Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México Ciudad Universitaria, Apartado Postal 70228, Mexico.
Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México Ciudad Universitaria, Apartado Postal 70228, Mexico.
Dev Biol. 2021 Jan 1;469:86-95. doi: 10.1016/j.ydbio.2020.10.003. Epub 2020 Oct 12.
During digit development, the correct balance of chondrogenic signals ensures the recruitment of undifferentiated cells into the cartilage lineage or the maintenance of cells at the undifferentiated stage. WNT/β catenin maintains the pool of progenitor cells, whereas TGFβ signalling promotes cartilage differentiation by inducing Sox9 expression. Moreover, WNT5A promotes the degradation of β catenin during mouse limb development. Although these mechanisms are well established, it is still unknown whether the signalling pathway downstream WNT5A is also involved in early chondrogenesis during digit formation. Thus, the aim of this study was to determine the role of WNT5A during the recruitment of progenitor cells during digit development. Our results showed that WNT5A activated calcium (Ca) release in the undifferentiated region during digit development. Further, the blockade of Ca release or calcineurin (CaN) or nuclear factor of activated T-cells (NFAT) functions resulted in an inhibition of cartilage differentiation. Together, our results demonstrate that non canonical WNT5A-Ca-CaN-NFAT signalling plays a key role during embryonic digit development in vivo promoting the competence for chondrogenic signals and also acts as a permissive factor for chondrogenesis independently of cell death mechanisms.
在数字发育过程中,软骨形成信号的正确平衡确保了未分化细胞被招募到软骨谱系中,或者维持细胞处于未分化状态。WNT/β 连环蛋白维持祖细胞池,而 TGFβ 信号通过诱导 Sox9 表达促进软骨分化。此外,WNT5A 在小鼠肢发育过程中促进β 连环蛋白的降解。尽管这些机制已经得到很好的证实,但仍然不清楚 WNT5A 下游的信号通路是否也参与了指形成过程中的早期软骨发生。因此,本研究的目的是确定 WNT5A 在指发育过程中祖细胞募集过程中的作用。我们的结果表明,WNT5A 在指发育过程中未分化区域激活钙(Ca)释放。此外,Ca 释放或钙调神经磷酸酶(CaN)或激活 T 细胞的核因子(NFAT)功能的阻断导致软骨分化的抑制。总之,我们的结果表明,非典型 WNT5A-Ca-CaN-NFAT 信号在体内胚胎指发育过程中发挥关键作用,促进了软骨形成信号的能力,并且独立于细胞死亡机制,作为软骨发生的许可因子。