Abstract:【Abstract】 Objective To investigate the Effects of perfluorocarbon on the inflammatory reaction induced by LPS and the expression of single immunoglobin IL1 receptor related protein (SIGIRR) in alveolar epithelial cells (A549 cells). Methods The A549 cells were divided into four groups (normal cell group, PFC+LPS group, PFC group and LPS group). A549 cells of each group were incubated for 24 h, and then the culture supernatants, cellular total protein and cellular nuclear protein were collected. The levels of TNFα, IL6 and IL10 in the culture supernatants were detected by ELISA. The protein expression levels of NFκB p65 in nuclear extracts and the protein expression levels of SIGIRR in A549 cells of each group were also measured by Westernblot analysis. Results The results of ELISA demonstrated that the levels of TNFα and IL6 in LPS group were higher than those in normal cell group (P<005). Compared with LPS group, the levels of TNFα and IL6 in PFC+LPS group were significantly decreased (P<005). Meanwhile, the results of ELISA also demonstrated that the levels of IL10 in PFC+LPS group were higher than those in LPS group and PFC could promote IL10 secretion in A549 cells (P<005). The results of Westernblot analysis showed that the protein levels of phosphoNFκB p65 in LPS group were higher than those in normal cell group (P<005). Compared with LPS group, the protein levels of phosphoNFκB p65 in PFC+LPS group were significantly decreased (P<005). Moreover, the results of Westernblot analysis also showed that the protein levels of SIGIRR in PFC+LPS group were higher than those in LPS group and PFC could upregulate the expression of SIGIRR in A549 cells (P<005), conversely, LPS suppressed the expression of SIGIRR in A549 cells. Conclusion PFC could attenuate the LPSinduced inflammation in alveolar epithelial cells. Promotion of IL10 secretion and upregulaiton SIGIRR expression may the possible mechanism of PFC protection against LPSinduce inflammation in alveolar epithelial cells.