| Macrophage CREBZF Orchestrates Inflammatory Response to Potentiate Insulin Resistance and Type 2 Diabetes | |
| 論文作者 | Liu, YX; Su, WT; Liu, ZS; Hu, ZM; Shen, JX; Zheng, ZP; Ding, D; Huang, W; Li, WJ; Cai, GX; Wei, S; Li, N; Fang, X; Li, H; Qin, J; Zhang, HB; Xiao, YC; Bi, Y; Cui, AY; Zhang, CX; Li, Y |
| 期刊/會議名稱 | ADVANCED SCIENCE |
| 論文年度 | 2024 |
| 論文類別 | |
| 摘要 | Chronic adipose tissue inflammation accompanied by macrophage accumulation and activation is implicated in the pathogenesis of insulin resistance and type 2 diabetes in humans. The transcriptional coregulator CREBZF is a key factor in hepatic metabolism, yet its role in modulating adipose tissue inflammation and type 2 diabetes remains elusive. The present study demonstrates that overnutrition-induced CREBZF links adipose tissue macrophage (ATM) proinflammatory activation to insulin resistance. CREBZF deficiency in macrophages, not in neutrophils, attenuates macrophage infiltration in adipose, proinflammatory activation, and hyperglycemia in diet-induced insulin-resistant mice. The coculture assays show that macrophage CREBZF deficiency improves insulin sensitivity in primary adipocytes and adipose tissue. Mechanistically, CREBZF competitively inhibits the binding of I kappa B alpha to p65, resulting in enhanced NF-kappa B activity. In addition, bromocriptine is identified as a small molecule inhibitor of CREBZF in macrophages, which suppresses the proinflammatory phenotype and improves metabolic dysfunction. Furthermore, CREBZF is highly expressed in ATM of obese humans and mice, which is positively correlated with proinflammatory genes and insulin resistance in humans. This study identifies a previously unknown role of CREBZF coupling ATM activation to systemic insulin resistance and type 2 diabetes. |
| 期 | 13 |
| 卷 | 11 |
| 影響因子 | 14.3 |
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