Longobardi Lara, Li Tieshi, Tagliafierro Lidia, Temple Joseph D, Willcockson Helen H, Ye Ping, Esposito Alessandra, Xu Fuhua, Spagnoli Anna
Department of Pediatrics, University of North Carolina at Chapel Hill, 109 Mason Farm Road, Chapel Hill, NC, 27599-7039, USA,
Curr Osteoporos Rep. 2015 Feb;13(1):41-51. doi: 10.1007/s11914-014-0247-7.
Synovial joint morphogenesis occurs through the condensation of mesenchymal cells into a non-cartilaginous region known as the interzone and the specification of progenitor cells that commit to the articular fate. Although several signaling molecules are expressed by the interzone, the mechanism is poorly understood. For treatments of cartilage injuries, it is critical to discover the presence of joint progenitor cells in adult tissues and their expression gene pattern. Potential stem cell niches have been found in different joint regions, such as the surface zone of articular cartilage, synovium, and groove of Ranvier. Inherited joint malformations as well as joint-degenerating conditions are often associated with other skeletal defects and may be seen as the failure of morphogenic factors to establish the correct microenvironment in cartilage and bone. Therefore, exploring how joints form can help us understand how cartilage and bone are damaged and develop drugs to reactivate this developing mechanism.
滑膜关节形态发生是通过间充质细胞凝聚成一个称为中间带的非软骨区域以及致力于关节命运的祖细胞的特化来实现的。尽管中间带表达了几种信号分子,但其机制仍知之甚少。对于软骨损伤的治疗,发现成体组织中关节祖细胞的存在及其表达基因模式至关重要。在不同的关节区域已发现潜在的干细胞龛,如关节软骨的表面区域、滑膜和朗飞氏沟。遗传性关节畸形以及关节退变情况通常与其他骨骼缺陷相关,可能被视为形态发生因子未能在软骨和骨中建立正确的微环境。因此,探索关节如何形成有助于我们理解软骨和骨如何受损,并开发药物来重新激活这种发育机制。