In post-mitotic neurons, several tumor suppressor genes (TSGs) including p53, Rb and PTEN modulate the axon regeneration success after injury. Particularly, PTEN inhibition is a key driver of successful CNS axon regeneration after optic nerve or spinal cord injury. In contrast, in peripheral neurons, TSG influence in neuronal morphology, physiology and pathology has not been investigated to the same depth. In this study we conditionally deleted PTEN from mouse facial motoneurons ( Ptenflox/flox; Chat-Cre ) and analyzed neuronal responses in vivo with or without peripheral facial nerve injury in male and female mice. In uninjured motoneurons, PTEN loss induced somatic, axonal and nerve hypertrophy, synaptic terminal enlargement and reduction in physiological whisker movement. Despite these morphological and physiological changes, PTEN deletion positively regulated facial nerve regeneration and recovery of whisker movement after nerve injury. Regenerating PTEN deficient motoneurons upregulated P-CREB and a s...