APE1/Ref-1 Inhibits Adipogenic Transcription Factors during Adipocyte Differentiation in 3T3-L1 Cells
Apurinic/apyrimidinic endonuclease 1/redox factor-1 ( ) is a multifunctional protein involved in DNA repair and redox regulation. The redox activity of is involved in inflammatory responses and regulation of DNA binding of transcription factors related to cell survival pathways. However, the effect...
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Published in | International journal of molecular sciences Vol. 24; no. 4; p. 3251 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
07.02.2023
MDPI |
Subjects | |
Online Access | Get full text |
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Summary: | Apurinic/apyrimidinic endonuclease 1/redox factor-1 (
) is a multifunctional protein involved in DNA repair and redox regulation. The redox activity of
is involved in inflammatory responses and regulation of DNA binding of transcription factors related to cell survival pathways. However, the effect of
on adipogenic transcription factor regulation remains unknown. In this study, we investigated the effect of
on the regulation of adipocyte differentiation in 3T3-L1 cells. During adipocyte differentiation,
expression significantly decreased with the increased expression of adipogenic transcription factors such as CCAAT/enhancer binding protein (
)-
and peroxisome proliferator-activated receptor (
)-
, and the adipocyte differentiation marker adipocyte protein 2 (
) in a time-dependent manner. However,
overexpression inhibited
,
and
expression, which was upregulated during adipocyte differentiation. In contrast, silencing
or redox inhibition of
using E3330 increased the mRNA and protein levels of
,
, and
during adipocyte differentiation. These results suggest that
inhibits adipocyte differentiation by regulating adipogenic transcription factors, suggesting that
is a potential therapeutic target for regulating adipocyte differentiation. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1422-0067 1661-6596 1422-0067 |
DOI: | 10.3390/ijms24043251 |