Huang Feng, Hu Xiaoxiao, Fang Chunni, Liu Hong, Lin Chensheng, Zhang Yanding, Hu Xuefeng
Center for Biomedicine Research of South China, Fujian Key Laboratory of Developmental and Neuro Biology, College of Life Science, Fujian Normal University, Fuzhou, 350108, Fujian, People's Republic of China.
Histochem Cell Biol. 2015 Nov;144(5):457-69. doi: 10.1007/s00418-015-1358-7. Epub 2015 Aug 13.
Mammalian tooth development is regulated by paracrine signal molecules of several conserved family interactions between epithelium and mesenchyme. The expression patterns and regulative roles of FGF signaling have been extensively studied in the mouse odontogenesis; however, that is not well known in human tooth development. In order to unveil the molecular mechanisms that regulate human tooth morphogenesis, we examined the expression patterns of the critical molecules involved in FGF signaling pathway in the developing human tooth germ by in situ hybridization, immunohistochemistry, and real-time RT-PCR, including FGF ligands, receptors, and intracellular transducer. We found overlapping but distinct expression pattern of FGF ligands and receptors in the different stages and components. Expression of FGF4, FGF7, FGF8, and FGF9 persists widespread in human tooth mesenchyme, which is quite different to that of in mouse. FGFR1 may be the major receptor in regulate mechanisms of FGF signals in human tooth development. Real-time RT-PCR indeed confirmed the results of in situ hybridization. Results of K-Ras, p-ERK1/2, p-p38, p-JNK, and p-PDK1 expression reveal spatial and temporal patterns of FGF signaling during morphogenesis and organogenesis of human tooth germ. Activity of the FGF signaling transducer protein in human tooth germ was much higher than that of in mouse. Our results provided important FGF singling information in the developing process, pinpoint to the domains where the downstream target genes of FGF signaling can be sought, and enlightened our knowledge about the nature of FGF signaling in human tooth germ.
哺乳动物牙齿发育受上皮和间充质之间几种保守家族相互作用的旁分泌信号分子调控。FGF信号的表达模式和调控作用在小鼠牙齿发生过程中已得到广泛研究;然而,在人类牙齿发育中却不太清楚。为了揭示调控人类牙齿形态发生的分子机制,我们通过原位杂交、免疫组织化学和实时RT-PCR检测了人类发育中牙胚FGF信号通路相关关键分子的表达模式,包括FGF配体、受体和细胞内转导分子。我们发现在不同阶段和成分中FGF配体和受体的表达模式有重叠但又不同。FGF4、FGF7、FGF8和FGF9在人类牙间充质中持续广泛表达,这与小鼠中的情况有很大不同。FGFR1可能是人类牙齿发育中FGF信号调控机制的主要受体。实时RT-PCR确实证实了原位杂交的结果。K-Ras、p-ERK1/2、p-p38、p-JNK和p-PDK1的表达结果揭示了人类牙胚形态发生和器官发生过程中FGF信号的时空模式。人类牙胚中FGF信号转导蛋白的活性远高于小鼠。我们的结果提供了人类牙齿发育过程中重要的FGF信号信息,指出了可寻找FGF信号下游靶基因的区域,并增进了我们对人类牙胚中FGF信号本质的认识。