Ge Dongxia, O'Brien Michael J, Savoie Felix H, Gimble Jeffrey M, Wu Xiying, Gilbert Margaret H, Clark-Patterson Gabrielle L, Schuster Jason D, Miller Kristin S, Wang Alun, Myers Leann, You Zongbing
Department of Structural and Cellular Biology, Tulane University School of Medicine, New Orleans, LA, USA.
Department of Orthopaedic Surgery, Tulane University School of Medicine, New Orleans, LA, USA.
NPJ Regen Med. 2021 Nov 30;6(1):82. doi: 10.1038/s41536-021-00192-6.
Localized cartilage lesions in early osteoarthritis and acute joint injuries are usually treated surgically to restore function and relieve pain. However, a persistent clinical challenge remains in how to repair the cartilage lesions. We expressed doublecortin (DCX) in human adipose-derived stromal/stem cells (hASCs) and engineered hASCs into cartilage tissues using an in vitro 96-well pellet culture system. The cartilage tissue constructs with and without DCX expression were implanted in the knee cartilage defects of rabbits (n = 42) and monkeys (n = 12). Cohorts of animals were euthanized at 6, 12, and 24 months after surgery to evaluate the cartilage repair outcomes. We found that DCX expression in hASCs increased expression of growth differentiation factor 5 (GDF5) and matrilin 2 in the engineered cartilage tissues. The cartilage tissues with DCX expression significantly enhanced cartilage repair as assessed macroscopically and histologically at 6, 12, and 24 months after implantation in the rabbits and 24 months after implantation in the monkeys, compared to the cartilage tissues without DCX expression. These findings suggest that hASCs expressing DCX may be engineered into cartilage tissues that can be used to treat localized cartilage lesions.
早期骨关节炎和急性关节损伤中的局部软骨损伤通常通过手术治疗以恢复功能和缓解疼痛。然而,在如何修复软骨损伤方面仍然存在持续的临床挑战。我们在人脂肪来源的基质/干细胞(hASC)中表达双皮质素(DCX),并使用体外96孔微团培养系统将hASC工程化为软骨组织。将表达和不表达DCX的软骨组织构建体植入兔(n = 42)和猴(n = 12)的膝关节软骨缺损处。在手术后6、12和24个月对动物进行安乐死,以评估软骨修复结果。我们发现hASC中DCX的表达增加了工程化软骨组织中生长分化因子5(GDF5)和Ⅱ型胶原微原纤维蛋白(matrilin 2)的表达。与不表达DCX的软骨组织相比,在兔植入后6、12和24个月以及猴植入后24个月,通过宏观和组织学评估,表达DCX的软骨组织显著增强了软骨修复。这些发现表明,表达DCX的hASC可以被工程化为可用于治疗局部软骨损伤的软骨组织。