Department of Cell Developmental and Integrative Biology, University of Alabama at Birmingham, AL, USA; Department of Orthopaedic Surgery, Washington University, St. Louis, MO, USA.
Department of Cell Developmental and Integrative Biology, University of Alabama at Birmingham, AL, USA.
Dev Biol. 2022 Aug;488:120-130. doi: 10.1016/j.ydbio.2022.05.013. Epub 2022 May 26.
We previously showed the importance of TGFβ signaling in development of the mouse axial skeleton. Here, we provide the first direct evidence that TGFβ signaling is required for resegmentation of the sclerotome using chick embryos. Lipophilic fluorescent tracers, DiO and DiD, were microinjected into adjacent somites of embryos treated with or without TGFβRI inhibitors, SB431542, SB525334 or SD208, at developmental day E2.5 (HH16). Lineage tracing of labeled cells was observed over the course of 4 days until the completion of resegmentation at E6.5 (HH32). Vertebrae were malformed and intervertebral discs were small and misshapen in inhibitor injected embryos. Hypaxial myofibers were also increased in thickness after treatment with the inhibitor. Inhibition of TGFβ signaling resulted in alterations in resegmentation that ranged between full, partial, and slanted shifts in distribution of DiO or DiD labeled cells within vertebrae. Patterning of rostro-caudal markers within sclerotome was disrupted at E3.5 after treatment with TGFβRI inhibitor with rostral domains expressing both rostral and caudal markers. We propose that TGFβ signaling regulates rostro-caudal polarity and subsequent resegmentation in sclerotome during spinal column development.
我们之前已经证明了 TGFβ 信号通路在小鼠轴性骨骼发育中的重要性。在这里,我们首次提供了直接证据,表明 TGFβ 信号通路对于使用鸡胚的体节重新分割是必需的。亲脂性荧光示踪剂 DiO 和 DiD 在 TGFβRI 抑制剂 SB431542、SB525334 或 SD208 处理或未处理的胚胎 E2.5(HH16)时被微注射到相邻的体节中。在 E6.5(HH32)完成重新分割的过程中,观察了标记细胞的谱系追踪。在抑制剂注射的胚胎中,椎体畸形,椎间盘小且畸形,肌肉纤维也变厚。TGFβ 信号通路的抑制导致重新分割发生改变,在 DiO 或 DiD 标记细胞在椎体中的分布上,完全、部分和倾斜的分布变化。在 TGFβRI 抑制剂处理后,E3.5 时体节内的头尾标记物的模式被打乱,头区表达头区和尾区的标记物。我们提出,TGFβ 信号通路在脊柱发育过程中调节体节的头尾极性和随后的重新分割。