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:富含血小板的血浆制备类型对人软骨下间充质祖细胞的软骨分化,迁移和增殖有影响

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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:通过蛋白聚糖和II型胶原的组织形态计量学评估,评估血小板浓缩液对人软骨下间充质祖细胞(MPC)的软骨形成潜力。此外,评估了血小板浓缩物的迁移和增殖作用。方法:使用制备试剂盒(自体条件血浆[ACP]试剂盒[Arthrex,那不勒斯,佛罗里达州]; Regen ACR-C试剂盒[Regen Lab,Le Mont-Sur-Lausanne,瑞士)制备富血小板血浆(PRP);以及PRP试剂盒(大韩民国首尔Rmedica)通过单采术(PRP-A)和离心(PRP-C)进行。与临床应用相反,随后进行冻融循环以激活血小板并防止体外残留纤维蛋白原引起的介质凝结。从股骨头的皮质海绵状骨中收获MPC。在高密度沉淀培养物中诱导MPC的软骨分化,并通过典型软骨基质成分的组织化学染色进行评估。使用趋化性分析评估MPC的迁移,并通过DNA含量测量增殖活性。结果:在5%ACP,Regen或Dr. PRP的情况下培养的MPC形成纤维组织,而在5%PRP-A或PRP-C刺激下的MPC则形成了致密而致密的软骨组织,富含II型胶原和蛋白聚糖。所有血小板均显着浓缩(ACP,P = .00041; Regen,P = .00029; Dr. PRP,P = .00051; PRP-A,P <.0001;和PRP-C,P <.0001)刺激了迁移。 MPC。除一个浓缩液(Dr. PRP,P = .63)外,所有血小板浓缩液均对MPC有增殖作用,如明显增加(ACP,P = .027;再生,P = .0029; PRP-A,P = .00021)所示。 ;以及PRP-C,P = .00069)的DNA含量。结论:通过不同制备方法获得的血小板浓缩物具有不同的刺激软骨分化,迁移和增殖的潜能。通过市售的制备试剂盒获得的浓缩血小板不能诱导MPC的软骨分化,而高度标准化的PRP制剂确实可以诱导这种分化。这些发现表明,基于干细胞的软骨修复中PRP治疗的结果不同。

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