocytes, while the selection of thymocytes at later stages are believed to be Notch independent. Using reverse genetic approaches and whole-thymus live imaging in an in vivo teleost model, the medaka, we report that Notch1 signals is required for proliferation and specification of developing T cells as well as involved in their selection in the thymus. We reveal that Notch1 controls the migratory behavior of thymocytes through controlling the chemokine receptor Ccr9b and thereby influence the T cell receptor (TCR) activation. Hence, we propose that, in lower vertebrates, the function of Notch signaling extends to all stages of T cell development, except when thymocytes undergo TCRβ rearrangement.
T 细胞从胸腺中的淋巴祖细胞分化遵循连续的发育阶段,这些阶段不断需要与胸腺上皮细胞相互作用。早期 T 细胞发育的几个不同方面依赖于胸腺细胞上 Notch 受体的激活,而后期阶段的胸腺细胞选择被认为是 Notch 非依赖性的。我们使用反向遗传方法和活体成像技术,在一种活体硬骨鱼模型——斑马鱼中,报告了 Notch1 信号在发育中的 T 细胞的增殖和特化以及在胸腺中的选择中是必需的。我们揭示了 Notch1 通过控制趋化因子受体 Ccr9b 来控制胸腺细胞的迁移行为,从而影响 T 细胞受体 (TCR) 的激活。因此,我们提出,在低等脊椎动物中,Notch 信号的功能扩展到 T 细胞发育的所有阶段,除了胸腺细胞经历 TCRβ 重排时。