Cenni E, Ciapetti G, Pagani S, Perut F, Giunti A, Baldini N
Laboratory for Pathophysiology of Orthopedic Implants, Rizzoli Orthopedic Institute, Bologna, Italy.
J Periodontol. 2005 Mar;76(3):323-8. doi: 10.1902/jop.2005.76.3.323.
Platelet alpha granules contain growth factors released into the surrounding environment during activation. This property has been used in clinical medicine to accelerate the repair process by activating in vitro autologous platelets with thrombin and has also been proposed to promote the proliferation of bone cells. The aim of this research was to assess the effect of platelet concentrates activated with thrombin on human gingival fibroblasts and human osteoblasts from trabecular bone.
Platelet concentrates, activated with bovine thrombin, were added to the cells in serum-free medium. The cultures were assessed for proliferation by vital stain and cell count after 72-hour incubation. Alkaline phosphatase activity was tested after 72-hour incubation on the osteoblast lysates by a colorimetric assay. After 21 days the formation of mineral nodules was tested in the osteoblast cultures by alizarin red staining. The effects of the activated platelet concentrates (APC) were compared with the serum-free medium (SF), or with platelet-poor plasma added medium (PPP).
The fibroblast growth in the presence of APC was higher, though not significantly, than SF. APC resulted in a nonsignificant decrease in proliferation and alkaline phosphatase expression in osteoblasts, compared both to serum free medium, and PPP. Mineralization was only modestly increased after incubation with APC in comparison with serum-free medium.
There were no statistical differences in fibroblast proliferation, or in osteoblast growth and functions between serum-free conditions and the platelet gel treatment. Therefore, neither fibroblast proliferation nor osteoblast growth and functions were affected by the activated platelet concentrates in vitro.
血小板α颗粒含有在激活过程中释放到周围环境中的生长因子。这一特性已在临床医学中用于通过用凝血酶激活体外自体血小板来加速修复过程,并且也有人提出其可促进骨细胞增殖。本研究的目的是评估经凝血酶激活的血小板浓缩物对人牙龈成纤维细胞和来自松质骨的人成骨细胞的影响。
将用牛凝血酶激活的血小板浓缩物添加到无血清培养基中的细胞中。培养72小时后,通过活细胞染色和细胞计数评估细胞增殖情况。通过比色法在成骨细胞裂解物中培养72小时后检测碱性磷酸酶活性。21天后,通过茜素红染色检测成骨细胞培养物中矿化结节的形成。将激活的血小板浓缩物(APC)的作用与无血清培养基(SF)或添加了贫血小板血浆的培养基(PPP)进行比较。
在APC存在下,成纤维细胞的生长高于SF,但差异不显著。与无血清培养基和PPP相比,APC导致成骨细胞的增殖和碱性磷酸酶表达无显著降低。与无血清培养基相比,与APC孵育后矿化仅适度增加。
在无血清条件和血小板凝胶处理之间,成纤维细胞增殖、成骨细胞生长和功能方面没有统计学差异。因此,激活的血小板浓缩物在体外对成纤维细胞增殖、成骨细胞生长和功能均无影响。