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首页> 外文期刊>Molecular medicine reports >PDGF-BB promotes the differentiation and proliferation of MC3T3-E1 cells through the Src/JAK2 signaling pathway
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PDGF-BB promotes the differentiation and proliferation of MC3T3-E1 cells through the Src/JAK2 signaling pathway

机译:PDGF-BB通过SRC / JAK2信号通路促进MC3T3-E1细胞的分化和增殖

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摘要

Platelet-derived growth factor-BB (PDGF-BB) serves a critical function in human osteoblast differentiation and proliferation. Src and Janus kinase 2 (JAK2) are involved in these processes. In our previous study, it was identified that Src could promote the phosphorylation of JAK2. However, it has yet to be determined whether the Src/JAK2 signaling pathway affects PDGF-BB-mediated osteoblast differentiation and proliferation. In the present study, western blotting, polymerase chain reaction, alizarin red staining, alkaline phosphatase and Cell Counting kit-8 were employed to explore these questions. Firstly, it was demonstrated that PDGF-BB activates the Src/JAK2 signaling pathway in MC3T3-E1 cells in a time-dependent manner. Furthermore, it was demonstrated that PDGF-BB expression promoted MC3T3-E1 cell differentiation and proliferation; this process was suppressed by AG1295, SU6656 and AG490, which are inhibitors of PDGFR-, Src and JAK2, respectively. SU6656 downregulated the activity of Src and JAK2, while AG490 only downregulated JAK2 activity. Therefore, it was concluded that Src is upstream of JAK2. PDGF-BB also upregulated the expression of osteogenesis-associated genes, and the formation of mineral nodules. However, these effects were markedly inhibited by treatment with SU6656. This indicated that PDGF-BB promoted MC3T3-E1 cell differentiation and proliferation by activating the Src/JAK2 signaling pathway. These results suggested that PDGF-BB may have potential applications in the treatment of osteoporosis and bone fractures.
机译:血小板衍生的生长因子-BB(PDGF-BB)在人骨细胞分化和增殖中用于临界功能。 SRC和Janus激酶2(JAK2)参与这些过程。在我们以前的研究中,鉴定了SRC可以促进JAK2的磷酸化。然而,尚不确定SRC / JAK2信号传导途径是否会影响PDGF-BB介导的成骨细胞分化和增殖。在本研究中,使用Western印迹,聚合酶链反应,茜素红染色,碱性磷酸酶和细胞计数套件-8探讨这些问题。首先,证明PDGF-BB以时间依赖的方式在MC3T3-E1细胞中激活SRC / JAK2信号通路。此外,证明PDGF-BB表达促进了MC3T3-E1细胞分化和增殖; AG1295,SU6656和AG490抑制了该方法,分别是PDGFR-,SRC和JAK2的抑制剂。 SU6656下调了SRC和JAK2的活动,而AG490仅下调JAK2活动。因此,得出结论,SRC是JAK2的上游。 PDGF-BB还上调了骨发生相关基因的表达,以及矿物结节的形成。然而,通过用SU6656治疗显着抑制这些效果。这表明PDGF-BB通过激活SRC / JAK2信号通路促进MC3T3-E1细胞分化和增殖。这些结果表明PDGF-BB可能具有潜在的应用,治疗骨质疏松症和骨骨折。

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