Slapnicka Jan, Fassmann Antonin, Strasak Ludek, Augustin Peter, Vanek Jiri
Department of Oral and Maxillofacial Surgery, University Hospital Brno Bohunice, Dental Research Center, Masaryk University, Brno, Czech Republic.
J Oral Maxillofac Surg. 2008 Feb;66(2):297-301. doi: 10.1016/j.joms.2007.05.022.
The purpose of this study was to evaluate the effect of progressively increasing concentrations of activated and nonactivated platelet-rich plasma (PRP) on proliferation of human osteoblasts in vitro.
Human osteoblasts (hFOB 1.19) obtained from the American Type Culture Collection (ATCC, Manassas, VA) were used in the experiment. PRP was obtained from a 28-year-old healthy male volunteer by means of a Haemonetics gradient density cell separator (Haemonetics, Munich, Germany). Human thrombin was used to activate PRP. Three independent experiments were conducted. Samples containing 10% (0.38x increase in platelet count), 25% (0.95x increase in platelet count), 50% (1.95x increase in platelet count), and 75% (2.86x increase in platelet count) of activated PRP and nonactivated PRP were prepared including controls. After culture periods of 24, 48, and 72 hours osteoblast proliferation was evaluated by counting the number of cells using a Multisizer 3 Coulter Counter (Beckman Coulter, Inc, Fullerton, CA).
After 24, 48, and 72 hours of incubation, the number of cells in the control group (without PRP) was higher than that of cells in samples containing activated or nonactivated PRP. Osteoblasts with 10% activated PRP (0.38x increase in platelet count) had the highest viability of all samples containing PRP.
Activated PRP resulted in higher proliferation of osteoblasts compared with nonactivated PRP at concentrations of 10% (0.38x increase in platelet count) and 25% (0.95x increase in platelet count) in culture. This study failed to show significant increases in proliferation of human osteoblasts treated with activated or nonactivated PRP compared with controls in vitro.
本研究旨在评估逐步增加浓度的活化和未活化富血小板血浆(PRP)对人成骨细胞体外增殖的影响。
实验采用从美国典型培养物保藏中心(ATCC,弗吉尼亚州马纳萨斯)获取的人成骨细胞(hFOB 1.19)。PRP通过海莫奈蒂克斯梯度密度细胞分离器(海莫奈蒂克斯,德国慕尼黑)从一名28岁健康男性志愿者体内获取。用人凝血酶激活PRP。进行了三项独立实验。制备了含10%(血小板计数增加0.38倍)、25%(血小板计数增加0.95倍)、50%(血小板计数增加1.95倍)和75%(血小板计数增加2.86倍)活化PRP和未活化PRP的样本,包括对照组。在培养24、48和72小时后,使用Multisizer 3库尔特计数器(贝克曼库尔特公司,加利福尼亚州富勒顿)通过计数细胞数量来评估成骨细胞增殖情况。
孵育24、48和72小时后,对照组(无PRP)中的细胞数量高于含活化或未活化PRP样本中的细胞数量。含10%活化PRP(血小板计数增加0.38倍)的成骨细胞在所有含PRP的样本中活力最高。
在培养中,与未活化PRP相比,浓度为10%(血小板计数增加0.38倍)和25%(血小板计数增加0.95倍)的活化PRP可导致成骨细胞更高的增殖。本研究未能显示与对照组相比,体外经活化或未活化PRP处理的人成骨细胞增殖有显著增加。