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首页> 外文期刊>Journal of periodontal research >The involvement of platelet-derived growth factor receptors and insulin-like growth factor-I receptors signaling during mineralized nodule formation by human periodontal ligament cells.
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The involvement of platelet-derived growth factor receptors and insulin-like growth factor-I receptors signaling during mineralized nodule formation by human periodontal ligament cells.

机译:在人牙周膜细胞矿化结节形成过程中,血小板衍生的生长因子受体和胰岛素样生长因子-I受体信号转导的参与。

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Nemoto E, Shimonishi M, Nitta Y, Shimauchi H. The involvement of platelet-derived growth factor receptors and insulin-like growth factor-I receptors signaling during mineralized nodule formation by human periodontal ligament cells. J Periodont Res 2004; doi: 10.1111/j.1600-0765.2004.00750.x.(c)Blackwell Munksgaard 2004Background and objective: Periodontal ligament cells are regarded to have the capacity to differentiate into cementoblasts or osteoblasts, and are capable of forming a mineralized nodule in vitro. However, the precise mechanisms are unclear. Here we evaluated the possible involvement of growth factor receptors, such as the platelet-derived growth factor receptor (PDGFR), insulin-like growth factor-I receptor (IGF-IR), and epidermal growth factor receptor (EGFR) on periodontal ligament cells and their ligands during periodontal ligament cells differentiation in vitro. Methods: Human periodontal ligament cells were differentiated via culturing in the presence of dexamethasone, ascorbic acid, and beta-glycerophosphate for mineralized nodule formation, characterized by von Kossa staining. Expressions of receptors and their ligands were analyzed by flow cytometry/reverse transcription-polymerase chain reaction. Results: During the differentiation, PDGFR-alpha was held at a lower level compared with the control. PDGFR-beta, however, was maintained at a slightly higher level that was reversed to the control level when mineralized nodules formed. In contrast, IGF-IR and EGFR were not substantially different from the control. The mineralized nodule formation was strongly inhibited by a PDGFR kinase blocker (AG1295 and AG1296), partially inhibited by an IGF-IR kinase blocker (I-Ome-AG538 and AG1024), and not inhibited by an EGFR kinase blocker (AG99). PDGF-A, PDGF-C, PDGF-D, IGF-I, and IGF-II, but not PDGF-B, were expressed on the control as well as dexamethasone/ascorbic acid-treated periodontal ligament cells during mineralized nodule formation; however, the pattern of their expressions was quitedifferent. Conclusion: These findings suggest that a pathway of PDGFs/PDGFR and IGFs/IGF-IR on periodontal ligament cells are involved during mineralized nodule formation, and that PDGFs and IGFs expressed by periodontal ligament cells may contribute to the formation.
机译:Nemoto E,Shimonishi M,Nitta Y,Shimauchi H.在人牙周膜细胞矿化结节形成过程中血小板衍生的生长因子受体和胰岛素样生长因子-I受体的信号传导。 J牙周病杂志2004; doi:10.1111 / j.1600-0765.2004.00750.x。(c)Blackwell Munksgaard 2004背景和目的:牙周膜细胞被认为具有分化为成骨细胞或成骨细胞的能力,并能够在体外形成矿化的结节。但是,确切的机制尚不清楚。在这里,我们评估了牙周膜细胞上可能存在的生长因子受体,例如血小板衍生的生长因子受体(PDGFR),胰岛素样生长因子-I受体(IGF-IR)和表皮生长因子受体(EGFR)及其配体在牙周膜细胞体外分化中的作用方法:通过在地塞米松,抗坏血酸和β-甘油磷酸存在下培养来分化人牙周膜细胞,以形成矿化的结节,其特征在于冯·科萨(von Kossa)染色。通过流式细胞仪/逆转录-聚合酶链反应分析受体及其配体的表达。结果:在分化过程中,PDGFR-α与对照组相比保持较低水平。然而,PDGFR-β维持在稍高的水平,当矿化的结节形成时,PDGFR-β与对照水平相反。相反,IGF-1R和EGFR与对照没有实质性差异。 PDGFR激酶阻滞剂(AG1295和AG1296)强烈抑制矿化的结节形成,IGF-IR激酶阻滞剂(I-Ome-AG538和AG1024)部分抑制,而不被EGFR激酶阻滞剂(AG99)抑制。 PDGF-A,PDGF-C,PDGF-D,IGF-I和IGF-II,而不是PDGF-B,在矿化结节形成过程中在对照以及地塞米松/抗坏血酸处理的牙周膜细胞上表达;然而,他们的表达方式却截然不同。结论:这些发现表明,PDGFs / PDGFR和IGFs / IGF-IR的通路与矿化结节形成有关,而牙周膜细胞表达的PDGFs和IGFs可能参与了该过程。

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