Tissue-specific transcriptional imprinting and heterogeneity in human innate lymphoid cells revealed by full-length single-cell RNA-sequencing

The impact of the microenvironment on innate lymphoid cell (ILC)-mediated immunity in humans remains largely unknown. Here we used full-length Smart-seq2 single-cell RNA-sequencing to unravel tissue-specific transcriptional profiles and heterogeneity of CD127(+) ILCs across four human tissues. Correlation analysis identified gene modules characterizing the migratory properties of tonsil and blood ILCs, and signatures of tissue-residency, activation and modified metabolism in colon and lung ILCs. Trajectory analysis revealed potential differentiation pathways from circulating and tissue-resident naive ILCs to a spectrum of mature ILC subsets. In the lung we identified both CRTH2(+) and CRTH2(-) ILC2 with lung-specific signatures, which could be recapitulated by alarmin-exposure of circulating ILC2. Finally, we describe unique TCR-V(D)J-rearrangement patterns of blood ILC1-like cells, revealing a subset of potentially immature ILCs with TCR-delta rearrangement. Our study provides a useful resource for in-depth understanding of ILC-mediated immunity in humans, with implications for disease.

Automated summary

This study utilized single-cell RNA sequencing to uncover tissue-specific transcriptional profiles and heterogeneity of CD127(+) ILCs in four human tissues. It identified migratory properties, tissue-residency, activation, and modified metabolism characteristics of ILCs in different tissues. The study also revealed potential differentiation pathways from naive to mature ILC subsets, and unique TCR-V(D)J-rearrangement patterns of blood ILC1-like cells.