首页> 美国卫生研究院文献>Frontiers in Physiology >RNA-Sequencing Analyses Demonstrate the Involvement of Canonical Transient Receptor Potential Channels in Rat Tooth Germ Development
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RNA-Sequencing Analyses Demonstrate the Involvement of Canonical Transient Receptor Potential Channels in Rat Tooth Germ Development

机译:RNA测序分析表明典型的瞬态受体潜在通道在大鼠牙胚发育中的参与。

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摘要

Tooth development depends on multiple molecular interactions between the dental epithelium and mesenchyme, which are derived from ectodermal and ectomesenchymal cells, respectively. We report on a systematic RNA sequencing analysis of transcriptional expression levels from the bud to hard tissue formation stages of rat tooth germ development. We found that GNAO1, ENO1, EFNB1, CALM1, SIAH2, ATP6V0A1, KDELR2, GTPBP1, POLR2C, SORT1, and members of the canonical transient receptor potential (TRPC) channel family are involved in tooth germ development. Furthermore, Cell Counting Kit 8 (CCK8) and Transwell migration assays were performed to explore the effects of these differentially expressed genes (DEGs) on the proliferation and migration of dental pulp stem cells. Immunostaining revealed that TRPC channels are expressed at varying levels during odontogenesis. The identified genes represent novel candidates that are likely to be vital for rat tooth germ development. Together, the results provide a valuable resource to elucidate the gene regulatory mechanisms underlying mammalian tooth germ development.
机译:牙齿发育取决于牙齿上皮和间充质之间的多种分子相互作用,它们分别源自外胚层和外胚层细胞。我们报告了从芽到大鼠牙胚发育的硬组织形成阶段的转录表达水平的系统RNA测序分析。我们发现GNAO1,ENO1,EFNB1,CALM1,SIAH2,ATP6V0A1,KDELR2,GTPBP1,POLR2C,SORT1和规范的瞬时受体电位(TRPC)通道家族成员都参与了牙胚的发育。此外,进行了细胞计数试剂盒8(CCK8)和Transwell迁移分析,以探讨这些差异表达基因(DEG)对牙髓干细胞增殖和迁移的影响。免疫染色显示,在牙本质发生过程中,TRPC通道以不同水平表达。鉴定出的基因代表了可能对大鼠牙胚发育至关重要的新候选物。在一起,结果提供了宝贵的资源,阐明了潜在的哺乳动物牙胚发育的基因调控机制。

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