The unfolded protein response gene Ire1α is required for tissue renewal and normal differentiation in the mouse tongue and esophagus

The IRE1 alpha-XBP1s signaling branch of the unfolded protein response is a well-characterized survival pathway that allows cells to adapt to and resolve endoplasmic reticulum stress. Recent data has broadened our understanding of IRE1 alpha-XBP1s signaling beyond a stress response and revealed a physiological mechanism required for the dif-ferentiation and maturation of a wide variety of cell types. Here we provide evidence that the IRE1 alpha-XBP1s signaling pathway is required for the proliferation and maturation of basal keratinocytes in the mouse tongue and esophageal epithelium. Mice with conditional targeted deletion of either Ire1 alpha or Xbp1 in keratin 14 expressing basal keratinocytes displayed severe thinning of the lingual and esophageal mucosa that rendered them unable to eat. In IRE1 alpha null epithelium harvested at an earlier timepoint, genes regulating cell proliferation, cell-cell adhesion, and keratinization were significantly downregulated; indirect immunofluorescence revealed fewer proliferating basal keratinocytes, downregulation of E-cadherin, and thinning of the loricrin-positive granular and cornified layers. The number of Tp63-positive basal keratinocytes was reduced in the absence of IRE1 alpha, and expression of the Wnt pathway transcription factor LEF1, which is required for the proliferation of lingual transit amplifying cells, was also significantly downregulated at the transcript and protein level. Together these results reveal an essential role for IRE1 alpha-XBP1s in the maintenance of the stratified squamous epithelial tissue of the tongue and esophagus.

Automated summary

The IRE1 alpha-XBP1s signaling pathway is crucial for the proliferation and maturation of basal keratinocytes in the mouse tongue and esophageal epithelium, with its absence resulting in mucosal thinning and feeding impairment.