Centre for Osteoarticular and Dental Tissue Engineering, INSERM, U, Nantes, France.
Cell Mol Life Sci. 2011 Jan;68(2):205-18. doi: 10.1007/s00018-010-0527-z. Epub 2010 Sep 17.
Although considerable advances in our understanding of the mechanisms of phosphate homeostasis and skeleton mineralization have recently been made, little is known about the initial events involving the detection of changes in the phosphate serum concentrations and the subsequent downstream regulation cascade. Recent data has strengthened a long-established hypothesis that a phosphate-sensing mechanism may be present in various organs. Such a phosphate sensor would detect changes in serum or local phosphate concentration and would inform the body, the local environment, or the individual cell. This suggests that phosphate in itself could represent a signal regulating multiple factors necessary for diverse biological processes such as bone or vascular calcification. This review summarizes findings supporting the possibility that phosphate represents a signaling molecule, particularly in bone and cartilage, but also in other tissues. The involvement of various signaling pathways (ERK1/2), transcription factors (Fra-1, Runx2) and phosphate transporters (PiT1, PiT2) is discussed.
尽管最近在理解磷酸盐稳态和骨骼矿化机制方面取得了相当大的进展,但对于涉及检测血清磷酸盐浓度变化以及随后的下游调节级联的初始事件知之甚少。最近的数据加强了一个长期存在的假设,即可能存在于各种器官中的磷酸盐感应机制。这种磷酸盐传感器可以检测血清或局部磷酸盐浓度的变化,并向身体、局部环境或单个细胞发出信号。这表明磷酸盐本身可能代表一种信号,调节多种生物过程所必需的多种因素,如骨骼或血管钙化。这篇综述总结了支持磷酸盐作为信号分子的可能性的发现,特别是在骨骼和软骨中,但也在其他组织中。还讨论了涉及各种信号通路(ERK1/2)、转录因子(Fra-1、Runx2)和磷酸盐转运蛋白(PiT1、PiT2)的作用。