Abstract

Abstract Blimp-1, encoded by Prdm1, is a master transcriptional factor that governs the differentiation fate of many cell types, including epidermal keratinocytes. Previous results from our laboratory showed that inducible deletion of Prdm1 in mouse epidermis spontaneously induces skin inflammation. Epidermis composes of not only epidermal keratinocytes, but also epidermal appendages, including hair follicles, sebaceous glands and sweat glands. Sebaceous glands release the “oil” contents that lubricate the skin. Our previous results also showed that Blimp-1 is required for the maintenance of the homeostasis of terminally differentiated sebocytes. Here, we aim to investigate the potential function of Blimp-1 in inflammation and lipid metabolism in sebocytes. We depleted Blimp-1 by siRNA in SZ95, the immortalized human sebocyte cells. We found accumulated and enlarged lipid droplets in Blimp-1 depleted cells. Consistently, gas chromatography–mass spectrometry (GC-MS) analyses showed that the levels of several long-chain fatty acids, including 1,3-dipalmitoyl-2oleoylglycerol, 1-palmitoyl-2oleoyl-3-lineoleoyl-rac-glycerol, and triolein, were accumulated in Blimp-1-depleted SZ95 cells, linking with the significant increases in the production of pro-inflammatory cytokines, including IL-1β, IL-6, IL-8 and IL-18. Thus, Blimp-1 served as a pivotal mediator in the regulation of the inflammatory responses in epidermis, likely also through affecting the lipid metabolism and cytokine production in sebocytes.

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