Amelogenins modulate cytokine expression in LPS-challenged cultured human macrophages

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• 作者：Sofia Almqvist^a ; ^b ; ^c ; ^{sofia.almqvist@biomaterials.gu.se} ; Maria Werthé ; n^b ; ^c ; S. Petter Lyngstadaas^d ; Christina Gretzer^a ; ^e ; Peter Thomsen^a ; ^b ; ^f
• 关键词：Amelogenins ; Extracellular matrix (ECM) ; Macrophage ; Inflammation ; Cytokine
• 刊名：Cytokine
• 出版年：2012
• 期刊代码：97_10434666
• 类别：imm
• 出版时间：May, 2012
• 卷：58
• 期：2
• 页码：274-279
• 文件大小：444 K

摘要

Amelogenins are enamel matrix proteins with a proven ability to restore tissues in patients with advanced periodontitis and chronic skin wounds. To explore the mechanisms of action of amelogenins in wound inflammation, the in vitro effect on the expression of selected cell mediators involved in inflammation and tissue repair from human monocyte-derived macrophages was studied. Macrophages were treated with amelogenins in serum-enriched medium with simultaneous lipopolysaccharide (LPS) stimulation, for 6, 24 and 72 h, and the conditioned culture medium was analysed for 28 different cytokines. Amelogenin treatment directed the LPS-induced release of both pro- and anti-inflammatory cytokines towards an alternatively activated macrophage phenotype. This change in activation was also demonstrated by the amelogenin-induced secretion of alternative macrophage activation-associated CC chemokine-1 (AMAC-1, also known as CCL18; p < 0.001), a well-documented marker of alternative activation. Amelogenins were also shown significantly to increase the macrophage expression of vascular endothelial growth factor and, to a lesser but significant extent, insulin-like growth factor-1 after 24 h of culture. The results of the present in vitro study show that monocyte-derived macrophages stimulated by inflammatory agonist LPS respond to the treatment with amelogenins by reducing the pro-inflammatory activity and increasing the expression of tissue repair mediators.