Glucocorticoids increase adiposity by stimulating Krüppel-like factor 9 expression in macrophages.
Yinliang ZhangChunyuan DuWei WangWei QiaoYuhui LiYujie ZhangSufang ShengXuenan ZhouLei ZhangHeng FanYing YuYong ChenYunfei LiaoShihong ChenYongsheng ChangPublished in: Nature communications (2024)
The mechanisms underlying glucocorticoid (GC)-induced obesity are poorly understood. Macrophages are the primary targets by which GCs exert pharmacological effects and perform critical functions in adipose tissue homeostasis. Here, we show that macrophages are essential for GC-induced obesity. Dexamethasone (Dex) strongly induced Krüppel-like factor 9 (Klf9) expression in macrophages. Similar to Dex, lentivirus-mediated Klf9 overexpression inhibits M1 and M2a markers expression, causing macrophage deactivation. Furthermore, the myeloid-specific Klf9 transgene promotes obesity. Conversely, myeloid-specific Klf9-knockout (mKlf9KO) mice are lean. Moreover, myeloid Klf9 knockout largely blocks obesity induced by chronic GC treatment. Mechanistically, GC-inducible KLF9 recruits the SIN3A/HDAC complex to the promoter regions of Il6, Ptgs2, Il10, Arg1, and Chil3 to inhibit their expression, subsequently reducing thermogenesis and increasing lipid accumulation by inhibiting STAT3 signaling in adipocytes. Thus, KLF9 in macrophages integrates the beneficial anti-inflammatory and adverse metabolic effects of GCs and represents a potential target for therapeutic interventions.
Keyphrases
- insulin resistance
- adipose tissue
- high fat diet induced
- transcription factor
- poor prognosis
- metabolic syndrome
- weight loss
- weight gain
- type diabetes
- high glucose
- bone marrow
- dendritic cells
- anti inflammatory
- diabetic rats
- cell proliferation
- acute myeloid leukemia
- drug induced
- gene expression
- binding protein
- long non coding rna
- skeletal muscle
- physical activity
- body mass index
- climate change
- body composition
- mass spectrometry
- gas chromatography
- immune response
- high dose
- simultaneous determination
- wild type
- adverse drug
- histone deacetylase