LAUSR

ABSTRACT Crosstalk occurs between dyslipidemia and chronic inflammation, which are both precipitants of atherosclerosis. Sterol regulatory element binding proteins cleavage‐activating protein (SCAP) plays a key role in regulating cholesterol homeostasis. The present study investigated the effects of SCAP dysfunction on the expression of inflammatory cytokines and lipid metabolism in THP‐1 macrophages. Intracellular cholesterol content was assessed by Oil Red O staining and quantitative assays. The expression of SCAP, HMGCR, pro‐IL‐1&bgr; and N‐SREBP2, p65(N) in the nucleus were examined by real‐time quantitative RT‐PCR and Western blotting. The level of secretary proteins IL‐1&bgr;, TNF‐&agr; and MCP‐1 in the supernatants were determined by ELISA. The translocation of SCAP from the endoplasmic reticulum (ER) to the Golgi was detected by confocal microscopy. Our results demonstrated that over‐expression of SCAP significantly increased the expression of HMGCR, pro‐IL‐1&bgr; in the cytoplasm, and mature IL‐1&bgr;, TNF‐&agr;, MCP‐1 in the supernatants, while knocking down SCAP dramatically decreased the expression of these molecules. Betulin effectively suppressed the accumulation of intracellular cholesterol in the SCAP over‐expressed THP‐1 macrophages, but did not affect the expression of inflammatory cytokines, indicating that the pro‐inflammatory effect of SCAP was independent of its routine role in regulating cholesterol homeostasis. Furthermore, we investigated the molecular mechanisms mediating the crosstalk between dyslipidemia and inflammatory responses. Knocking down SCAP attenuated LPS‐induced I&kgr;B phosphorylation and reduced the nuclear level of p65, while over‐expression of SCAP increased the nuclear level of p65. Knocking down p65 abolished the proinflammatory effect represented by elevated expression of the inflammatory mediators in the SCAP over‐expressed THP‐1 macrophages, suggesting that SCAP dysfunction stimulated inflammatory responses via activating the NF‐&kgr;B signaling pathway. In conclusion, the cholesterol sensor SCAP plays a role in regulating the expression of inflammatory factors such as IL‐1&bgr;, TNF‐&agr;, and MCP‐1 in THP‐1 macrophages. SCAP mediates the inflammatory response via activating the NF‐&kgr;B pathway. This new function of SCAP is independent of its role in lipid metabolism. HIGHLIGHTSThe dysfunction of SCAP interplays with inflammatory responses.The effect above is independent of SCAP's well‐known role in regulating cholesterol homeostasis.The dysfunction of SCAP mediated the activation of NF‐&kgr;B signaling pathway.