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Early gene expression analyzed by cDNA microarray and real-time PCR in osteoblasts cultured with chitosan monomer

机译:cDNA芯片和实时荧光定量PCR分析壳聚糖单体培养成骨细胞的早期基因表达

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Chitosan has a variety of biological activities. Although it has been reported that chitosan promotes osteogenesis in bone lesions, little is known about how it modulates the hard tissue forming cells at the gene level. This study focused on gene expressions in osteoblasts cultured with a super-low concentration of chitosan monomer. cDNA probes were synthesized from isolated RNA and labeled with fluorescent dye. They were hybridized with Human 3.8 II cDNA microarray, and the fluorescent signal was analyzed. cDNA microarray analysis revealed that 10 genes concerning to various signaling-related molecules were expressed at > = 2.0-fold higher signal ratio levels in the experimental group when compared with the control group after 3 days. Real-time PCR analysis showed that chitosan monomer induced an increase in the expression of four signal transduction genes, mitogen-activated protein ki-nase (MAPK)K3, MAPKKK11, Rac1 and Shc1, together with the alkaline phosphatase gene. These results suggest that a super-low concentration of chitosan monomer could modulate the activity of osteoblastic cells through mRNA levels and that chitosan monomer directly affects signal transduction inside cells.
机译:壳聚糖具有多种生物活性。尽管已经报道了壳聚糖促进骨损伤中的成骨作用,但是关于它如何在基因水平上调节硬组织形成细胞的知之甚少。这项研究的重点是用超低浓度的壳聚糖单体培养的成骨细胞中的基因表达。从分离的RNA合成cDNA探针,并用荧光染料标记。它们与人3.8 II cDNA微阵列杂交,并分析了荧光信号。 cDNA微阵列分析显示,与对照组相比,在3天后,与对照组相比,与各种信号相关分子有关的10个基因以> = 2.0倍的高信号比率水平表达。实时PCR分析表明,壳聚糖单体诱导了四个信号转导基因,有丝分裂原活化蛋白激酶(MAPK)K3,MAPKKK11,Rac1和Shc1,以及碱性磷酸酶基因的表达增加。这些结果表明,超低浓度的壳聚糖单体可以通过mRNA水平调节成骨细胞的活性,并且壳聚糖单体直接影响细胞内的信号转导。

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