Liu Qi, Victor Marino, Mark Bartold
Dept. of Periodontology, Dental Hospital of Zunyi Medical College, Zunyi 563003, China.
Hua Xi Kou Qiang Yi Xue Za Zhi. 2006 Feb;24(1):15-7, 35.
To investigate the development of novel cell delivery carriers and evaluate the effects of platelet-rich plasma (PRP) and platelet-poor plasma (PPP) on cellular attachment and proliferation.
Rat gingival fibroblasts, periodontal ligament fibroblasts and osteoblasts were cultured in vitro. The biodegradable membranes were treated with PRP and PPP that were obtained from rat whole blood by gradient density centrifugation. The cellular attachment, proliferation and morphology on the untreated membranes and membranes treated with PRP and PPP were tested in vitro for 48 hours.
There were significant differences between the untreated membranes and the membranes treated with PRP and PPP for three kinds of rat cells used in the experiment. There were no significant differences between those membranes treated with PRP and those treated with PPP. Three kinds of cells on the membranes treated with PRP were slight higher than those on the membranes treated with PPP. There were no significant differences in the same group for cells attachment. The rate of different cells proliferation on the untreated membranes was significant lower than those on the membranes treated with PRP and PPP at 1 hour and 48 hours after seeding. At the same time, the rate of different cells proliferation on the treated membranes at 48 hours was significant higher than those on the treated membranes at 1 hour. There was no significant differences in the same group for the rate of cells proliferation. Most of the cells attached on the membranes treated with PRP and PPP exhibited robust and elongated forms with numerous filopodial extensions.
The results showed that the biodegradable membranes treated with PRP and PPP could promote rat cell attachment and proliferation. It suggests that this novel technique will provide the experimental basis for the development of cell delivery carriers and periodontal regeneration.
研究新型细胞递送载体的开发,并评估富血小板血浆(PRP)和贫血小板血浆(PPP)对细胞黏附和增殖的影响。
体外培养大鼠牙龈成纤维细胞、牙周膜成纤维细胞和成骨细胞。通过梯度密度离心从大鼠全血中获得的PRP和PPP处理可生物降解膜。在体外对未处理的膜以及用PRP和PPP处理的膜上的细胞黏附、增殖和形态进行48小时测试。
实验中使用的三种大鼠细胞在未处理的膜与用PRP和PPP处理的膜之间存在显著差异。用PRP处理的膜与用PPP处理的膜之间无显著差异。用PRP处理的膜上的三种细胞略高于用PPP处理的膜上的细胞。同一组内细胞黏附无显著差异。接种后1小时和48小时,未处理膜上不同细胞的增殖率显著低于用PRP和PPP处理的膜上的增殖率。同时,处理后膜上48小时不同细胞的增殖率显著高于1小时时的增殖率。同一组内细胞增殖率无显著差异。大多数附着在用PRP和PPP处理的膜上的细胞呈现出粗壮且伸长的形态,有许多丝状伪足延伸。
结果表明,用PRP和PPP处理的可生物降解膜可促进大鼠细胞的黏附和增殖。这表明这项新技术将为细胞递送载体的开发和牙周再生提供实验依据。