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The effects of platelet releasate on the migration and proliferation of bone marrow-derived cells cultured under osteogenic conditions.

机译:血小板释放物对成骨条件下培养的骨髓源细胞迁移和增殖的影响。

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Concentrated platelets and their products are currently being used as a clinical tool to accelerate endosseous wound healing. However, there is a lack of understanding regarding the actions of platelets and platelet released products on osteogenic cells. In the current study, we show that releasate from thrombin activated platelets increases the migration and proliferation of osteogenic cultures of bone marrow cells by a dose-dependent mechanism. Using a scratch wound assay, we demonstrated that platelet releasate (PR) stimulated up to a 2.40 +/- 0.50-fold increase in scratch closure in serum-free medium, relative to a control containing thrombin. In the presence of serum, the addition of PR resulted in a 1.45 +/- 0.13-fold increase in scratch closure. To isolate migration from proliferation, cell monolayers were pre-incubated with 5, 10 and 20 mug/ml of Mitomycin C (MMC), which inhibits cell division. This resulted in a large overall decrease in the leading front of scratch closure, which indicated that PR stimulated cell mitogenesis. However, irrespective of MMC pre-treatment, PR stimulated a motogenic response. These results provide a possible mechanism whereby platelets may influence bone regeneration.
机译:浓缩血小板及其产物目前被用作加速骨内伤口愈合的临床工具。然而,对于血小板和血小板释放产物对成骨细胞的作用缺乏了解。在当前的研究中,我们显示凝血酶活化的血小板释放物通过剂量依赖性机制增加了骨髓细胞成骨培养物的迁移和增殖。使用刮擦伤口试验,我们证明了相对于含有凝血酶的对照,血小板释放液(PR)在无血清培养基中刺激的刮擦闭合提高了2.40 +/- 0.50倍。在存在血清的情况下,PR的添加导致划痕闭合增加1.45 +/- 0.13倍。为了从迁移中分离迁移,将细胞单层与抑制细胞分裂的5、10和20杯/毫升丝裂霉素C(MMC)预孵育。这导致划痕闭合的前缘总体上总体下降,这表明PR刺激了细胞有丝分裂。然而,不管MMC预处理如何,PR均刺激了致机体反应。这些结果提供了可能的机制,其中血小板可能影响骨骼再生。

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