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首页> 外文期刊>Arthroscopy: the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association >Platelet-Rich Plasma Preparation Types Show Impact on Chondrogenic Differentiation, Migration, and Proliferation of Human Subchondral Mesenchymal Progenitor Cells
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Platelet-Rich Plasma Preparation Types Show Impact on Chondrogenic Differentiation, Migration, and Proliferation of Human Subchondral Mesenchymal Progenitor Cells

机译:富含血小板血浆制备类型节目的影响在Chondrogenic分化、迁移和人类软骨下间叶细胞的增殖祖细胞

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Purpose: To evaluate the chondrogenic potential of platelet concentrates on human subchondral mesenchymal progenitor cells (MPCs) as assessed by histomorphometric analysis of proteoglycans and type II collagen. Furthermore, the migratory and proliferative effect of platelet concentrates were assessed. Methods: Platelet-rich plasma (PRP) was prepared using preparation kits (Autologous Conditioned Plasma [ACP] Kit [Arthrex, Naples, FL]; Regen ACR-C Kit [Regen Lab, Le Mont-Sur-Lausanne, Switzerland]; and Dr. PRP Kit [Rmedica, Seoul, Republic of Korea]) by apheresis (PRP-A) and by centrifugation (PRP-C). In contrast to clinical application, freeze-and-thaw cycles were subsequently performed to activate platelets and to prevent medium coagulation by residual fibrinogen in vitro. MPCs were harvested from the cortico-spongious bone of femoral heads. Chondrogenic differentiation of MPCs was induced in high-density pellet cultures and evaluated by histochemical staining of typical cartilage matrix components. Migration of MPCs was assessed using a chemotaxis assay, and proliferation activity was measured by DNA content. Results: MPCs cultured in the presence of 5% ACP, Regen, or Dr. PRP formed fibrous tissue, whereas MPCs stimulated with 5% PRP-A or PRP-C developed compact and dense cartilaginous tissue rich in type II collagen and proteoglycans. All platelet concentrates significantly (ACP, P = .00041; Regen, P = .00029; Dr. PRP, P = .00051; PRP-A, P < .0001; and PRP-C, P < .0001) stimulated migration of MPCs. All platelet concentrates but one (Dr. PRP, P = .63) showed a proliferative effect on MPCs, as shown by significant increases (ACP, P = .027; Regen, P = .0029; PRP-A, P = .00021; and PRP-C, P = .00069) in DNA content. Conclusions: Platelet concentrates obtained by different preparation methods exhibit different potentials to stimulate chondrogenic differentiation, migration, and proliferation of MPCs. Platelet concentrates obtained by commercially available preparation kits failed to induce chondrogenic differentiation of MPCs, whereas highly standardized PRP preparations did induce such differentiation. These findings suggest differing outcomes with PRP treatment in stem cellebased cartilage repair.
机译:目的:评估的chondrogenic潜力血小板集中于人类软骨下间叶细胞祖细胞(mpc)评估蛋白聚糖的histomorphometric分析和II型胶原蛋白。和增殖的影响血小板浓缩液被评估。(PRP)准备使用准备工具(自体的等离子体(ACP)工具包[Arthrex那不勒斯,FL];PRP套件[Rmedica,首尔,韩国])apheresis (PRP-A)和离心(PRP-C)。与临床应用相比,随后freeze-and-thaw周期激活血小板,并防止执行残留的纤维蛋白原培养基凝固体外。cortico-spongious骨股头。Chondrogenic mpc的分化诱导在高密度颗粒文化和评估组织化学染色典型的软骨矩阵的组件。使用趋化性试验和增殖活动是由DNA测量内容。mpc的机场核心计划的5%,回复,或博士PRP形成纤维组织,而mpc刺激与5% PRP-A或PRP-C发达紧凑而丰富的致密的软骨组织II型胶原和蛋白聚糖。集中显著(P = .00041机场核心计划;回复,P = .00029;<。;mpc的迁移。PRP博士(P =点)显示增殖影响mpc,见显著增加(ACP, P = .027;.00021;结论:血小板浓缩获得的不同的制备方法势来刺激chondrogenic分化、迁移和扩散货币政策委员会。商用设备未能做准备诱导chondrogenic mpc的分化,而高度标准化PRP制剂诱导分化。建议与PRP治疗不同的结果茎cellebased软骨修复。

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