Identification of fibroblast progenitors in the developing mouse thymus

The thymus stroma constitutes a fundamental microenvironment for T-cell generation. Despite the chief contribution of thymic epithelial cells, recent studies emphasize the regulatory role of mesenchymal cells in thymic function. Mesenchymal progenitors are suggested to exist in the postnatal thymus; nonetheless, an understanding of their nature and the mechanism controlling their homeostasis in vivo remains elusive. We resolved two new thymic fibroblast subsets with distinct developmental features. Whereas CD140 alpha beta(+)GP38(+)SCA-1(-) cells prevailed in the embryonic thymus and declined thereafter, CD140 alpha beta(+)GP38(+)SCA-1(+) cells emerged in the late embryonic period and predominated in postnatal life. The fibroblastic-associated transcriptional programme was upregulated in CD140 alpha beta(+)GP38(+)SCA-1(+) cells, suggesting that they represent a mature subset. Lineage analysis showed that CD140 alpha beta(+)GP38(+)SCA1(+) maintained their phenotype in thymic organoids. Strikingly, CD140 alpha beta(+)GP38(+)SCA-1(-) generated CD140 alpha beta(+)GP38(+)SCA-1(+), inferring that this subset harboured progenitor cell activity. Moreover, the abundance of CD140 alpha beta(+)GP38(+)SCA-1(+) fibroblasts was gradually reduced in Rag2(-/-) and Rag2(-/-)Il2rg(-/-) thymi, indicating that fibroblast maturation depends on thymic crosstalk. Our findings identify CD140 alpha beta(+)GP38(+)SCA-1(-) as a source of fibroblast progenitors and define SCA-1 as a marker for developmental stages of thymic fibroblast differentiation.

Automated summary

This study identified two distinct subsets of thymic fibroblasts, CD140 alpha beta(+)GP38(+)SCA-1(-) and CD140 alpha beta(+)GP38(+)SCA-1(+), with different developmental features. CD140 alpha beta(+)GP38(+)SCA-1(-) was identified as a source of fibroblast progenitors, while CD140 alpha beta(+)GP38(+)SCA-1(+) represented a mature subset. Furthermore, the study found that thymic crosstalk is crucial for fibroblast maturation.