Khan I M, Redman S N, Williams R, Dowthwaite G P, Oldfield S F, Archer C W
Cardiff School of Biosciences, Cardiff University, Cardiff CF103US, Wales, United Kingdom.
Curr Top Dev Biol. 2007;79:1-36. doi: 10.1016/S0070-2153(06)79001-9.
During vertebrate evolution, successful adaptation of animal limbs to a variety of ecological niches depended largely on the formation and positioning of synovial joints. The function of a joint is to allow smooth articulation between opposing skeletal elements and to transmit biomechanical loads through the structure, and this is achieved through covering the ends of bones with articular cartilage, lubricating the joint with synovial fluid, using ligaments to bind the skeletal elements together, and encapsulating the joint in a protective fibrous layer of tissue. The diversity of limb generation has been proposed to occur through sequential branching and segmentation of precartilaginous skeletal elements along the proximodistal axis of the limb. The position of future joints is first delimited by areas of higher cell density called interzones initially through an as yet unidentified inductive signal, subsequently specification of these regions is controlled hierarchically by wnt14 and gdf5, respectively. Joint-forming cell fate although specified is not fixed, and joints will fuse if growth factor signaling is perturbed. Cavitation, the separation of the two opposing skeletal elements, and joint morphogenesis, the process whereby the joint cells organize and mature to establish a functional interlocking and reciprocally shaped joint, are slowly being unraveled through studying the plethora of molecules that make up the unique extracellular matrix of the forming structure. The joint lining tissue, articular cartilage, is avascular, and this limits its reparative capacity such that arthritis and associated joint pathologies are the single largest cause of disability in the adult population. Recent discoveries of adult stem cells and more specifically the isolation of chondroprogenitor cells from articular cartilage are extending available therapeutic options, though only with a more complete understanding of synovial joint development can such options have greater chances of success.
在脊椎动物进化过程中,动物肢体成功适应各种生态位在很大程度上取决于滑膜关节的形成和定位。关节的功能是使相对的骨骼元件之间实现平滑的关节活动,并通过该结构传递生物力学负荷,这是通过用关节软骨覆盖骨头末端、用滑液润滑关节、用韧带将骨骼元件绑定在一起以及将关节包裹在保护性纤维组织层中来实现的。肢体生成的多样性被认为是通过沿肢体近远轴的软骨前骨骼元件的顺序分支和分割而发生的。未来关节的位置首先由称为中间带的细胞密度较高的区域界定,最初是通过一种尚未确定的诱导信号,随后这些区域的特化分别由wnt14和gdf5分层控制。尽管关节形成细胞命运已被指定,但并非固定不变,如果生长因子信号受到干扰,关节将会融合。通过研究构成形成结构独特细胞外基质的大量分子,空化(即两个相对骨骼元件的分离)和关节形态发生(即关节细胞组织和成熟以建立功能性互锁和相互塑形关节的过程)正逐渐被揭示。关节衬里组织,即关节软骨,是无血管的,这限制了其修复能力,使得关节炎和相关关节疾病成为成年人群残疾的单一最大原因。成体干细胞的最新发现,更具体地说是从关节软骨中分离出软骨祖细胞,正在扩展可用的治疗选择,不过只有更全面地了解滑膜关节发育,这些选择才有更大的成功机会。