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Abstract
Phosphatidylethanolamine undergoes dynamic metabolic reprogramming during liver regeneration, with phospholipid phosphatase 2 (PLPP2) showing significant changes.
- The specific metabolic shift that initiates liver cell regeneration remains unclear, despite the liver's known regenerative capacity.
- Alterations in PLPP2 were observed in liver biopsy samples from patients with drug-induced liver injury.
- In mouse models, the deletion of PLPP2 in liver cells worsened acute liver injury.
- During liver regeneration, the resolution of endoplasmic reticulum (ER) stress was linked to an increase in PLPP2 levels.
- Phosphatidylethanolamine supports liver repair by binding to PEBP1, enhancing its interaction with GLI1, which prevents the degradation of GLI1.
- PE also promotes autophagy by aiding the lipidation of LC3B and helps alleviate ER stress through increased ER-localized PE.
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