# PGC-1α protects against MASH via Tim23-dependent inhibition of DRP1-mediated ferroptosis

## TL;DR

This study shows that PGC-1α protects the liver from MASH by preventing a type of cell death called ferroptosis through a specific molecular pathway.

## Contribution

The study reveals a novel mechanism by which PGC-1α inhibits hepatocyte ferroptosis via Tim23 and DRP1 in MASH.

## Key findings

- PGC-1α deficiency worsens hepatocyte ferroptosis in MASH models.
- PGC-1α overexpression reduces ferroptosis and MASH severity.
- PGC-1α inhibits ferroptosis by promoting Tim23 and blocking the Drp1-ACSL4 pathway.

## Abstract

Peroxisome proliferator-activated receptor gamma coactivator 1α (PGC-1α) is crucial for mitochondrial function and biogenesis. However, whether and how PGC-1α can regulate hepatocyte ferroptosis during the pathogenic process of metabolic dysfunction-associated steatohepatitis (MASH) has not been clarified. Hepatocyte ferroptosis was assessed in the liver of MASH patients and in vivo and in vitro MASH models. The mechanisms by which PGC-1α regulated hepatocyte ferroptosis during the process of MASH were examined by Western blot, reverse transcription quantitative polymerase chain reaction (RT-qPCR), immunofluorescence, luciferase reporter, and co-immunoprecipitation assays. Hepatocyte ferroptosis, down-regulated Tim23 and up-regulated ACSL4 expression were observed in the livers of MASH patients, and in vivo and in vitro MASH models. PGC-1α deficiency exacerbated hepatocyte ferroptosis in mouse models of MASH induced by high-fat diet and methionine- and choline-deficient diet, and primary mouse hepatocytes that had been treated with palmitic acid. Conversely, PGC-1α over-expression mitigated hepatocyte ferroptosis in these models. Mechanistically, PGC-1α promoted the binding of nuclear respiratory factor (Nrf)1 to the Tim23 promoter, reducing Drp1 transcription and ACSL4 mitochondrial translocation, inhibiting hepatocyte ferroptosis and MASH. These findings indicated that PGC-1α inhibited hepatocyte ferroptosis and attenuated MASH by upregulating Tim23 and inhibiting the Drp1-ACSL4 axis.