APE1/Ref-1 Inhibits Adipogenic Transcription Factors during Adipocyte Differentiation in 3T3-L1 Cells.
Eun-Ok LeeHee-Kyoung JooYu-Ran LeeSung-Min KimKwon-Ho LeeSang-Do LeeByeong Hwa JeonPublished in: International journal of molecular sciences (2023)
Apurinic/apyrimidinic endonuclease 1/redox factor-1 ( APE1/Ref-1 ) is a multifunctional protein involved in DNA repair and redox regulation. The redox activity of APE1/Ref-1 is involved in inflammatory responses and regulation of DNA binding of transcription factors related to cell survival pathways. However, the effect of APE1/Ref-1 on adipogenic transcription factor regulation remains unknown. In this study, we investigated the effect of APE1/Ref-1 on the regulation of adipocyte differentiation in 3T3-L1 cells. During adipocyte differentiation, APE1/Ref-1 expression significantly decreased with the increased expression of adipogenic transcription factors such as CCAAT/enhancer binding protein ( C/EBP )- α and peroxisome proliferator-activated receptor ( PPAR )- γ , and the adipocyte differentiation marker adipocyte protein 2 ( aP2 ) in a time-dependent manner. However, APE1/Ref-1 overexpression inhibited C/EBP-α , PPAR-γ, and aP2 expression, which was upregulated during adipocyte differentiation. In contrast, silencing APE1/Ref-1 or redox inhibition of APE1/Ref-1 using E3330 increased the mRNA and protein levels of C/EBP-α , PPAR-γ , and aP2 during adipocyte differentiation. These results suggest that APE1/Ref-1 inhibits adipocyte differentiation by regulating adipogenic transcription factors, suggesting that APE1/Ref-1 is a potential therapeutic target for regulating adipocyte differentiation.
Keyphrases
- transcription factor
- insulin resistance
- binding protein
- dna binding
- adipose tissue
- fatty acid
- dna repair
- poor prognosis
- induced apoptosis
- type diabetes
- skeletal muscle
- dna damage
- cell proliferation
- computed tomography
- magnetic resonance
- long non coding rna
- cell cycle arrest
- risk assessment
- magnetic resonance imaging
- signaling pathway
- small molecule
- high resolution
- protein protein
- cell death
- drug delivery
- endoplasmic reticulum stress