Forkhead Box i2 (Foxi2) Transcription Factor Regulates Systemic Energy Metabolism Via Neuropeptide AgRP

Author:

Fan Yatong1,Sheng Sufang1,Guo Cunle2,Qiao Wei1,Jin Yue3,Tan Lu4,Gao Yong5,Zhang Lei1,Dong Xi2,Zhang Jun6,Li Xiaorong7,Shen Hui89,Liao Yunfei10,Chang Yongsheng17

Affiliation:

1. 1Key Laboratory of Immune Microenvironment and Disease (Ministry of Education), Tianjin Key Laboratory of Cellular Homeostasis and Disease, Department of Physiology and Pathophysiology, Tianjin Medical University, Tianjin, China

2. 2Laboratory of Neurobiology, School of Biomedical Engineering, Tianjin Medical University, Tianjin, China

3. 3Tianjin Key Laboratory of Cellular and Molecular Immunology and Key Laboratory of the Educational Ministry of China, Department of Immunology, Tianjin Medical University, Tianjin, China

4. 4Department of Laboratory Animal Science, Tianjin Medical University, Tianjin, China

5. 5Science and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, China

6. 6Department of Basic Medicine, Shihezi University School of Medicine, Shihezi, Xinjiang, China

7. 7Tianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin, China

8. 8Department of Cell Biology, Tianjin Medical University, Tianjin, China

9. 9Brain Research Center of Innovation Institute of Traditional Chinese medicine, Shandong University of traditional Chinese Medicine, Jinan, Shandong, China

10. 10Department of Endocrinology, Wuhan Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China

Abstract

The neuropeptide AgRP is essential for maintaining systemic energy homeostasis. In the present study, we show that hypothalamic Foxi2, as a novel regulator of nutrient sensing, controls systemic energy metabolism by specifically stimulating AgRP expression. Foxi2 was highly expressed in the hypothalamus, and its expression was induced by fasting. Immunofluorescence assays demonstrated that Foxi2 was localized in AgRP neurons. We stereotaxically injected AAV to selectively overexpress Foxi2 in AgRP-IRES-Cre mice and found that Foxi2 overexpression in AgRP neurons specifically increased AgRP expression, thereby increasing food intake and reducing energy expenditure, subsequently leading to obesity and insulin resistance. Mechanistically, Foxi2 stimulated AgRP expression by directly binding to it and activating its transcription. Furthermore, Foxi2 overexpression activated AgRP neuron activity, as revealed by whole-cell patch-clamp experiments. Conversely, global Foxi2 mutant mice became leaner with age and were resistant to high-fat diet (HFD)–induced obesity and metabolic disturbances. Collectively, our data suggest that Foxi2 plays an important role in controlling energy metabolism by regulating AgRP expression.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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