Dahlin Rebecca L, Kinard Lucas A, Lam Johnny, Needham Clark J, Lu Steven, Kasper F Kurtis, Mikos Antonios G
Department of Bioengineering, Rice University, Houston, TX, USA.
Department of Bioengineering, Rice University, Houston, TX, USA.
Biomaterials. 2014 Aug;35(26):7460-9. doi: 10.1016/j.biomaterials.2014.05.055. Epub 2014 Jun 11.
This work investigated the ability of co-cultures of articular chondrocytes and mesenchymal stem cells (MSCs) to repair articular cartilage in osteochondral defects. Bovine articular chondrocytes and rat MSCs were seeded in isolation or in co-culture onto electrospun poly(ɛ-caprolactone) (PCL) scaffolds and implanted into an osteochondral defect in the trochlear groove of 12-week old Lewis rats. Additionally, a blank PCL scaffold and untreated defect were investigated. After 12 weeks, the extent of cartilage repair was analyzed through histological analysis, and the extent of bone healing was assessed by quantifying the total volume of mineralized bone in the defect through microcomputed tomography. Histological analysis revealed that the articular chondrocytes and co-cultures led to repair tissue that consisted of more hyaline-like cartilage tissue that was thicker and possessed more intense Safranin O staining. The MSC, blank PCL scaffold, and empty treatment groups generally led to the formation of fibrocartilage repair tissue. Microcomputed tomography revealed that while there was an equivalent amount of mineralized bone formation in the MSC, blank PCL, and empty treatment groups, the defects treated with chondrocytes or co-cultures had negligible mineralized bone formation. Overall, even with a reduced number of chondrocytes, co-cultures led to an equal level of cartilage repair compared to the chondrocyte samples, thus demonstrating the potential for the use of co-cultures of articular chondrocytes and MSCs for the in vivo repair of cartilage defects.
这项研究调查了关节软骨细胞与间充质干细胞(MSCs)共培养修复骨软骨缺损处关节软骨的能力。将牛关节软骨细胞和大鼠MSCs单独或共培养后接种到电纺聚己内酯(PCL)支架上,并植入12周龄Lewis大鼠滑车沟的骨软骨缺损处。此外,还研究了空白PCL支架和未处理的缺损情况。12周后,通过组织学分析评估软骨修复程度,通过微计算机断层扫描定量缺损处矿化骨的总体积来评估骨愈合程度。组织学分析显示,关节软骨细胞和共培养组形成的修复组织包含更多类似透明软骨的组织,更厚且番红O染色更强。MSC、空白PCL支架和空白处理组通常导致纤维软骨修复组织的形成。微计算机断层扫描显示,虽然MSC、空白PCL和空白处理组的矿化骨形成量相当,但软骨细胞或共培养组处理的缺损处矿化骨形成可忽略不计。总体而言,即使软骨细胞数量减少,与软骨细胞样本相比,共培养仍能实现同等程度的软骨修复,从而证明关节软骨细胞与MSCs共培养用于体内软骨缺损修复的潜力。