Department of Oncology and Metabolism, Mellanby Centre for Bone Research, University of Sheffield, Sheffield, United Kingdom.
Department of Neuroscience, Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield, Sheffield, United Kingdom.
Front Endocrinol (Lausanne). 2020 Sep 24;11:581002. doi: 10.3389/fendo.2020.581002. eCollection 2020.
Local site-specific differences between bones in different regions of the skeleton account for their different properties and functions. To identify mechanisms behind these differences, we have performed a cross-species study comparing RNA transcriptomes of cranial and tibial osteocytes, from bones with very different primary functions and physiological responses, collected from the same individual mouse, rat, and rhesus macaque. Bioinformatic analysis was performed to identify 32 genes changed in the same direction between sites and shared across all three species. Several well-established key genes in bone growth and remodeling were upregulated in the tibias of all three species (BMP7, DKK1, FGF1, FRZB, SOST). Many of them associate or crosstalk with the Wnt signaling pathway. These results suggest Wnt signaling-related candidates for different control of regulatory mechanisms in bone homeostasis in the skull and tibia and indicate a different balance between genetically determined structure and feedback mechanisms to strains induced by mechanical loading at the different sites.
骨骼不同区域的局部位置特异性差异导致了它们具有不同的特性和功能。为了确定这些差异背后的机制,我们进行了一项跨物种研究,比较了来自同一只小鼠、大鼠和恒河猴的具有非常不同主要功能和生理反应的颅骨和胫骨骨细胞的 RNA 转录组。生物信息学分析用于鉴定在 32 个基因在方向上发生变化并在所有三个物种中共享的基因。几个在骨骼生长和重塑中确立的关键基因在所有三个物种的胫骨中均上调(BMP7、DKK1、FGF1、FRZB、SOST)。其中许多与 Wnt 信号通路相关或相互作用。这些结果表明,Wnt 信号相关候选基因可能对颅骨和胫骨中骨稳态的调控机制有不同的控制,并表明不同部位的机械加载引起的遗传结构和反馈机制之间存在不同的平衡。