Eriocalyxin B Inhibits Adipogenesis in 3T3-L1 Adipocytes by Cell Cycle Arrest

被引:14
作者
Mu, Rong-Fang [1 ,4 ]
Niu, Yan-Fen [3 ]
Wang, Qian [1 ,4 ]
Zhou, Hui-Min [1 ,4 ]
Hu, Jing [1 ]
Qin, Wan-Ying [1 ,4 ]
Xiong, Wen-Yong [1 ,2 ,4 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China
[2] Yunnan Univ, Key Lab Med Chem Nat Resource, Kunming 650500, Yunnan, Peoples R China
[3] Kunming Med Univ, Biomed Engn Res Ctr, Kunming 650500, Yunnan, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
国家重点研发计划;
关键词
Eriocalyxin B; Adipocyte differentiation; Cell cycle; TRANSCRIPTIONAL REGULATION; OBESITY; APOPTOSIS; DIFFERENTIATION; GENE; BETA;
D O I
10.1007/s13659-020-00240-6
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Eriocalyxin B, an ent-Kaurene diterpenoid extracted from a traditional Chinese herb Isodon eriocalyx, has been shown to possess multifunctional activities such as anti-cancer and anti-inflammatory. However, the function and mechanism of the compound in adipocyte differentiation is still unknown. Here we reported that eriocalyxin B blunted adipogenesis remarkably by inhibiting the accumulation of lipid droplets, triglycerides and the expressions of adipogenesis-related factors, including C/EBP beta, C/EBP alpha, PPAR gamma, and FABP4. Moreover, we showed that the inhibition might be the consequence of cell cycle being arrested at the G2/M phase during the mitotic clonal expansion of adipocyte differentiation, most likely by suppressing mRNAs and proteins of CDK1, CDK2, Cyclin A and Cyclin B1. Overall, we conclude that eriocalyxin B is capable of inhibiting adipocyte differentiation at the early stage through downregulating the proteins involved in cell cycle progression.
引用
收藏
页码:131 / 140
页数:10
相关论文
共 40 条
[1]  
Ahn J, 2008, BIOCHEM BIOPH RES CO, V404, P579
[2]   Obesity perceptions and documentation among primary care clinicians at a rural academic center [J].
Aleem, Sohaib ;
Lasky, Rosalind ;
Brook, W. Blair ;
Batsis, John A. .
OBESITY RESEARCH & CLINICAL PRACTICE, 2015, 9 (04) :408-415
[3]   Overweight, obesity and cancer: Epidemiological evidence and proposed mechanisms [J].
Calle, EE ;
Kaaks, R .
NATURE REVIEWS CANCER, 2004, 4 (08) :579-591
[4]   EriB targeted inhibition of microglia activity attenuates MPP+ induced DA neuron injury through the NF-B signaling pathway [J].
Dou, Fangfang ;
Chu, Xinkun ;
Zhang, Bei ;
Liang, Liang ;
Lu, Guoqiang ;
Ding, Jianqing ;
Chen, Shengdi .
MOLECULAR BRAIN, 2018, 11
[5]   Obesity [J].
Gonzalez-Muniesa, Pedro ;
Martinez-Gonzalez, Miguel-Angel ;
Hu, Frank B. ;
Despres, Jean-Pierre ;
Matsuzawa, Yuji ;
Loos, Ruth J. F. ;
Moreno, Luis A. ;
Bray, GeorgeA. ;
Alfredo Martinez, J. .
NATURE REVIEWS DISEASE PRIMERS, 2017, 3
[6]   Daidzein reduces the proliferation and adiposeness of 3T3-L1 preadipocytes via regulating adipogenic gene expression [J].
He, Yang ;
Niu, Wenjing ;
Xia, Chuanqi ;
Cao, Binghai .
JOURNAL OF FUNCTIONAL FOODS, 2016, 22 :446-453
[7]   Adenanthin, a Natural ent-Kaurane Diterpenoid Isolated from the Herb Isodon adenantha Inhibits Adipogenesis and the Development of Obesity by Regulation of ROS [J].
Hu, Jing ;
Li, Xingren ;
Tian, Weifeng ;
Lu, Yanting ;
Xu, Yuhui ;
Wang, Fang ;
Qin, Wanying ;
Ma, Xiuli ;
Puno, Pema-Tenzin ;
Xiong, Wenyong .
MOLECULES, 2019, 24 (01)
[8]   Polymeric Carriers for Controlled Drug Delivery in Obesity Treatment [J].
Huang, Di ;
Deng, Meng ;
Kuang, Shihuan .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2019, 30 (12) :974-989
[9]  
Hwang LC, 2012, ASIA PAC J CLIN NUTR, V21, P227
[10]   Cell Models and Their Application for Studying Adipogenic Differentiation in Relation to Obesity: A Review [J].
Javier Ruiz-Ojeda, Francisco ;
Iris Ruperez, Azahara ;
Gomez-Llorente, Carolina ;
Gil, Angel ;
Maria Aguilera, Concepcion .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (07)