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Lysyl oxidase and the lysyl oxidase-like protein modulate odontoblastic differentiation of human dental pulp cells

机译:赖氨酰氧化酶和类似赖氨酰氧化酶的蛋白可调节人牙髓细胞的牙本质细胞分化

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Introduction: The lysyl oxidase (LOX) family is an emerging family of amine oxidases responsible for the formation of collagen fibrils in the extracellular matrix. To date, 5 LOX family genes have been identified in humans, encoding LOX and LOX-like proteins (LOXL, LOXL2, LOXL3, and LOXL4). The goal of this study was to evaluate the expression and function of the LOX family genes in odontoblastic differentiation of human dental pulp (HDP) cells. Methods: Expression of the LOX family genes was assessed by reverse transcriptase polymerase chain reaction analysis, and the amine oxidase activity of HDP cells was evaluated by peroxidase-coupled fluorometric assays. Mineral nodule formation and expression of odontoblastic marker genes were assessed in the presence and absence of specific small interfering RNAs (siRNAs) of the LOX family genes. Results: Among the LOX family genes, only LOX and LOXL showed prominent expression during odontoblastic differentiation of HDP cells. Suppression of LOX and LOXL expression by siRNA-induced interference substantially decreased the amine oxidase activity of the differentiating HDP cells. Furthermore, interference of LOX and LOXL expression inhibited mineral nodule formation and expression of odontoblastic marker genes during odontoblastic differentiation of HDP cells. Conclusions: These findings show for the first time that the LOX- and LOXL-mediated organization of collagen fibrils in extracellular matrices of HDP cells might be an important regulator for odontoblastic differentiation of HDP cells.
机译:简介:赖氨酰氧化酶(LOX)家族是一种新兴的胺氧化酶家族,负责在细胞外基质中形成胶原原纤维。迄今为止,已在人类中鉴定出5个LOX家族基因,它们编码LOX和LOX样蛋白(LOXL,LOXL2,LOXL3和LOXL4)。这项研究的目的是评估LOX家族基因在人类牙髓(HDP)细胞的成牙本质分化中的表达和功能。方法:通过逆转录酶聚合酶链反应分析评估LOX家族基因的表达,并通过过氧化物酶偶联荧光法评估HDP细胞的胺氧化酶活性。在是否存在LOX家族基因的特定小干扰RNA(siRNA)的情况下评估了矿物结节的形成和成牙本质标记基因的表达。结果:在LOX家族基因中,只有LOX和LOXL在HDP细胞的成牙本质细胞分化过程中表现出突出的表达。 siRNA诱导的干扰抑制LOX和LOXL表达大大降低了分化的HDP细胞的胺氧化酶活性。此外,LOX和LOXL表达的干扰抑制了HDP细胞的成牙本质分化过程中的矿物结节形成和成牙本质标记基因的表达。结论:这些发现首次表明,LOX和LOXL介导的HDP细胞胞外基质中胶原纤维的组织可能是HDP细胞牙本质分化的重要调节剂。

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