Autophagy Sustains the Proliferative Capacity of AT2 Cells during BLM Injury
(A) CFEs of mouse AT2 cells isolated from untreated or BLM-injured Atg5f/f mice at day 10 after seeding (n = 4).
(B) Representative micrographs of organoid cultures of mouse AT2 cells isolated from Atg5f/f, SftpcCreER;Atg5f/f (pretreated with tamoxifen), or Nkx2.1Cre;Atg5f/f mice 14 days after BLM injury. Scale bar: 200 μm.
(C and D) CFEs (C) and sizes (D) of organoid colonies from Atg5f/f, SftpcCreER;Atg5f/f (pretreated with tamoxifen), or Nkx2.1Cre;Atg5f/f mice at day 14 after BLM injury (n = 4).
(E and F) (E) Immunostaining of organoid colonies and (F) quantification of fractions of Ki67+pro-SPC+ cells in total pro-SPC+ cells in AT2 organoids (n = 4). Data are representative of three independent experiments with error bars representing the mean ± SD. ∗p < 0.05.