PLX182335

GSE111650: The effects of Lef-1 overexpression on culture-expanded MECs

• Organsim mouse
• Type RNASEQ
• Target gene
• Project ARCHS4

The mouse trachea is thought to contain two distinct stem cell compartments that contribute to airway repairbasal cells in the surface airway epithelium (SAE) and an unknown submucosal gland (SMG) cell type. Whether a lineage relationship exists between these two stem cell compartments remains unclear. Usinglineage tracing of glandular myoepithelial cells (MECs), we demonstrate that MECs can give rise to seven cell types of the SAE and SMGs following severe airway injury. MECsprogressively adopted a basal cell phenotype on the SAE and established lasting progenitors capable of further regeneration following reinjury. MECs activate Wnt-regulated transcription factors (Lef-1/TCF7) following injury and Lef-1 induction in cultured MECs promoted transition to a basal cell phenotype. Surprisingly, dose-dependent MEC conditional activation of Lef-1 in vivo promoted self-limited airway regeneration in the absence of injury. Thus, modulating the Lef-1 transcriptional program in MEC-derived progenitors may have regenerative medicine applications for lung diseases. SOURCE: John,F,Engelhardt (john-engelhardt@uiowa.edu) - University of Iowa