[HTML][HTML] Integrin α6β4 identifies an adult distal lung epithelial population with regenerative potential in mice

HA Chapman, X Li, JP Alexander… - The Journal of …, 2011 - Am Soc Clin Investig
HA Chapman, X Li, JP Alexander, A Brumwell, W Lorizio, K Tan, A Sonnenberg, Y Wei…
The Journal of clinical investigation, 2011Am Soc Clin Investig
Laminins and their integrin receptors are implicated in epithelial cell differentiation and
progenitor cell maintenance. We report here that a previously unrecognized subpopulation
of mouse alveolar epithelial cells (AECs) expressing the laminin receptor α6β4, but little or
no pro–surfactant C (pro-SPC), is endowed with regenerative potential. Ex vivo, this
subpopulation expanded clonally as progenitors but also differentiated toward mature cell
types. Integrin β4 itself was not required for AEC proliferation or differentiation. An in vivo …
Laminins and their integrin receptors are implicated in epithelial cell differentiation and progenitor cell maintenance. We report here that a previously unrecognized subpopulation of mouse alveolar epithelial cells (AECs) expressing the laminin receptor α6β4, but little or no pro–surfactant C (pro-SPC), is endowed with regenerative potential. Ex vivo, this subpopulation expanded clonally as progenitors but also differentiated toward mature cell types. Integrin β4 itself was not required for AEC proliferation or differentiation. An in vivo embryonic lung organoid assay, which we believe to be novel, was used to show that purified β4+ adult AECs admixed with E14.5 lung single-cell suspensions and implanted under kidney capsules self-organized into distinct Clara cell 10-kDa secretory protein (CC10+) airway-like and SPC+ saccular structures within 6 days. Using a bleomycin model of lung injury and an SPC-driven inducible cre to fate-map AECs, we found the majority of type II AECs in fibrotic areas were not derived from preexisting type II AECs, demonstrating that SPC progenitor cells replenished type II AECs during repair. Our findings support the idea that there is a stable AEC progenitor population in the adult lung, provide in vivo evidence of AEC progenitor cell differentiation after parenchymal injury, and identify a strong candidate progenitor cell for maintenance of type II AECs during lung repair.
The Journal of Clinical Investigation