Multi-transcription factor reporter mice delineate early precursors to the ILC and LTi lineages

Transcription factor (TF) reporter mice have proved integral to the characterization of murine innate lymphoid cell (ILC) development and function. Here, we implemented a CRISPR/Cas9-generated combinatorial reporter approach for the simultaneous resolution of several key TFs throughout ILC development in both the fetal liver and adult bone marrow. We demonstrate that the Tcf7-expressing early innate lymphoid precursor (EILP) and the common helper ILC precursor (CHILP) both contain a heterogeneous mixture of specified ILC and lymphoid tissue inducer (LTi) precursors with restricted lineage potential rather than a shared precursor. Moreover, the earliest specified precursor to the LTi lineage was identified upstream of these populations, before Tcf7 expression. These findings match dynamic changes in chromatin accessibility associated with the expression of key TFs (i.e., GATA3 and ROR gamma(t)), highlighting the distinct origins of ILC and LTi lineages at the epigenetic and functional levels, and provide a revised map for ILC development.

Automated summary

Utilizing a CRISPR/Cas9-generated combinatorial reporter approach, researchers demonstrated that the Tcf7-expressing early innate lymphoid precursor (EILP) and common helper ILC precursor (CHILP) contain a heterogeneous mixture of specified ILC and LTi precursors, rather than a shared precursor. The study also identified the earliest specified precursor to the LTi lineage, before Tcf7 expression, indicating distinct origins of ILC and LTi lineages at the epigenetic level. These findings provide a revised map for ILC development, highlighting the dynamic changes in chromatin accessibility associated with the expression of key TFs.