Laos Sirle, Baeckström Dan, Hansson Gunnar C
Department of Medical Biochemistry, Göteborg University, 413 90 Gothenburg, Sweden.
Int J Oncol. 2006 Mar;28(3):695-704.
CD43 is a heavily O-glycosylated type I trans-membrane protein, expressed at high levels on the surface of leukocytes. It is frequently overexpressed in early colon adenomas, but not in normal colon epithelial cells. To identify CD43 target genes, gene array analysis was performed using a tetracycline-inducible CD43 expression system in human colon adenocarcinoma SW480 cells. CD43 was demonstrated to down-regulate a variety of chemokine genes. Overexpression of CD43 suppressed constitutive as well as PMA-induced NF-kappaB activation and reduced the DNA binding of transcription factor p65 but not p50. Furthermore, a reduced NF-kappaB responsive promoter activity was observed and a decreased expression of proinflammatory chemokines MCP-1, IL-8 and GRO-alpha. These results suggest that overexpression of CD43 suppresses a subset of NF-kappaB target genes, partly via the inhibition of p65 transcriptional activity.
CD43是一种高度O-糖基化的I型跨膜蛋白,在白细胞表面高水平表达。它在早期结肠腺瘤中经常过度表达,但在正常结肠上皮细胞中不表达。为了鉴定CD43的靶基因,在人结肠腺癌SW480细胞中使用四环素诱导的CD43表达系统进行了基因阵列分析。结果表明,CD43可下调多种趋化因子基因。CD43的过表达抑制了组成型以及佛波酯(PMA)诱导的核因子κB(NF-κB)激活,并降低了转录因子p65而非p50的DNA结合能力。此外,还观察到NF-κB反应性启动子活性降低,以及促炎趋化因子单核细胞趋化蛋白-1(MCP-1)、白细胞介素-8(IL-8)和生长调节致癌基因-α(GRO-α)的表达减少。这些结果表明,CD43的过表达部分通过抑制p65的转录活性来抑制NF-κB靶基因的一个子集。