Department of Orthopaedic Surgery.
Laboratories of Musculoskeletal Orthopedic Research at Einstein-Montefiore (MORE).
Ann N Y Acad Sci. 2019 Apr;1442(1):79-90. doi: 10.1111/nyas.13914. Epub 2018 Jun 28.
The pannexin 1 (Panx1) channel is a mechanosensitive channel that interacts with P2X7 receptors (P2X7R) to form a functional complex that has been shown in vitro to play an essential role in osteocyte mechanosignaling. While the participation of P2X7R in skeletal responses to mechanical loading has been demonstrated, the role of Panx1 and its interplay with P2X7R still remain to be determined. In this study, we use a global Panx1 mouse model and in vivo mechanical loading to demonstrate that Panx1 channels play an essential role in load-induced skeletal responses. We found that absence of Panx1 not only disrupts the P2X7R-Panx1 signaling complex, but also alters load-induced regulation of P2X7R expression. Moreover, lack of Panx1 completely abolished load-induced periosteal bone formation. Load-induced regulation of β-catenin and sclerostin expression was dysregulated in Panx1 , compared to wild-type, bone. This finding suggests that Panx1 deficiency disrupts Wnt/β-catenin signaling by lowering β-catenin while favoring inhibition of bone formation by increasing load-induced sclerostin expression. This study demonstrates the existence of a Panx1-dependent mechanosensitive mechanism that not only modulates ATP signaling but also coordinates Wnt/β-catenin signaling that is essential for proper skeletal response to mechanical loading.
质膜孔蛋白 1(Panx1)通道是一种机械敏感性通道,与 P2X7 受体(P2X7R)相互作用形成一个功能复合物,已在体外证明该复合物在骨细胞机械信号转导中起重要作用。虽然已经证明 P2X7R 参与了骨骼对机械加载的反应,但 Panx1 的作用及其与 P2X7R 的相互作用仍有待确定。在这项研究中,我们使用全局 Panx1 小鼠模型和体内机械加载来证明 Panx1 通道在负荷诱导的骨骼反应中起重要作用。我们发现 Panx1 的缺失不仅破坏了 P2X7R-Panx1 信号复合物,而且改变了负荷诱导的 P2X7R 表达的调节。此外,Panx1 的缺失完全消除了负荷诱导的骨膜骨形成。与野生型相比,Panx1 缺乏的情况下,负荷诱导的β-连环蛋白和硬化素表达的调节被打乱。这一发现表明,Panx1 缺乏通过降低β-连环蛋白而破坏 Wnt/β-连环蛋白信号,同时通过增加负荷诱导的硬化素表达来促进骨形成的抑制。这项研究证明了存在一种依赖 Panx1 的机械敏感性机制,该机制不仅调节 ATP 信号,而且协调 Wnt/β-连环蛋白信号,这对于骨骼对机械加载的适当反应是必不可少的。