Our study uncovers a dynamic immunoregulatory role of dermal white adipose tissue (dWAT) in the progression and resolution of neutrophilic skin inflammation in an imiquimod-induced psoriatic mouse model. Initially, dWAT undergoes lipolysis and expands preadipocytes (pAds) secreting CXCL1/SAA3 to recruit neutrophils, which amplify inflammation via IL1β and activate pAds through the IL1-NFκB-C/EBPδ pathway. Prolonged IL1β exposure triggers PPARγ-dependent differentiation of pAds into early adipocytes, producing anti-inflammatory lipids that resolve neutrophilic inflammation. We also observed a negative correlation between neutrophil-related inflammatory response with dermal lipogenesis is also observed in human psoriasis. These findings highlight dWAT as an immunomodulatory hub, suggesting adipogenic reprogramming or lipid delivery as novel psoriasis therapies.
- Tian Xia
- Wenlu Zhang
- Ling-juan Zhang