Department of Veterinary Science, University of Kentucky, Lexington, KY 40546, USA.
Osteoarthritis Cartilage. 2012 Nov;20(11):1347-56. doi: 10.1016/j.joca.2012.07.002. Epub 2012 Jul 16.
Knowledge of mechanisms directing diarthrodial joint development may be useful in understanding joint pathologies and identifying new therapies. We have previously established that axolotl salamanders can fully repair large articular cartilage lesions, which may be due to the presence of an interzone-like tissue in the intra-articular space. Study objectives were to further characterize axolotl diarthrodial joint structure and determine the differentiation potential of interzone-like tissue in a skeletal microenvironment.
Diarthrodial joint morphology and expression of aggrecan, brother of CDO (BOC), type I collagen, type II collagen, and growth/differentiation factor 5 (GDF5) were examined in femorotibial joints of sexually mature (>12 months) axolotls. Joint tissue cellularity was evaluated in individuals from 2 to 24 months of age. Chondrogenic potential of the interzone was evaluated by placing interzone-like tissue into 4 mm tibial defects.
Cavitation reached completion in the femoroacetabular and humeroradial joints, but an interzone-like tissue was retained in the intra-articular space of distal limb joints. Joint tissue cellularity decreased to 7 months of age and then remained stable. Gene expression patterns of joint markers are broadly similar in developing mammals and mature axolotls. When interzone-like tissue was transplanted into critical size skeletal defects, an accessory joint developed within the defect site.
These experiments indicate that mature axolotl diarthrodial joints are phenotypically similar to developing synovial joints in mammals. Generation of an accessory joint by interzone-like tissue suggests multipotent cellular differentiation potential similar to that of interzone cells in the mammalian fetus. The data support the axolotl as a novel vertebrate model for joint development and repair.
了解指导关节发育的机制可能有助于理解关节病变和确定新的治疗方法。我们之前已经证实,蝾螈可以完全修复大的关节软骨损伤,这可能是由于关节内空间存在类似间充质的组织。研究目的是进一步描述蝾螈关节的结构,并确定在骨骼微环境中类似间充质的组织的分化潜力。
在性成熟(>12 个月)蝾螈的股胫关节中检查了关节形态和聚集蛋白、CDO 兄弟(BOC)、I 型胶原、II 型胶原和生长/分化因子 5(GDF5)的表达。评估了 2 至 24 个月个体的关节组织细胞密度。通过将类似间充质的组织放入 4 毫米胫骨缺损中来评估间充质的软骨形成潜力。
在股骨髋臼和肱桡关节中,空化完成,但在远端肢体关节的关节内空间中保留了类似间充质的组织。关节组织细胞密度在 7 个月大时下降,然后保持稳定。关节标志物的基因表达模式在发育中的哺乳动物和成熟的蝾螈中大致相似。当类似间充质的组织被移植到临界大小的骨骼缺损中时,在缺损部位形成了一个副关节。
这些实验表明,成熟的蝾螈关节在表型上与发育中的哺乳动物滑膜关节相似。类似间充质组织产生副关节表明其具有多能细胞分化潜力,类似于哺乳动物胎儿中的间充质细胞。这些数据支持蝾螈作为关节发育和修复的新型脊椎动物模型。