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Ellagic Acid Reduces Adipogenesis through Inhibition of Differentiation-Prevention of the Induction of Rb Phosphorylation in 3T3-L1 Adipocytes

Ellagic acid (EA) present in many fruits and nuts serves as antiproliferation, anti-inflammatory, and antitumorigenic properties. However, the effect of EA on preadipocytes adipogenesis and its mechanism(s) have not been elucidated. The present study was designed to examine the effect of EA on adipo...

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Autores principales: Wang, Lifeng, Li, Linlin, Ran, Xinjian, Long, Mei, Zhang, Minfang, Tao, Yicun, Luo, Xin, Wang, Ye, Ma, Xiaoli, Halmurati, Upur, Mao, Xinmin, Ren, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835195/
https://www.ncbi.nlm.nih.gov/pubmed/24302962
http://dx.doi.org/10.1155/2013/287534
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author Wang, Lifeng
Li, Linlin
Ran, Xinjian
Long, Mei
Zhang, Minfang
Tao, Yicun
Luo, Xin
Wang, Ye
Ma, Xiaoli
Halmurati, Upur
Mao, Xinmin
Ren, Jun
author_facet Wang, Lifeng
Li, Linlin
Ran, Xinjian
Long, Mei
Zhang, Minfang
Tao, Yicun
Luo, Xin
Wang, Ye
Ma, Xiaoli
Halmurati, Upur
Mao, Xinmin
Ren, Jun
author_sort Wang, Lifeng
collection PubMed
description Ellagic acid (EA) present in many fruits and nuts serves as antiproliferation, anti-inflammatory, and antitumorigenic properties. However, the effect of EA on preadipocytes adipogenesis and its mechanism(s) have not been elucidated. The present study was designed to examine the effect of EA on adipogenesis in 3T3-L1 preadipocytes and underlying mechanism(s) of action involved. Data show that EA administration decreased the accumulation of lipid droplets. The inhibition was diminished when the addition of EA was delayed to days 2–4 of differentiation. Clonal expansion was reduced in the presence of EA. FACS analysis showed that EA blocked the cell cycle at the G1/S transition. EdU incorporation also confirmed that EA refrained cell from entering S phase. Our data also revealed that the differentiation-induced protein expression of Cyclin A and phosphorylation of the retinoblastoma protein (Rb) were impaired by EA. Differentiation-dependent expression and DNA-binding ability of C/EBPα were also inhibited by EA. Alterations in cell cycle-associated proteins may be important with respect to the antiadipogenic action of EA. In conclusion, EA is capable of inhibiting adipogenesis in 3T3-L1 adipocytes possibly through reduction of Cyclin A protein expression and Rb phosphorylation. With the blocking of G1/S phase transition, EA suppresses terminal differentiation and lipid accumulation in 3T3-L1 adipocytes.
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spelling pubmed-38351952013-12-03 Ellagic Acid Reduces Adipogenesis through Inhibition of Differentiation-Prevention of the Induction of Rb Phosphorylation in 3T3-L1 Adipocytes Wang, Lifeng Li, Linlin Ran, Xinjian Long, Mei Zhang, Minfang Tao, Yicun Luo, Xin Wang, Ye Ma, Xiaoli Halmurati, Upur Mao, Xinmin Ren, Jun Evid Based Complement Alternat Med Research Article Ellagic acid (EA) present in many fruits and nuts serves as antiproliferation, anti-inflammatory, and antitumorigenic properties. However, the effect of EA on preadipocytes adipogenesis and its mechanism(s) have not been elucidated. The present study was designed to examine the effect of EA on adipogenesis in 3T3-L1 preadipocytes and underlying mechanism(s) of action involved. Data show that EA administration decreased the accumulation of lipid droplets. The inhibition was diminished when the addition of EA was delayed to days 2–4 of differentiation. Clonal expansion was reduced in the presence of EA. FACS analysis showed that EA blocked the cell cycle at the G1/S transition. EdU incorporation also confirmed that EA refrained cell from entering S phase. Our data also revealed that the differentiation-induced protein expression of Cyclin A and phosphorylation of the retinoblastoma protein (Rb) were impaired by EA. Differentiation-dependent expression and DNA-binding ability of C/EBPα were also inhibited by EA. Alterations in cell cycle-associated proteins may be important with respect to the antiadipogenic action of EA. In conclusion, EA is capable of inhibiting adipogenesis in 3T3-L1 adipocytes possibly through reduction of Cyclin A protein expression and Rb phosphorylation. With the blocking of G1/S phase transition, EA suppresses terminal differentiation and lipid accumulation in 3T3-L1 adipocytes. Hindawi Publishing Corporation 2013 2013-11-04 /pmc/articles/PMC3835195/ /pubmed/24302962 http://dx.doi.org/10.1155/2013/287534 Text en Copyright © 2013 Lifeng Wang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Lifeng
Li, Linlin
Ran, Xinjian
Long, Mei
Zhang, Minfang
Tao, Yicun
Luo, Xin
Wang, Ye
Ma, Xiaoli
Halmurati, Upur
Mao, Xinmin
Ren, Jun
Ellagic Acid Reduces Adipogenesis through Inhibition of Differentiation-Prevention of the Induction of Rb Phosphorylation in 3T3-L1 Adipocytes
title Ellagic Acid Reduces Adipogenesis through Inhibition of Differentiation-Prevention of the Induction of Rb Phosphorylation in 3T3-L1 Adipocytes
title_full Ellagic Acid Reduces Adipogenesis through Inhibition of Differentiation-Prevention of the Induction of Rb Phosphorylation in 3T3-L1 Adipocytes
title_fullStr Ellagic Acid Reduces Adipogenesis through Inhibition of Differentiation-Prevention of the Induction of Rb Phosphorylation in 3T3-L1 Adipocytes
title_full_unstemmed Ellagic Acid Reduces Adipogenesis through Inhibition of Differentiation-Prevention of the Induction of Rb Phosphorylation in 3T3-L1 Adipocytes
title_short Ellagic Acid Reduces Adipogenesis through Inhibition of Differentiation-Prevention of the Induction of Rb Phosphorylation in 3T3-L1 Adipocytes
title_sort ellagic acid reduces adipogenesis through inhibition of differentiation-prevention of the induction of rb phosphorylation in 3t3-l1 adipocytes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835195/
https://www.ncbi.nlm.nih.gov/pubmed/24302962
http://dx.doi.org/10.1155/2013/287534
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