Repression of adipose vascular endothelial growth factor reduces obesity through adipose browning

Author:

Chen Yang1,Zhao Mingyue1,Zheng Tingting1,Adlat Salah1,Jin Honghong1,Wang Chenhao1,Li Dan1,Zaw Myint May Zun1,Yao Yapeng1,Xu Liu1,San Mingjun1,Wen Huaizhen1,Zhang Yuntao1,Lu Xiaodan1,Yang Ling2,Zhang Luqing13,Feng Xuechao13,Zheng Yaowu13

Affiliation:

1. Transgenic Research Center, Northeast Normal University, Changchun, China

2. Shanxi Medical University, Taiyuan, China

3. Key Laboratory of Molecular Epigenetics of Ministry of Education, Northeast Normal University, Changchun, China

Abstract

Obesity is the result of excessive energy accumulation and is associated with many diseases. We previously reported that universal repression of vascular endothelial growth factor (VEGF) leads to brown-like adipocyte development in white adipose tissues, and that these mice are resistant to obesity (Lu X et al. Endocrinology 153: 3123–3132, 2012). Using an adipose-specific VEGF repression mouse model (aP2-rtTR-krabtg/+/VEGFtetO/tetO), we show that adipose-specific VEGF repression can repeat the previous phenotypes, including adipose browning, increased energy consumption, and reduction in body weight. Expression of brown adipose-associated genes is increased, and white adipose-associated genes are downregulated under VEGF repression. Our study demonstrates that adipose-specific VEGF repression can lead to antiobesity activity through adipose browning and has potential clinical value.

Funder

National Natural Science Foundation of China (NSFC)

Natural Science Foundation of Jilin Province

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology,Endocrinology, Diabetes and Metabolism

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