HMGB2 Promotes De Novo Lipogenesis to Accelerate Hepatocyte Proliferation During Liver Regeneration.
Narantsog ChoijookhuuKoichi YanoBaljinnyam Lkham-ErdeneShinichiro ShirouzuToshiki Kubotanull FidyaTakumi IshizukaKengo KaiEtsuo ChosaYoshitaka HishikawaPublished in: The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society (2024)
Liver regeneration is a well-orchestrated compensatory process that is regulated by multiple factors. We recently reported the importance of the chromatin protein, a high-mobility group box 2 (HMGB2) in mouse liver regeneration. However, the molecular mechanism remains unclear. In this study, we aimed to study how HMGB2 regulates hepatocyte proliferation during liver regeneration. Seventy-percent partial hepatectomy (PHx) was performed in wild-type (WT) and HMGB2-knockout (KO) mice, and the liver tissues were used for microarray, immunohistochemistry, quantitative polymerase chain reaction (qPCR), and Western blotting analyses. In the WT mice, HMGB2-positive hepatocytes colocalized with cell proliferation markers. In the HMGB2-KO mice, hepatocyte proliferation was significantly decreased. Oil Red O staining revealed the transient accumulation of lipid droplets at 12-24 hr after PHx in the WT mouse livers. In contrast, decreased amount of lipid droplets were found in HMGB2-KO mouse livers, and it was preserved until 36 hr. The microarray, immunohistochemistry, and qPCR results demonstrated that the expression of lipid metabolism-related genes was significantly decreased in the HMGB2-KO mouse livers. The in vitro experiments demonstrated that a decrease in the amount of lipid droplets correlated with decreased cell proliferation activity in HMGB2-knockdown cells. HMGB2 promotes de novo lipogenesis to accelerate hepatocyte proliferation during liver regeneration.
Keyphrases
- stem cells
- cell proliferation
- wild type
- high fat diet induced
- gene expression
- fatty acid
- liver injury
- magnetic resonance
- genome wide
- magnetic resonance imaging
- computed tomography
- type diabetes
- binding protein
- transcription factor
- small molecule
- dna methylation
- metabolic syndrome
- cell death
- brain injury
- blood brain barrier
- endoplasmic reticulum stress
- pi k akt