Tissue Engineering Centre, Universiti Kebangsaan Malaysia Medical Centre, Jalan Yaacob Latif, Bandar Tun Razak, Cheras 56000, K.L, Malaysia; Bioartificial Organ and Regenerative Medicine Unit, National Defence University of Malaysia, Sungai Besi Camp 57000, K.L, Malaysia.
Tissue Engineering Centre, Universiti Kebangsaan Malaysia Medical Centre, Jalan Yaacob Latif, Bandar Tun Razak, Cheras 56000, K.L, Malaysia.
Exp Gerontol. 2018 Apr;104:43-51. doi: 10.1016/j.exger.2018.01.020. Epub 2018 Feb 3.
Hyaline articular cartilage, which protects the bones of diarthrodial joints from forces associated with load bearing, frictions, and impacts has very limited capacities for self-repair. Over the years, the trend of treatments has shifted to regenerations and researchers have been on the quest for a lasting regeneration. We evaluated the treatment of osteoarthritis by chondrogenically induced ADSCs and BMSCs for a long time functional recovery.
Osteoarthritis was induced at the right knee of sheep by complete resection of ACL and medial meniscus. Stem cells from sheep were induced to chondrogenic lineage. Test sheep received 5 mls single doses of 2 × 10 autologous PKH26-labelled ADSCs or BMSCs, while controls received basal medium. Functional recovery of the knees was evaluated via electromyography.
Induced ADSCs had 625, 255, 393, 908, 409, 157 and 1062 folds increases of collagen I, collagen II, aggrecan, SOX9, cartilage oligomeric protein, chondroadherin and fibromodullin compare to uninduced cells, while BMSCs had 702, 657, 321, 276, 337, 233 and 1163 respectively; p = .001. Immunocytochemistry was positive for these chondrogenic markers. 12 months post-treatment, controls scored 4 in most regions using ICRS, while the treated had 8; P = .001. Regenerated cartilages were positive to PKH26 and demonstrated the presence of condensing cartilages on haematoxylin and eosin; and Safranin O. OA degenerations caused significant amplitude shift from right to left hind limb. After treatments, controls persisted with significant decreases; while treated samples regained balance.
Both ADSCs and BMSCs had increased chondrogenic gene expressions using TGF-β3 and BMP-6. The treated knees had improved cartilage scores; PKH26 can provide elongated tracking, while EMG results revealed improved joint recoveries. These could be suitable therapies for osteoarthritis.
透明软骨覆盖于关节表面,保护关节免受负重、摩擦和冲击等力学因素的损伤,但透明软骨自我修复的能力非常有限。多年来,治疗方法的趋势已经转向再生,研究人员一直在寻找一种持久的再生方法。我们评估了软骨诱导的 ADSC 和 BMSC 治疗骨关节炎以实现长期功能恢复的效果。
通过完全切除 ACL 和内侧半月板在绵羊的右膝关节诱导骨关节炎。将绵羊的干细胞诱导为软骨谱系。实验组绵羊接受 5ml 单次剂量的 2×10 个自体 PKH26 标记的 ADSC 或 BMSC,对照组接受基础培养基。通过肌电图评估膝关节的功能恢复情况。
与未诱导的细胞相比,诱导的 ADSC 中胶原蛋白 I、胶原蛋白 II、聚集蛋白聚糖、SOX9、软骨寡聚蛋白、软骨粘连蛋白和纤维调节素分别增加了 625、255、393、908、409、157 和 1062 倍,BMSC 分别增加了 702、657、321、276、337、233 和 1163 倍;p=0.001。免疫细胞化学染色这些软骨形成标志物呈阳性。治疗 12 个月后,对照组 ICRS 评分大部分区域为 4 分,而治疗组为 8 分;p=0.001。再生软骨对 PKH26 呈阳性,并在苏木精和伊红染色以及番红 O 染色中显示出浓缩软骨的存在。OA 退变导致右侧和左侧后肢的振幅显著偏移。治疗后,对照组的振幅持续显著下降,而治疗组的振幅恢复平衡。
TGF-β3 和 BMP-6 均能增加 ADSC 和 BMSC 的软骨形成基因表达。治疗后的膝关节软骨评分得到改善;PKH26 可提供更长的追踪效果,而肌电图结果显示关节恢复情况得到改善。这些方法可能适用于骨关节炎的治疗。