首页> 外文会议>Annual Meeting of the Japanese Association for Animal Cell Technology >DIFFERENT EXPRESSION OF GAP JUNCTIONAL PROTEIN CONNEXIN43 IN TWO STRAINS OF MICE AFTER ONE-MONTH IMPLANTATION OF POLY-L-LACTIC ACID
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DIFFERENT EXPRESSION OF GAP JUNCTIONAL PROTEIN CONNEXIN43 IN TWO STRAINS OF MICE AFTER ONE-MONTH IMPLANTATION OF POLY-L-LACTIC ACID

机译:聚-1乳酸单个月植入后两种小鼠两个菌株的间隙结蛋白Connexin43的不同表达

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The implantation of a biomaterial often induces host inflammatory responses. Some adverse effects by the biomaterials, such as poly-L-lactic acid (PLLA) and polyurethanes (PUs) were reported in animal experiments. PLLA produced tumorigenicity in ratsafter long-term implantation. The purpose of this study was to determine the in vitro effect of PLAO3 (high-molecular weights of PLLA) and PUS (PTMO/MDI/BD) on the function of the normal human dermal fibroblasts (NHDF) and the in vivo effect of PLAO3 onthe function of the cells originated from the subcutaneous tissue in the two female mouse strains, BALB/cJ and SJL/J. The results with Scrape-loading and dye transfer (SLOT) assay, Western Blot and RT-PCR analysis clearly demonstrated that gap-junctionalintercellular communication (GJIC) and the expression of Cx43 were significantly suppressed in PLAO3-implanted group of BALB/cJ mice in compared to the control mice. While, no significant difference was found in GJIC and the expression of mRNA level buta little bit difference was observed in the Cx43 protein expression between the SJL/J implanted and the control mice. We considered that the PLAO3 suppressed irreversibly gap junctional protein connexin43 at the earlier stage after implantation and thesuppression of connexin43 gene-expression might play a vital role in the inhibition of GJIC and thus promotes the tumorigenesis.
机译:生物材料的植入通常诱导宿主炎症反应。在动物实验中报道了生物材料的一些不良反应,例如聚-L-乳酸(PLLA)和聚氨酯(PU)。 PLLA在大鼠长期植入中产生致瘤性。本研究的目的是确定PlaO3(PLLA的高分子量)和PUS(PTMO / MDI / BD)对正常人体皮肤成纤维细胞(NHDF)的功能的体外效果和PLAO3的体内效应在两个雌性小鼠菌株中的皮下组织,BALB / CJ和SJL / J中的细胞功能源于皮下组织。刮刮加载和染料转移(槽)测定的结果,Western印迹和RT-PCR分析清楚地表明,在PlaO3植入的Balb / CJ小鼠中显着抑制了Gap-JunctionalIncercellulary通信(GJIC)和CX43的表达与对照小鼠相比。虽然,在GJIC中没有发现显着差异,并且在SJL / J植入和对照小鼠之间的CX43蛋白表达中观察到mRNA水平的表达。我们认为PlaO3在植入后抑制不可逆的间隙结蛋白Connexin43,并且Connexin43基因表达的ChexIn43基因表达的抑制可能在GJIC的抑制中发挥重要作用,从而促进肿瘤发生。

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