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Human Umbilical Cord Mesenchymal Stem Cell Differentiation Into Odontoblast-Like Cells and Endothelial Cells: A Potential Cell Source for Dental Pulp Tissue Engineering

机译:人的脐带间充质干细胞分化成牙卵细胞样细胞和内皮细胞:牙髓组织工程的潜在细胞来源

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摘要

ObjectivesDental pulp regeneration is considered an ideal approach for treating dental pulp disease. Because pulp is composed of various cells, determining the proper seed cells is critical. We explored the potential of human umbilical cord mesenchymal stem cells (hUCMSCs) as seed cells for dental pulp regeneration.MethodsLiquid extract of human treated dentin matrix (LE-TDM) was acquired to culture hUCMSCs. Odontoblast-specific markers were detected by western blot, qRT-PCR, and immunofluorescence assays. Endothelial differentiation of hUCMSCs was examined according to VEGF induction by western blot, qRT-PCR, and Matrigel assays. hUCMSCs and VEGF-induced hUCMSCs (V-hUCMSCs) were also cocultured in vivo for the Matrigel plug assay and in vitro for RNA-sequencing (RNA-seq). Finally, encapsulated mono-cultured hUCMSCs or cocultured hUCMSCs and V-hUCMSCs in scaffolds were injected into the root segments and transplanted into immunodeficient mice for dental pulp regeneration.ResultsUnder LE-TDM induction, hUCMSCs expressed specific odontoblast markers (DSPP, DMP-1, DSP). Under VEGF induction, hUCMSCs expressed functional endothelial markers (CD31, eNOs, vWF). In vivo, the Matrigel plug assay indicated that cocultured hUCMSCs and V-hUCMSCs formed extensive vessel-like structures. RNA-seq results indicated that cocultured V-hUCMSCs exhibited high Hif-1 signaling pathway activity. Both the hUCMSCs mono-culture and coculture groups showed pulp-like tissue regeneration. The cocultured group showed more extracellular matrix and vascularization than the mono-cultured group in vivo.ConclusionhUCMSCs can differentiate into odontoblast-like cells and functional endothelial cells. Cocultured hUCMSCs and V-hUCMSCs formed vessel-like structures and regenerated dental pulp-like tissue. Therefore, hUCMSCs can be used as an alternative seed cell source for angiogenesis and dental pulp regeneration.
机译:ObjectivesDental纸浆再生被认为是治疗牙体牙髓病的理想方法。因为纸浆是由各种细胞的,确定合适的种子细胞是至关重要的。我们探讨人脐带的电位间充质干细胞(hUCMSCs)作为种子细胞用于人类牙本质基质(LE-TDM)处理的牙髓regeneration.MethodsLiquid萃取液获得的培养hUCMSCs。特异性标记成牙本质通过免疫印迹,定量RT-PCR和免疫荧光测定法来检测。 hUCMSCs的内皮分化是根据由免疫印迹,定量RT-PCR,和Matrigel测定VEGF诱导检查。 hUCMSCs和VEGF诱导的hUCMSCs(V-hUCMSCs)也共培养在体内基质胶塞测定和体外用于RNA测序(RNA-SEQ)。最后,在支架包封的单培养hUCMSCs或共培养hUCMSCs和V-hUCMSCs分别注入根段,并移植到免疫缺陷小鼠对牙髓regeneration.ResultsUnder LE-TDM诱导,表达特定牙本质标记(DSPP,DMP-1 hUCMSCs, DSP)。下VEGF诱导,表达hUCMSCs官能内皮标志物(CD31,ENOS,vWF)的。在体内,基质胶塞测定表明形成血管样结构的广泛的是共培养hUCMSCs和V-hUCMSCs。 RNA-SEQ结果表明,共培养的V-hUCMSCs显示出高的HIF-1信号传导途径的活性。两者hUCMSCs单 - 培养呈纸浆状组织再生和共培养基。共培养组显示多种细胞外基质和血管比vivo.ConclusionhUCMSCs单培养的组能分化成成牙本质细胞样细胞和功能性内皮细胞。共培养hUCMSCs和V-hUCMSCs形成血管样结构和再生纸浆样组织的牙科。因此,hUCMSCs可作为血管生成和牙髓再生的替代种子细胞来源。

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