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Preliminary experimental study of urethral reconstruction with tissue engineering and RNA interference techniques

机译:组织工程和RNA干扰技术对尿道重建的初步实验研究

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摘要

This study investigated the feasibility of replacing urinary epithelial cells with oral keratinocytes and transforming growth factor-β1(TGF-β1) small interfering RNA (siRNA)-transfected fibroblasts seeded on bladder acellular matrix graft (BAMG) in order to reconstruct tissue-engineered urethra.Constructed siRNAs,which expressed plasmids targeting TGF-β1,were transfected into rabbit fibroblasts.The effective siRNA was screened out by RT-PCR and was transfected into rabbit fibroblasts again.Synthesis of type Ⅰ collagen in culture medium was measured by enzyme-linked immuno sorbent assay (ELISA).Autologous oral keratinocytes and TGF-β1siRNA-transfected fibroblasts were seeded onto BAMGs to obtain a tissue-engineered mucosa.The tissue-engineered mucosa was assessed morphologically and with the help of scanning electron microscopy.The TGF-β1 siRNA decreased the expression of fibroblasts synthesis type Ⅰ collagen.Oral keratinocytes and TGF-β1 siRNA-transfected fibroblasts were seeded onto sterilized BAMG to obtain a tissue-engineered mucosa for urethral reconstruction.The compound graft was assessed using scanning electron microscope.Oral keratinocytes and TGF-β1 siRNA-transfected fibroblasts had a good compatibility with BAMG.The downregulation of fibroblasts synthesis type Ⅰ collagen expression by constructed siRNA interfering TGF-β1 provided a potential basis for genetic therapy of urethral scar.Oral keratinocytes and TGF-β 1 siRNA-transfected fibroblasts had good compatibility with BAMG and the compound graft could be a new choice for urethral reconstruction.
机译:本研究研究了用口服角蛋白细胞替代尿液上皮细胞和转化生长因子-β1(TGF-β1)小干扰RNA(siRNA) - 转染成纤维细胞的可行性,以进行膀胱细胞基质移植物(BAMG),以重建组织工程尿道表达靶向TGF-β1的质粒的末端siRNA被转染到兔成纤维细胞中。通过RT-PCR筛选出有效的siRNA,再次将培养基中Ⅰ型胶原蛋白转染到兔成纤维细胞中。通过酶联测量培养基中的Ⅰ型胶原蛋白的合成免疫吸附剂测定(ELISA)。将转发在BAMG上的异种口服角蛋白酶和TGF-β1SiRNA转染的成纤维细胞以获得组织工程化粘膜。在形态学上评估组织工程粘膜,并在扫描电子显微镜的帮助下进行评估。TGF-β1 siRNA降低了成纤维细胞合成Ⅰ型胶原蛋白的表达。将角蛋白细胞和TGF-β1SiRNA转染的成纤维细胞接种到S上Terilized BAMG以获得用于尿道重建的组织工程化粘膜。使用扫描电子显微镜评估复合接枝。静脉内细胞和TGF-β1siRNA转染的成纤维细胞与BAMG具有良好的相容性。成纤维细胞合成Ⅰ型胶原表达的下调构建的siRNA干扰TGF-β1为尿道瘢痕癌的遗传治疗提供了潜在的基础。角蛋白细胞和TGF-β1siRNA转染的成纤维细胞与BAMG具有良好的相容性,复合移植物可能是尿道重建的新选择。

著录项

  • 来源
    《亚洲男性学杂志(英文版)》 |2013年第3期|430-433|共4页
  • 作者

    Chao Li; Yue-Min Xu; Hong-Bin Li;

  • 作者单位

    Department of Urology, Sixth People's Hospital, Shanghai Jiaotong University, Shanghai 200233, China;

    Department of Urology, Sixth People's Hospital, Shanghai Jiaotong University, Shanghai 200233, China;

    Department of Urology, Sixth People's Hospital, Shanghai Jiaotong University, Shanghai 200233, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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