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Delphinidin, a major anthocyanin, inhibits 3T3-L1 pre-adipocyte differentiation through activation of Wnt/beta-catenin signaling

Authors
Rahman, NaimurJeon, MisoKim, Yong-Sik
Issue Date
Jan-2016
Publisher
International Union of Biochemistry by IRL Press
Keywords
delphinidin; 3T3-L1; adipogenesis; wnt/beta-catenin; obesity
Citation
BioFactors, v.42, no.1, pp 49 - 59
Pages
11
Journal Title
BioFactors
Volume
42
Number
1
Start Page
49
End Page
59
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/9472
DOI
10.1002/biof.1251
ISSN
0951-6433
1872-8081
Abstract
Delphinidin (Del) is a major anthocyanin that is widely found in pigmented fruits and vegetables. Herein, we investigated the antiadipogenic effect and the molecular mechanism by which Del affects 3T3-L1 preadipocyte differentiation. We found that Del effectively reduced intracellular lipid accumulation and promoted lipolysis while regulating the expression of adipogenic transcription factors and their target genes. This lipid lowering effect of Del was largely limited to the early phase of adipogenesis, which is governed by the delayed cell cycle progression due to G(1) cell cycle arrest. Subsequently, Del suppressed the expression of early adipogenic transcription factors, such as C/EBP and C/EBP, as well as that of intermediate markers, C/EBP, PPAR, and the PPAR-target adipocyte markers adiponectin and aP2 (FABP4). Furthermore, Del treatment activated Wnt1, Wnt10b, the Wnt receptor Fzd2, and the coreceptors Lrp5/6, while it inactivated Gsk3, a member of the -catenin destruction complex. Moreover, Del treatment stabilized cytoplasmic -catenin levels and promoted its nuclear translocation, with subsequent activation of the expression of its downstream target genes, c-Myc and cyclin D1. Our findings therefore suggest that Del can effectively inhibit adipogenesis followed by the stabilization of -catenin during early 3T3-L1 differentiation via inhibition of its destructive complexes and activation of Wnt signaling, and may thus be a promising candidate for the prevention of metabolic diseases, including obesity. (c) 2016 BioFactors, 42(1):49-59, 2016
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