Chen Gang, Zheng Qian, Liu Mengfei, He Haiyang, Ju Xiaochen, Jiang Kan
Department of Joint Surgery, the Sixth Affiliated Hospital of Xinjiang Medical University, Urumqi Xinjiang, 830000, P. R. China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2023 Aug 15;37(8):1002-1010. doi: 10.7507/1002-1892.202305011.
To investigate the effect of Kartogenin (KGN) combined with adipose-derived stem cells (ADSCs) on tendon-bone healing after anterior cruciate ligament (ACL) reconstruction in rabbits.
After the primary ADSCs were cultured by passaging, the 3rd generation cells were cultured with 10 μmol/L KGN solution for 72 hours. The supernatant of KGN-ADSCs was harvested and mixed with fibrin glue at a ratio of 1∶1; the 3rd generation ADSCs were mixed with fibrin glue as a control. Eighty adult New Zealand white rabbits were taken and randomly divided into 4 groups: saline group (group A), ADSCs group (group B), KGN-ADSCs group (group C), and sham-operated group (group D). After the ACL reconstruction model was prepared in groups A-C, the saline, the mixture of ADSCs and fibrin glue, and the mixture of supernatant of KGN-ADSCs and fibrin glue were injected into the tendon-bone interface and tendon gap, respectively. ACL was only exposed without other treatment in group D. The general conditions of the animals were observed after operation. At 6 and 12 weeks, the tendon-bone interface tissues and ACL specimens were taken and the tendon-bone healing was observed by HE staining, c-Jun N-terminal kinase (JNK) immunohistochemical staining, and TUNEL apoptosis assay. The fibroblasts were counted, and the positive expression rate of JNK protein and apoptosis index (AI) were measured. At the same time point, the tensile strength test was performed to measure the maximum load and the maximum tensile distance to observe the biomechanical properties.
Twenty-eight rabbits were excluded from the study due to incision infection or death, and finally 12, 12, 12, and 16 rabbits in groups A-D were included in the study, respectively. After operation, the tendon-bone interface of groups A and B healed poorly, while group C healed well. At 6 and 12 weeks, the number of fibroblasts and positive expression rate of JNK protein in group C were significantly higher than those of groups A, B, and D (<0.05). Compared with 6 weeks, the number of fibroblasts gradually decreased and the positive expression rate of JNK protein and AI decreased in group C at 12 weeks after operation, with significant differences (<0.05). Biomechanical tests showed that the maximum loads at 6 and 12 weeks after operation in group C were higher than in groups A and B, but lower than those in group D, while the maximum tensile distance results were opposite, but the differences between groups were significant (<0.05).
After ACL reconstruction, local injection of a mixture of KGN-ADSCs and fibrin glue can promote the tendon-bone healing and enhance the mechanical strength and tensile resistance of the tendon-bone interface.
探讨软骨生成素(KGN)联合脂肪来源干细胞(ADSCs)对兔前交叉韧带(ACL)重建术后腱骨愈合的影响。
原代ADSCs传代培养后,将第3代细胞用10 μmol/L KGN溶液培养72小时。收集KGN-ADSCs的上清液并与纤维蛋白胶按1∶1的比例混合;将第3代ADSCs与纤维蛋白胶混合作为对照。取80只成年新西兰白兔,随机分为4组:生理盐水组(A组)、ADSCs组(B组)、KGN-ADSCs组(C组)和假手术组(D组)。在A-C组制备ACL重建模型后,分别将生理盐水、ADSCs与纤维蛋白胶的混合物、KGN-ADSCs的上清液与纤维蛋白胶的混合物注入腱骨界面和腱间隙。D组仅暴露ACL不做其他处理。术后观察动物的一般情况。在6周和12周时,取腱骨界面组织和ACL标本,通过苏木精-伊红(HE)染色、c-Jun氨基末端激酶(JNK)免疫组织化学染色和TUNEL凋亡检测观察腱骨愈合情况。计数成纤维细胞,测量JNK蛋白的阳性表达率和凋亡指数(AI)。在同一时间点进行拉伸强度测试,测量最大负荷和最大拉伸距离以观察生物力学性能。
因切口感染或死亡,28只兔子被排除在研究之外,最终A-D组分别有12、12、12和16只兔子纳入研究。术后,A组和B组的腱骨界面愈合较差,而C组愈合良好。在6周和12周时,C组的成纤维细胞数量和JNK蛋白阳性表达率显著高于A、B和D组(<0.05)。与6周时相比,C组术后12周时成纤维细胞数量逐渐减少,JNK蛋白阳性表达率和AI降低,差异有统计学意义(<0.05)。生物力学测试表明,C组术后6周和12周的最大负荷高于A组和B组,但低于D组,而最大拉伸距离结果相反,但组间差异有统计学意义(<0.05)。
ACL重建术后,局部注射KGN-ADSCs与纤维蛋白胶的混合物可促进腱骨愈合,增强腱骨界面的机械强度和抗拉伸能力。