Division of Orthopaedic Surgery, McGill University, Montreal, Quebec, Canada H3H 2P2.
J Tissue Eng. 2011;2011:587547. doi: 10.4061/2011/587547. Epub 2011 Jul 25.
The expression of type X collagen (COL X), a late-stage chondrocyte hypertrophy marker in human mesenchymal stem cells (MSCs) from osteoarthritis (OA) patients poses a major setback to current cartilage and intervertebral disc tissue engineering efforts. However, it is not yet clear whether COL X is expressed by all human bone marrow stem cells or if it is related to age, gender, site, disease status, or drug therapy. In the current study, we report that COL X expression is upregulated in MSCs from rabbits in a surgical instability model of OA (anterior cruciate ligament transection (ACLT)) when compared to control rabbit MSCs. Thus COL X expression in OA is a common phenomenon that is due to the disease process itself and not to other environmental factors. It is, therefore, critical to understand MSC phenotype in OA patients, as these cells are essential clinically for biological repair of cartilage lesions using autologous stem cells.
型胶原(COL X)的表达是人类骨关节炎(OA)患者间充质干细胞(MSC)晚期软骨细胞肥大的标志物,这对当前软骨和椎间盘组织工程的努力构成了重大挑战。然而,目前尚不清楚 COL X 是否由所有人类骨髓干细胞表达,或者它是否与年龄、性别、部位、疾病状态或药物治疗有关。在本研究中,我们报告称,与对照兔 MSC 相比,OA 手术不稳定模型(前交叉韧带切断术(ACLT))中的兔 MSC 中 COL X 的表达上调。因此,OA 中的 COL X 表达是一种普遍现象,是由疾病过程本身引起的,而不是其他环境因素引起的。因此,了解 OA 患者 MSC 的表型至关重要,因为这些细胞对于使用自体干细胞进行软骨损伤的生物修复具有重要的临床意义。