Oral Biology and Tissue Regeneration Work Group, Department of Prosthodontics, Medical Faculty, Georg-August-University, Robert Koch Straße 40, 37075, Goettingen, Germany.
Cell Mol Life Sci. 2014 Mar;71(6):1081-96. doi: 10.1007/s00018-013-1436-8. Epub 2013 Aug 4.
Discoidin domain receptor 1 (DDR-1)-deficient mice exhibited a high incidence of osteoarthritis (OA) in the temporomandibular joint (TMJ) as early as 9 weeks of age. They showed typical histological signs of OA, including surface fissures, loss of proteoglycans, chondrocyte cluster formation, collagen type I upregulation, and atypical collagen fibril arrangements. Chondrocytes isolated from the TMJs of DDR-1-deficient mice maintained their osteoarthritic characteristics when placed in culture. They expressed high levels of runx-2 and collagen type I, as well as low levels of sox-9 and aggrecan. The expression of DDR-2, a key factor in OA, was increased. DDR-1-deficient chondrocytes from the TMJ were positively influenced towards chondrogenesis by a three-dimensional matrix combined with a runx-2 knockdown or stimulation with extracellular matrix components, such as nidogen-2. Therefore, the DDR-1 knock-out mouse can serve as a novel model for temporomandibular disorders, such as OA of the TMJ, and will help to develop new treatment options, particularly those involving tissue regeneration.
Discoidin domain receptor 1 (DDR-1)-deficient mice 早在 9 周龄时就表现出颞下颌关节 (TMJ) 骨关节炎 (OA) 的高发病率。它们表现出 OA 的典型组织学特征,包括表面裂缝、糖胺聚糖丧失、软骨细胞簇形成、I 型胶原上调和胶原纤维排列异常。从 DDR-1 缺陷型小鼠 TMJ 分离的软骨细胞在培养中保持其骨关节炎特征。它们表达高水平的 runx-2 和胶原 I,以及低水平的 sox-9 和聚集蛋白聚糖。OA 的关键因子 DDR-2 的表达增加。与三维基质结合使用 runx-2 敲低或刺激细胞外基质成分(如 nidogen-2),可正向影响 TMJ 的 DDR-1 缺陷型软骨细胞向软骨生成分化。因此,DDR-1 敲除小鼠可以作为 TMJ OA 等颞下颌关节紊乱的新型模型,并将有助于开发新的治疗方法,特别是涉及组织再生的方法。