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Single-cell RNA-sequencing identifies the developmental trajectory of C-Myc-dependent NK1.1- T-bet+ intraepithelial lymphocyte precursors.


ABSTRACT: Natural intraepithelial lymphocytes (IELs) are thymus-derived adaptive immune cells, which are important contributors to intestinal immune homeostasis. Similar to other innate-like T cells, they are induced in the thymus through high-avidity interaction that would otherwise lead to clonal deletion in conventional CD4 and CD8 T cells. By applying single-cell RNA-sequencing (scRNA-seq) on a heterogeneous population of thymic CD4-CD8??-TCR??+NK1.1- IEL precursors (NK1.1- IELPs), we define a developmental trajectory that can be tracked based on the sequential expression of CD122 and T-bet. Moreover, we identify the Id proteins Id2 and Id3 as a novel regulator of IELP development and show that all NK1.1- IELPs progress through a PD-1 stage that precedes the induction of T-bet. The transition from PD-1 to T-bet is regulated by the transcription factor C-Myc, which has far reaching effects on cell cycle, energy metabolism, and the translational machinery during IELP development. In summary, our results provide a high-resolution molecular framework for thymic IEL development of NK1.1- IELPs and deepen our understanding of this still elusive cell type.

SUBMITTER: Hummel JF 

PROVIDER: S-EPMC7039806 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature

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Single-cell RNA-sequencing identifies the developmental trajectory of C-Myc-dependent NK1.1<sup>-</sup> T-bet<sup>+</sup> intraepithelial lymphocyte precursors.

Hummel Jonas F JF   Zeis Patrice P   Ebert Karolina K   Fixemer Jonas J   Konrad Philip P   Schachtrup Christian C   Arnold Sebastian J SJ   Grün Dominic D   Tanriver Yakup Y  

Mucosal immunology 20191111 2


Natural intraepithelial lymphocytes (IELs) are thymus-derived adaptive immune cells, which are important contributors to intestinal immune homeostasis. Similar to other innate-like T cells, they are induced in the thymus through high-avidity interaction that would otherwise lead to clonal deletion in conventional CD4 and CD8 T cells. By applying single-cell RNA-sequencing (scRNA-seq) on a heterogeneous population of thymic CD4<sup>-</sup>CD8αβ<sup>-</sup>TCRαβ<sup>+</sup>NK1.1<sup>-</sup> IEL pr  ...[more]

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