A high resolution map of a lung regeneration time course in the context of aging.

Link to interactive webtool: Lung Injury and Regeneration in Old and Young Mice

Link to the preprint: Single cell decomposition of multicellular aging programs associated with impaired lung regeneration | bioRxiv

Aging impairs the regenerative capacity of mammalian organs and is a major risk factor for chronic lung disease. The causalities for persistent fibrosis after lung injury in old individuals have been unclear. We used longitudinal single-cell RNA-seq after lung injury and dissected aging effects computationally and experimentally at baseline and during repair. In old mice, sustained fibroblast activation in the resolution phase of repair was associated with prolonged cellular senescence and persistent epithelial-mesenchymal crosstalk. Single-cell interpretable tensor decomposition analysis identified the strongest link of aging with T/B-lymphocytes and macrophages. A Gzmk-high CD8-T cell state was unique to aged mice, co-localized with progenitors, and its co-culture or Gzmk treatments in lung organoids reduced progenitor function by induction of stem cell senescence. In summary, our study highlights effects of immune aging on progenitor function and provides a high resolution map of a lung regeneration time course in the context of aging.