Mishra Allan, Tummala Padmaja, King Aaron, Lee Byung, Kraus Mark, Tse Victor, Jacobs Christopher R
Menlo Sports Medicine, Menlo Park, California., USA.
Tissue Eng Part C Methods. 2009 Sep;15(3):431-5. doi: 10.1089/ten.tec.2008.0534.
The success of tissue engineering applications can potentially be dramatically improved with the addition of adjuncts that increase the proliferation and differentiation of progenitor or stem cells. Platelet-rich plasma (PRP) has recently emerged as a potential biologic tool to treat acute and chronic tendon disorders. The regenerative potential of PRP is based on the release of growth factors that occurs with platelet rupture. Its autologous nature gives it a significant advantage in tissue engineering applications. To test whether PRP may be useful specifically for cartilage regeneration, a cell culture experiment was devised in which mesenchymal stem cells (MSCs) were grown in control media or media enhanced with inactivated, buffered PRP. Proliferation 7 days after PRP treatment was increased: 1.041 versus 0.199 for the control media cells ( p<0.001). The messenger RNA (mRNA) level of the osteogenic marker RUNX2 was 52.84 versus 26.88 for the control group ( p<0.005). Likewise the mRNA level of the chondrogenic markers Sox-9 and aggrecan was 29.74 versus 2.29 for the control group ( p<0.001) and 21.04 versus 1.93 ( p<0.001), respectively. These results confirm that PRP enhances MSC proliferation and suggest that PRP causes chondrogenic differentiation of MSC in vitro.
通过添加能够促进祖细胞或干细胞增殖与分化的辅助剂,组织工程应用的成功率可能会得到显著提高。富血小板血浆(PRP)最近已成为治疗急慢性肌腱疾病的一种潜在生物工具。PRP的再生潜力基于血小板破裂时生长因子的释放。其自体性质使其在组织工程应用中具有显著优势。为了测试PRP是否特别有助于软骨再生,设计了一项细胞培养实验,其中间充质干细胞(MSCs)在对照培养基或添加了灭活缓冲PRP的培养基中培养。PRP处理7天后细胞增殖增加:对照培养基中的细胞为0.199,而PRP处理组为1.041(p<0.001)。成骨标志物RUNX2的信使核糖核酸(mRNA)水平在对照组为26.88,而在PRP处理组为52.84(p<0.005)。同样,软骨生成标志物Sox-9和聚集蛋白聚糖的mRNA水平在对照组分别为2.29和1.93,而在PRP处理组分别为29.74和(p<均0.001)。这些结果证实PRP可增强MSCs的增殖,并表明PRP可在体外诱导MSCs向软骨细胞分化。