Nozais Mathis, Loosveld Marie, Pankaew Saran, Grosjean Clémence, Gentil Noémie, Quessada Julie, Nadel Bertrand, Mionnet Cyrille, Potier Delphine, Payet-Bornet Dominique
Aix Marseille Univ, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), Parc scientifique de Luminy, Case 906, 13288 Marseille cedex 9, France.
APHM, Hôpital La Timone, Laboratoire d'Hématologie, Marseille, France.
iScience. 2021 Jun 19;24(7):102761. doi: 10.1016/j.isci.2021.102761. eCollection 2021 Jul 23.
In the thymus, T cell progenitors differentiate in order to generate naive T lymphocytes which migrate in the periphery where they will fulfill their function in the adaptive immune response. During thymopoiesis, genomic alterations in thymocytes can promote leukemia development. Among recurrent alteration is inactivation, which is associated to MYC overexpression. Herein, we used conditional and knockout mouse models and single-cell RNA-sequencing approach, to investigate the impact of MYC loss on physio-pathological development of PTEN-proficient or PTEN-deficient T lymphocytes. First, our results confirm that MYC is mandatory for PTEN loss-mediated leukemogenesis, while it is not required for terminal steps of thymopoiesis. In contrast, we uncovered that ablation in CD4CD8 thymocytes disrupts T lymphocytes homeostasis in the spleen, notably by drastically reducing the number of MYC-deficient effector/memory T cells. Collectively, our data show that besides naive T cells proliferation, MYC is essential for effector/memory differentiation.
在胸腺中,T细胞祖细胞发生分化,以产生初始T淋巴细胞,这些细胞迁移至外周,在适应性免疫反应中发挥作用。在胸腺生成过程中,胸腺细胞的基因组改变可促进白血病的发展。常见的改变之一是失活,这与MYC的过表达有关。在此,我们使用条件性和基因敲除小鼠模型以及单细胞RNA测序方法,来研究MYC缺失对PTEN功能正常或PTEN缺陷的T淋巴细胞生理病理发育的影响。首先,我们的结果证实,MYC对于PTEN缺失介导的白血病发生是必需的,而胸腺生成的终末步骤则不需要它。相反,我们发现CD4CD8胸腺细胞中的基因敲除会破坏脾脏中T淋巴细胞的稳态,特别是通过大幅减少MYC缺陷的效应/记忆T细胞的数量。总体而言,我们的数据表明,除了初始T细胞增殖外,MYC对于效应/记忆分化也是必不可少的。