Cho Hyok-Rae, Son Yonghae, Kim Sun-Mi, Kim Bo-Young, Eo Seong-Kug, Park Young Chul, Kim Koanhoi
Department of Neurosurgery, Kosin University, College of Medicine, Seo-gu, Busan, Republic of Korea.
Department of Pharmacology, Pusan National University-School of Medicine, Yangsan, Gyeongnam, Republic of Korea.
PLoS One. 2017 Mar 21;12(3):e0173749. doi: 10.1371/journal.pone.0173749. eCollection 2017.
We investigated effects of 7-oxygenated cholesterol derivatives present in atherosclerotic lesions, 7α-hydroxycholesterol (7αOHChol), 7β-hydroxycholesterol (7βOHChol), and 7-ketocholesterol (7K), on IL-8 expression. Transcript levels of IL-8 and secretion of its corresponding gene product by monocytes/macrophages were enhanced by treatment with 7αOHChol and, to a lesser extent, 7K, but not by 7βOHChol. The 7-oxygenated cholesterol derivatives, however, did not change transcription of the IL-8 gene in vascular smooth muscle cells. 7αOHChol-induced IL-8 gene transcription was inhibited by cycloheximide and Akt1 downregulation, but not by OxPAPC. Expression of C5a receptor was upregulated after stimulation with 7αOHChol, but not with 7K and 7βOHChol, and a specific antagonist of C5a receptor inhibited 7αOHChol-induced IL-8 gene expression in a dose dependent manner. Pharmacological inhibitors of PI3K and MEK almost completely inhibited expression of both IL-8 and cell-surface C5a receptor induced by 7αOHChol. These results indicate that 7-oxygenated cholesterol derivatives have differential effects on monocyte/macrophage expression of IL-8 and C5a receptor and that C5a receptor is involved in 7αOHChol-induced IL-8 expression via PI3K and MEK.
我们研究了动脉粥样硬化病变中存在的7-氧化胆固醇衍生物,即7α-羟基胆固醇(7αOHChol)、7β-羟基胆固醇(7βOHChol)和7-酮胆固醇(7K)对白细胞介素-8(IL-8)表达的影响。用7αOHChol处理可增强单核细胞/巨噬细胞中IL-8的转录水平及其相应基因产物的分泌,7K在较小程度上也有此作用,但7βOHChol则无此作用。然而,这些7-氧化胆固醇衍生物并未改变血管平滑肌细胞中IL-8基因的转录。7αOHChol诱导的IL-8基因转录受到放线菌酮和Akt1下调的抑制,但不受氧化型磷脂酰胆碱(OxPAPC)的抑制。用7αOHChol刺激后,C5a受体的表达上调,但7K和7βOHChol刺激后则未上调,并且C5a受体的特异性拮抗剂以剂量依赖性方式抑制7αOHChol诱导的IL-8基因表达。磷脂酰肌醇-3激酶(PI3K)和丝裂原活化蛋白激酶(MEK)的药理抑制剂几乎完全抑制了7αOHChol诱导的IL-8和细胞表面C5a受体的表达。这些结果表明,7-氧化胆固醇衍生物对单核细胞/巨噬细胞中IL-8和C5a受体的表达具有不同的影响,并且C5a受体通过PI3K和MEK参与7αOHChol诱导的IL-8表达。