Derhamnosylmaysin Inhibits Adipogenesis via Inhibiting Expression of PPARγ and C/EBPα in 3T3-L1 Cells

We investigated the effects of derhamnosylmaysin (DM) on adipogenesis and lipid accumulation in 3T3-L1 adipocytes. Our data showed that DM inhibited lipid accumulation and adipocyte differentiation in 3T3-L1 cells. Treatment of 3T3-L1 adipocytes with DM decreased the expression of major transcriptio...

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Main Authors: Hang-Hee Cho, Sun-Hee Jang, Chungkil Won, Chung-Hui Kim, Hong-Duck Kim, Tae Hoon Kim, Jae-Hyeon Cho
Format: Article
Language:English
Published: MDPI AG 2022-06-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/27/13/4232
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author Hang-Hee Cho
Sun-Hee Jang
Chungkil Won
Chung-Hui Kim
Hong-Duck Kim
Tae Hoon Kim
Jae-Hyeon Cho
author_facet Hang-Hee Cho
Sun-Hee Jang
Chungkil Won
Chung-Hui Kim
Hong-Duck Kim
Tae Hoon Kim
Jae-Hyeon Cho
author_sort Hang-Hee Cho
collection DOAJ
description We investigated the effects of derhamnosylmaysin (DM) on adipogenesis and lipid accumulation in 3T3-L1 adipocytes. Our data showed that DM inhibited lipid accumulation and adipocyte differentiation in 3T3-L1 cells. Treatment of 3T3-L1 adipocytes with DM decreased the expression of major transcription factors, such as sterol regulatory element-binding protein-1c (SREBP-1c), the CCAAT-enhancer-binding protein (CEBP) family, and peroxisome proliferator-activated receptor gamma (PPARγ), in the regulation of adipocyte differentiation. Moreover, the expression of their downstream target genes related to adipogenesis and lipogenesis, including adipocyte fatty acid-binding protein (aP2), lipoprotein lipase (LPL), stearyl-CoA-desaturase-1 (SCD-1), acetyl-CoA carboxylase (ACC), and fatty acid synthase (FAS), was also decreased by treatment with DM during adipogenesis. Additionally, DM attenuated insulin-stimulated phosphorylation of Akt. These results first demonstrated that DM inhibited adipogenesis and lipogenesis through downregulation of the key adipogenic transcription factors SREBP-1c, the CEBP family, and PPARγ and inactivation of the major adipogenesis signaling factor Akt, which is intermediated in insulin. These studies demonstrated that DM is a new bioactive compound for antiadipogenic reagents for controlling overweight and obesity.
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spelling doaj.art-7eae657ef711475a9ca682e4173cebf82023-12-03T14:13:58ZengMDPI AGMolecules1420-30492022-06-012713423210.3390/molecules27134232Derhamnosylmaysin Inhibits Adipogenesis via Inhibiting Expression of PPARγ and C/EBPα in 3T3-L1 CellsHang-Hee Cho0Sun-Hee Jang1Chungkil Won2Chung-Hui Kim3Hong-Duck Kim4Tae Hoon Kim5Jae-Hyeon Cho6Institute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, KoreaInstitute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, KoreaInstitute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, KoreaInstitute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, KoreaDepartment of Public Health, Division of Environmental Health Science, New York Medical College, Valhalla, NY 10595, USADepartment of Food Science and Biotechnology, Daegu University, Gyungsan 38453, KoreaInstitute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, KoreaWe investigated the effects of derhamnosylmaysin (DM) on adipogenesis and lipid accumulation in 3T3-L1 adipocytes. Our data showed that DM inhibited lipid accumulation and adipocyte differentiation in 3T3-L1 cells. Treatment of 3T3-L1 adipocytes with DM decreased the expression of major transcription factors, such as sterol regulatory element-binding protein-1c (SREBP-1c), the CCAAT-enhancer-binding protein (CEBP) family, and peroxisome proliferator-activated receptor gamma (PPARγ), in the regulation of adipocyte differentiation. Moreover, the expression of their downstream target genes related to adipogenesis and lipogenesis, including adipocyte fatty acid-binding protein (aP2), lipoprotein lipase (LPL), stearyl-CoA-desaturase-1 (SCD-1), acetyl-CoA carboxylase (ACC), and fatty acid synthase (FAS), was also decreased by treatment with DM during adipogenesis. Additionally, DM attenuated insulin-stimulated phosphorylation of Akt. These results first demonstrated that DM inhibited adipogenesis and lipogenesis through downregulation of the key adipogenic transcription factors SREBP-1c, the CEBP family, and PPARγ and inactivation of the major adipogenesis signaling factor Akt, which is intermediated in insulin. These studies demonstrated that DM is a new bioactive compound for antiadipogenic reagents for controlling overweight and obesity.https://www.mdpi.com/1420-3049/27/13/4232adipogenesisAktderhamnosylmaysinlipogenesis3T3-L1 cells
spellingShingle Hang-Hee Cho
Sun-Hee Jang
Chungkil Won
Chung-Hui Kim
Hong-Duck Kim
Tae Hoon Kim
Jae-Hyeon Cho
Derhamnosylmaysin Inhibits Adipogenesis via Inhibiting Expression of PPARγ and C/EBPα in 3T3-L1 Cells
Molecules
adipogenesis
Akt
derhamnosylmaysin
lipogenesis
3T3-L1 cells
title Derhamnosylmaysin Inhibits Adipogenesis via Inhibiting Expression of PPARγ and C/EBPα in 3T3-L1 Cells
title_full Derhamnosylmaysin Inhibits Adipogenesis via Inhibiting Expression of PPARγ and C/EBPα in 3T3-L1 Cells
title_fullStr Derhamnosylmaysin Inhibits Adipogenesis via Inhibiting Expression of PPARγ and C/EBPα in 3T3-L1 Cells
title_full_unstemmed Derhamnosylmaysin Inhibits Adipogenesis via Inhibiting Expression of PPARγ and C/EBPα in 3T3-L1 Cells
title_short Derhamnosylmaysin Inhibits Adipogenesis via Inhibiting Expression of PPARγ and C/EBPα in 3T3-L1 Cells
title_sort derhamnosylmaysin inhibits adipogenesis via inhibiting expression of pparγ and c ebpα in 3t3 l1 cells
topic adipogenesis
Akt
derhamnosylmaysin
lipogenesis
3T3-L1 cells
url https://www.mdpi.com/1420-3049/27/13/4232
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