Shwartz Yulia, Viukov Sergey, Krief Sharon, Zelzer Elazar
Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.
Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.
Cell Rep. 2016 Jun 21;15(12):2577-87. doi: 10.1016/j.celrep.2016.05.055. Epub 2016 Jun 9.
Synovial joints comprise several tissue types, including articular cartilage, the capsule, and ligaments. All of these compartments are commonly assumed to originate from an early set of Gdf5-expressing progenitors populating the interzone domain. Here, we provide evidence that joints develop through a continuous influx of cells into the interzone, where they contribute differentially to forming joint tissues. Using a knockin Gdf5-CreER(T2) mouse, we show that early labeling of Gdf5-positive interzone cells failed to mark the entire organ. Conversely, multiple Cre activation steps indicated a contribution of these cells to various joint compartments later in development. Spatiotemporal differences between Gdf5 and tdTomato reporter expression support the notion of a continuous recruitment process. Finally, differential contribution of Gdf5-positive cells to various tissues suggests that the spatiotemporal dynamics of Gdf5 expression may instruct lineage divergence. This work supports the influx model of joint development, which may apply to other organogenic processes.
滑膜关节由多种组织类型组成,包括关节软骨、关节囊和韧带。所有这些部分通常被认为起源于一组早期表达Gdf5的祖细胞,这些祖细胞分布在中间带区域。在这里,我们提供证据表明,关节是通过细胞持续流入中间带而发育的,在那里它们对形成关节组织的贡献各不相同。使用敲入Gdf5-CreER(T2)小鼠,我们发现对Gdf5阳性中间带细胞的早期标记未能标记整个器官。相反,多个Cre激活步骤表明这些细胞在发育后期对各种关节部分有贡献。Gdf5和tdTomato报告基因表达之间的时空差异支持了连续招募过程的概念。最后,Gdf5阳性细胞对各种组织的不同贡献表明,Gdf5表达的时空动态可能指导谱系分化。这项工作支持关节发育的流入模型,该模型可能适用于其他器官发生过程。