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Effect of Collagen -Activated Platelet-Rich Plasma to Synthesis of Extracellular Matrix in Fibroblast of Periodontal Ligament

机译:胶原致动血小板血浆对牙周韧带成纤维细胞胞外基质合成的影响

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The aim of this study was to investigate the activation effect of PRP using collagen to the synthesis of extracellular matrix in fibroblasts of the periodontal ligament. The PRP from the human donor was activated using collagen (collagen-activated PRP) and compared with inactivated PRP as a control group. The groups have measured the deposit of extracellular matrix during the three and seven days for observation. The collagen-activated PRP resulted in a more significant release of extracellular matrix compared with control group. And, there were substantial differences of extracellular matrix deposit in the three and seven days for observation. We obtained that the use of collagen on PRP as an alternative to stimulate platelet-associated growth factors and give greater extracellular matrix synthesis. The polypeptide growth factor (PGFs) is a biological mediator in periodontal regeneration. These materials are desirable because of regulatory effects on proliferation and differentiation of bone cells and connective tissues. Platelet Derived Growth Factor (PDGF) and Transforming Growth Factor - β (TGF - β) are the most potent stimulators of PGFs for fibroblasts in cell migration, and proliferation as well as in the synthesis of extracellular matrix. It is vital in the process of wound healing. Platelet - Rich Plasma could improve the activity of extracellular matrix synthesis of periodontal ligament fibroblasts. The addition of rat tail collagen in PRP did not affect the increase in extracellular matrix synthesis activity of periodontal ligament fibroblasts. Addition collacure collagen sponge on the PRP was affected on the growing movement of the extracellular matrix of periodontal ligament fibroblasts.
机译:本研究的目的是研究PRP使用胶原蛋白对牙周韧带成纤维细胞的合成的活化作用。使用胶原蛋白(胶原活化的PRP)活化来自人类供体的PRP,并与灭活的PRP作为对照组进行比较。该组在三个和七天内测量了细胞外基质的沉积以进行观察。与对照组相比,胶原活化的PRP导致细胞外基质的释放更大。并且,在三天和七天内具有显着差异进行观察。我们获得了在PRP上使用胶原蛋白作为刺激血小板相关生长因子的替代方案,并提供更大的细胞外基质合成。多肽生长因子(PGF)是牙周再生中的生物介体。由于对骨细胞和结缔组织的增殖和分化的调节作用,这些材料是理想的。血小板衍生的生长因子(PDGF)和转化生长因子 - β(TGF - β)是细胞迁移中的成纤维细胞的PGFS最有效的刺激器,以及细胞外基质的合成。在伤口愈合过程中至关重要。富含血小板的血浆可以改善细胞外韧带成纤维细胞的细胞外基质合成的活性。在PRP中添加大鼠尾胶原蛋白并未影响牙周韧带成纤维细胞的细胞外基质合成活性的增加。 PRP上的加成凝聚胶原蛋白海绵受到牙周韧带成纤维细胞细胞外基质的越来越多的运动。

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