Birdwhistell Kate E, Karumbaiah Lohitash, Franklin Samuel P
Department of Small Animal Medicine and Surgery, Veterinary Teaching Hospital, University of Georgia, Athens, Georgia.
Department of Regenerative Medicine, Edgar L. Rhodes Center for Animal and Dairy Sciences, University of Georgia, Athens, Georgia.
J Knee Surg. 2018 May;31(5):410-415. doi: 10.1055/s-0037-1603801. Epub 2017 Jun 23.
Activated platelet-rich plasma (PRP), also referred to as platelet-rich fibrin (PRF), has been used to augment numerous techniques of cartilage repair in the knee but does not always result in superior quality of repair tissue. One possible reason that PRF does not consistently result in excellent cartilage regeneration is the transiency of growth factor provision with PRF. The objective of this study was to compare the release of transforming growth factor (TGF)-β1 from PRF and from PRP combined with a novel chondroitin sulfate glycosaminoglycan (CS-GAG) gel. PRP was prepared from nine healthy dogs and split into two aliquots: one activated with bovine thrombin and calcium chloride (CaCl) to form PRF and the other aliquot was used to rehydrate a lyophilized CS-GAG gel. Both PRF and the CS-GAG gels were incubated in media for 13 days and media were collected, stored, and replaced every 48 hours and the concentration of TGF-β1 quantified in the media using an enzyme-linked immunosorbent assay. Concentrations of TGF-β1 in the media were up to three times greater with the CS-GAG gels and were significantly ( < 0.05) greater than with PRF on days 3, 5, 7, 9, and 13. Furthermore, TGF-β1 elution was still substantial at day 13 with the use of the CS-GAG gels. Additional in vitro work is warranted to characterize TGF-β1 elution from this CS-GAG gel with human PRP and to determine whether the use of these CS-GAG gels can augment cartilage repair in vivo.
活化富血小板血浆(PRP),也被称为富血小板纤维蛋白(PRF),已被用于增强膝关节软骨修复的多种技术,但并不总是能产生质量更优的修复组织。PRF不能始终如一地产生出色软骨再生的一个可能原因是PRF提供生长因子的短暂性。本研究的目的是比较PRF和PRP与一种新型硫酸软骨素糖胺聚糖(CS-GAG)凝胶联合使用时转化生长因子(TGF)-β1的释放情况。从九只健康犬制备PRP,并分成两份:一份用牛凝血酶和氯化钙(CaCl)激活形成PRF,另一份用于复水冻干的CS-GAG凝胶。将PRF和CS-GAG凝胶在培养基中孵育13天,每48小时收集、储存并更换培养基,使用酶联免疫吸附测定法对培养基中TGF-β1的浓度进行定量。CS-GAG凝胶培养基中TGF-β1的浓度高达PRF的三倍,并且在第3、5、7、9和13天显著(<0.05)高于PRF。此外,使用CS-GAG凝胶在第13天时TGF-β1的洗脱量仍然很大。有必要进行额外的体外研究,以表征这种CS-GAG凝胶与人类PRP一起时TGF-β1的洗脱情况,并确定使用这些CS-GAG凝胶是否能增强体内软骨修复。