mTOR signaling is essential for epidermal development, yet the downstream mechanisms mediating its effects remain unclear. The 4E-BP1 (eukaryotic initiation factor 4E-binding protein 1), a major mTORC1 target that inhibits cap-dependent translation, has an undefined role in epidermal morphogenesis. In this study, we investigated the impact of 4E-BP1 loss on mTORC1 inactivation-mediated skin barrier defects. Eif4ebp1 -/- mice were generated using CRISPR/Cas9-mediated genome editing and crossed with epidermal-specific Rptor knockout (Rap EKO ) mice to obtain double-knockout (dKO) animals. Both Rap EKO and dKO neonates displayed fragile, shiny skin; rapid weight loss; and neonatal lethality. Toluidine blue assays revealed a partial restoration of barrier function in dKO mice. Histological analysis showed severe epidermal hypoplasia and loss of stratification in both mutants, whereas dKO mice exhibited mild and irregular cornification with slightly increased epidermal thickness. Proliferation remained impaired, but differentiation markers were partially restored in dKO epidermis. These findings demonstrate that 4E-BP1 deletion modestly alleviates the differentiation and barrier defects caused by mTORC1 inactivation but does not prevent neonatal lethality, suggesting that 4E-BP1 is not the major downstream effector of mTORC1 during epidermal morphogenesis.
Tang et al. (Wed,) studied this question.