Zhang Yi, Annusver Karl, Sunadome Kazunori, Kameneva Polina, Edwards Steven, Lei Guanghua, Kasper Maria, Chagin Andrei S, Adameyko Igor, Xie Meng
Department of Orthopaedics, Xiangya Hospital, Central South University, Changsha, China.
Department of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Front Cell Dev Biol. 2020 Mar 5;8:122. doi: 10.3389/fcell.2020.00122. eCollection 2020.
A joint connects two or more bones together to form a functional unit that allows different types of bending and movement. Little is known about how the opposing ends of the connected bones are developed. Here, applying various lineage tracing strategies we demonstrate that progenies of Gdf5-, Col2-, Prrx1-, and Gli1-positive cells contribute to the growing epiphyseal cartilage in a spatially asymmetrical manner. In addition, we reveal that cells in the cartilaginous anlagen are likely to be the major sources for epiphyseal cartilage. Moreover, Gli1-positive cells are found to proliferate along the skeletal edges toward the periarticular region of epiphyseal surface. Finally, a switch in the mechanism of growth from cell division to cell influx likely occurs in the epiphyseal cartilage when joint cavitation has completed. Altogether, our findings reveal an asymmetrical mechanism of growth that drives the formation of epiphyseal cartilage ends, which might implicate on how the articular surface of these skeletal elements acquires their unique and sophisticated shape during embryonic development.
关节将两块或多块骨头连接在一起,形成一个功能单元,允许进行不同类型的弯曲和运动。关于相连骨头的相对两端是如何发育的,我们知之甚少。在这里,应用各种谱系追踪策略,我们证明了Gdf5、Col2、Prrx1和Gli1阳性细胞的后代以空间不对称的方式促进生长中的骨骺软骨。此外,我们发现软骨原基中的细胞可能是骨骺软骨的主要来源。此外,发现Gli1阳性细胞沿着骨骼边缘向骨骺表面的关节周围区域增殖。最后,当关节腔形成完成时,骨骺软骨中可能会发生生长机制从细胞分裂向细胞流入的转变。总之,我们的研究结果揭示了一种不对称的生长机制,该机制驱动骨骺软骨末端的形成,这可能暗示了这些骨骼元素的关节表面在胚胎发育过程中如何获得其独特而复杂的形状。