Mammoto Tadanori, Mammoto Akiko, Jiang Amanda, Jiang Elisabeth, Hashmi Basma, Ingber Donald E
Vascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, Massachusetts.
Dev Dyn. 2015 Jun;244(6):713-23. doi: 10.1002/dvdy.24264. Epub 2015 Apr 24.
Mechanical compression of cells during mesenchymal condensation triggers cells to undergo odontogenic differentiation during tooth organ formation in the embryo. However, the mechanism by which cell compaction is stabilized over time to ensure correct organ-specific cell fate switching remains unknown.
Here, we show that mesenchymal cell compaction induces accumulation of collagen VI in the extracellular matrix (ECM), which physically stabilizes compressed mesenchymal cell shapes and ensures efficient organ-specific cell fate switching during tooth organ development. Mechanical induction of collagen VI deposition is mediated by signaling through the actin-p38MAPK-SP1 pathway, and the ECM scaffold is stabilized by lysyl oxidase in the condensing mesenchyme. Moreover, perturbation of synthesis or cross-linking of collagen VI alters the size of the condensation in vivo.
These findings suggest that the odontogenic differentiation process that is induced by cell compaction during mesenchymal condensation is stabilized and sustained through mechanically regulated production of collagen VI within the mesenchymal ECM.
在胚胎牙齿器官形成过程中,间充质凝聚期间细胞的机械压缩会触发细胞进行牙源性分化。然而,随着时间推移细胞压实得以稳定以确保正确的器官特异性细胞命运转换的机制仍不清楚。
在此,我们表明间充质细胞压实会诱导细胞外基质(ECM)中VI型胶原蛋白的积累,其在物理上稳定了压缩的间充质细胞形状,并确保在牙齿器官发育过程中实现有效的器官特异性细胞命运转换。VI型胶原蛋白沉积的机械诱导是通过肌动蛋白 - p38丝裂原活化蛋白激酶 - SP1途径的信号传导介导的,并且ECM支架在凝聚的间充质中由赖氨酰氧化酶稳定。此外,VI型胶原蛋白合成或交联的扰动会改变体内凝聚物的大小。
这些发现表明,间充质凝聚期间细胞压实诱导的牙源性分化过程通过间充质ECM内机械调节的VI型胶原蛋白产生得以稳定和持续。