Bone Marrow Aspiration Concentrate and Platelet Rich Plasma for Osteochondral Repair in a Porcine Osteochondral Defect Model

被引:58
作者
Betsch, Marcel [1 ]
Schneppendahl, Johannes [1 ]
Thuns, Simon [1 ]
Herten, Monika [2 ]
Sager, Martin [3 ]
Jungbluth, Pascal [1 ]
Hakimi, Mohssen [1 ]
Wild, Michael [4 ]
机构
[1] Univ Hosp Duesseldorf, Dept Trauma & Hand Surg, Dusseldorf, Germany
[2] Univ Hosp Muenster, Clin Vasc & Endovasc Surg, Munster, Germany
[3] Univ Hosp Duesseldorf, Cent Anim Res Facil, Dusseldorf, Germany
[4] Klinikum Darmstadt, Dept Trauma & Orthopaed Surg, Darmstadt, Germany
关键词
MESENCHYMAL STEM-CELLS; AUTOLOGOUS CHONDROCYTE IMPLANTATION; BETA-TRICALCIUM PHOSPHATE; ARTICULAR-CARTILAGE; GROWTH-FACTOR; ANIMAL-MODELS; IN-VITRO; CLINICAL-USE; PROLIFERATION; REGENERATION;
D O I
10.1371/journal.pone.0071602
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Bone marrow aspiration concentrate (BMAC) may possess a high potency for cartilage and osseous defect healing because it contains stem cells and multiple growth factors. Alternatively, platelet rich plasma (PRP), which contains a cocktail of multiple growth factors released from enriched activated thrombocytes may potentially stimulate the mesenchymal stem cells (MSCs) in bone marrow to proliferate and differentiate. Methods: A critical size osteochondral defect (1066 mm) in both medial femoral condyles was created in 14 Goettinger mini-pigs. All animals were randomized into the following four groups: biphasic scaffold alone (TRUFIT BGS, Smith & Nephew, USA), scaffold with PRP, scaffold with BMAC and scaffold in combination with BMAC and PRP. After 26 weeks all animals were euthanized and histological slides were cut, stained and evaluated using a histological score and immunohistochemistry. Results: The thrombocyte number was significantly increased (p = 0.049) in PRP compared to whole blood. In addition the concentration of the measured growth factors in PRP such as BMP-2, BMP-7, VEGF, TGF-beta 1 and PDGF were significantly increased when compared to whole blood (p < 0.05). In the defects of the therapy groups areas of chondrogenic tissue were present, which stained blue with toluidine blue and positively for collagen type II. Adding BMAC or PRP in a biphasic scaffold led to a significant improvement of the histological score compared to the control group, but the combination of BMAC and PRP did not further enhance the histological score. Conclusions: The clinical application of BMAC or PRP in osteochondral defect healing is attractive because of their autologous origin and cost-effectiveness. Adding either PRP or BMAC to a biphasic scaffold led to a significantly better healing of osteochondral defects compared with the control group. However, the combination of both therapies did not further enhance healing.
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页数:12
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