Department of Neural and Pain Sciences, School of Dentistry, the University of Maryland, Baltimore, MD 21201,USA.
Center to Advance Chronic Pain Research, the University of Maryland, Baltimore, MD 21201,USA.
Development. 2024 May 1;151(9). doi: 10.1242/dev.202386. Epub 2024 May 9.
Piezo1 and Piezo2 are recently reported mechanosensory ion channels that transduce mechanical stimuli from the environment into intracellular biochemical signals in various tissues and organ systems. Here, we show that Piezo1 and Piezo2 display a robust expression during jawbone development. Deletion of Piezo1 in neural crest cells causes jawbone malformations in a small but significant number of mice. We further demonstrate that disruption of Piezo1 and Piezo2 in neural crest cells causes more striking defects in jawbone development than any single knockout, suggesting essential but partially redundant roles of Piezo1 and Piezo2. In addition, we observe defects in other neural crest derivatives such as malformation of the vascular smooth muscle in double knockout mice. Moreover, TUNEL examinations reveal excessive cell death in osteogenic cells of the maxillary and mandibular arches of the double knockout mice, suggesting that Piezo1 and Piezo2 together regulate cell survival during jawbone development. We further demonstrate that Yoda1, a Piezo1 agonist, promotes mineralization in the mandibular arches. Altogether, these data firmly establish that Piezo channels play important roles in regulating jawbone formation and maintenance.
Piezo1 和 Piezo2 是最近报道的机械敏感离子通道,它们将环境中的机械刺激转化为各种组织和器官系统中的细胞内生化信号。在这里,我们表明 Piezo1 和 Piezo2 在颌骨发育过程中表达强烈。神经嵴细胞中 Piezo1 的缺失会导致一小部分但数量显著的小鼠颌骨畸形。我们进一步证明,神经嵴细胞中 Piezo1 和 Piezo2 的破坏会导致颌骨发育中比任何单个敲除更明显的缺陷,这表明 Piezo1 和 Piezo2 具有重要但部分冗余的作用。此外,我们观察到其他神经嵴衍生物的缺陷,如双敲除小鼠血管平滑肌的畸形。此外,TUNEL 检查显示双敲除小鼠上颌和下颌弓的成骨细胞中存在过度的细胞死亡,这表明 Piezo1 和 Piezo2 共同调节颌骨发育过程中的细胞存活。我们进一步证明,Piezo1 激动剂 Yoda1 促进下颌弓的矿化。总之,这些数据确凿地表明 Piezo 通道在调节颌骨形成和维持中发挥重要作用。