...
首页> 外文期刊>Tissue engineering >The regenerative effects of platelet-rich plasma on meniscal cells in vitro and its in vivo application with biodegradable gelatin hydrogel.
【24h】

The regenerative effects of platelet-rich plasma on meniscal cells in vitro and its in vivo application with biodegradable gelatin hydrogel.

机译:富血小板血浆对半月板细胞的再生作用及其可生物降解的明胶水凝胶的体内应用。

获取原文
获取原文并翻译 | 示例
           

摘要

The objective of the study was to test the hypothesis that platelet-rich plasma (PRP) enhances meniscal tissue regeneration in vitro and in vivo. In the in vitro study, monolayer meniscal cell cultures were prepared, and 3-(4,5-dimethylthiazol-2yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2 H-tetrazolium inner salt assay and 5-bromo-2'-deoxyuridine assay were performed to assess proliferative behavior in the presence of PRP. Alcian blue assay was performed to assess extracellular matrix (ECM) synthesis. To detect the fibrocartilage-related messenger ribonucleic acid (mRNA) expressions, real-time polymerase chain reaction was performed. In the in vivo study, 1.5-mm-diameter full-thickness defects were created in the avascular region of rabbit meniscus. Gelatin hydrogel (GH) was used as the drug delivery system for PRP growth factors. The defects were filled as follows: Group A, GH with PRP; Group B, GH with platelet-poor plasma; Group C, GH only. Each group was evaluated histologically at 4, 8, and 12 weeks after surgery. PRP stimulated deoxyribonucleic acid synthesis and ECM synthesis (p<0.05). Meniscal cells cultured with PRP showed greater mRNA expression of biglycan and decorin (p<0.05). Histological findings showed that remnants of gelatin hydrogels existed at 4 weeks, indicating that the hydrogels could control release for approximately 4 weeks. Histological scoring of the defect sites at 12 weeks revealed significantly better meniscal repair in animals that received PRP with GH than in the other two groups. These findings suggest that PRP enhances the healing of meniscal defects.
机译:该研究的目的是检验以下假设:富含血小板的血浆(PRP)在体外和体内可增强半月板组织的再生。在体外研究中,制备了单层半月板细胞培养物,并进行了3-(4,5-二甲基噻唑-2-基)-5-(3-羧基甲氧基苯基)-2-(4-磺基苯基)-2 H-四唑内盐的测定和进行5-溴-2'-脱氧尿苷测定以评估在PRP存在下的增殖行为。进行了阿尔辛蓝测定以评估细胞外基质(ECM)的合成。为了检测与纤维软骨相关的信使核糖核酸(mRNA)的表达,进行了实时聚合酶链反应。在体内研究中,在兔半月板的无血管区域中产生了1.5毫米直径的全厚度缺陷。明胶水凝胶(GH)用作PRP生长因子的药物递送系统。缺陷填充如下:A组,GH伴PRP; B组,血浆贫血的GH; C组,仅限GH。在手术后第4、8和12周对每组进行组织学评估。 PRP刺激了脱氧核糖核酸的合成和ECM的合成(p <0.05)。用PRP培养的半月板细胞显示Biglycan和Decorin的mRNA表达更高(p <0.05)。组织学发现表明,明胶水凝胶在4周时残留,表明该水凝胶可以控制释放约4周。组织缺损部位在12周时的组织学评分显示,接受GH的PRP的动物的半月板修复明显好于其他两组。这些发现表明,PRP增强了半月板缺损的愈合。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号