Transcription factor 4 (TCF-4) was recently identified as a candidate gene for the cause of type 2 diabetes, although the mechanisms have not been fully elucidated. In the present study, we demonstrated that the TCF-4 transgene in macrophages aggravated high-fat diet (HFD)-induced insulin resistance and chronic inflammation, characterized by the elevation of proinflammatory cytokines in the blood, liver and white adipose tissue, as well as a proinflammatory profile of immune cells in visceral fats in mice. Mechanistically, TCF-4 functioned as a co-activator of p65 to amplify the saturated free fatty acid (FFA)-stimulated promoter activity, mRNA transcription and secretion of proinflammatory cytokines in primary macrophages. Blockage of p65 with a specific interfering RNA or inhibitor could prevent TCF-4-enhanced expression of proinflammatory cytokines in FFA/lipopolysaccharide-treated primary macrophages. The p65 inhibitor could abolish macrophage TCF-4 transgene-aggravated systemic inflammation, glucose intolerance and insulin resistance in HFD-treated mice. In addition, we demonstrated that the mRNA expression of TCF-4 in the peripheral blood monocytes from humans was positively correlated to the levels of interleukin (IL)-1β, tumour necrosis factor α, IL-6 and fasting plasma glucose. In summary, we identified TCF-4 as a co-activator of p65 in the potentiation of proinflammatory cytokine production in macrophages and aggravation of HFD-induced chronic inflammation and insulin resistance in mice.
Macrophage TCF-4 co-activates p65 to potentiate chronic inflammation and insulin resistance in mice
- Views Icon Views
- Share Icon Share
- Cite Icon Cite
Xia Kang, Along Hou, Rui Wang, Da Liu, Wei Xiang, Qingyun Xie, Bo Zhang, Lixia Gan, Wei Zheng, Hongming Miao; Macrophage TCF-4 co-activates p65 to potentiate chronic inflammation and insulin resistance in mice. Clin Sci (Lond) 1 July 2016; 130 (14): 1257–1268. doi: https://doi.org/10.1042/CS20160192
Download citation file: