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Zinc deficiency decreases osteoblasts and osteoclasts associated with the reduced expression of Runx2 and RANK.

机译:缺锌会减少成骨细胞和破骨细胞,并降低Runx2和RANK的表达。

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The effects of Zinc(Zn)-deficiency on the function and differentiation of osteoblasts and osteoclasts were investigated in vivo using rats, which were fed a Zn-adequate (control) or Zn-free diet (ZD) or pair-fed a Zn-adequate diet (PF) for 3 weeks. Levels of Zn, insulin, insulin-like growth factor I (IGF-I), and osteoclacin in serum and the activities and numbers of osteoblasts and osteoclasts in bone decreased in ZD rats compared with the control and PF rats. The frequency analyses showed that the precursors of osteoblasts and osteoclasts decreased in bone marrow of ZD, but not PF, rats. The expression of receptor for activation of NF-kappaB (RANK) decreased with the Zn-deficiency, although RANK ligand, osteoprotegerin, macrophage colony-stimulating factor, and c-fms levels were unaltered. The protein level of a transcription factor MITF, but not PU.1, decreased. The expression of Runx2 decreased associated with the decrease in beta-catenin protein and the suppression of glycogen synthase kinase 3beta (GSK3beta) inhibition and Akt activation. The gene expression of the insulin receptor, IGF-I and the IGF-I receptor was decreased with a reduced level of transcription factor SP-1. These results suggested that a deficiency of Zn decreased osteoclastogenesis associated with the reduced expression of RANK through a decrease in MITF protein, and osteoblastogenesis associated with the reduced expression of Runx2 through the inhibition of Wnt/beta-catenin signaling via the suppression of GSK3beta inhibition and Akt activation preceded by the reduced level of SP-1 protein.
机译:体内缺锌(Zn)对成骨细胞和破骨细胞功能和分化的影响已通过使用大鼠进行了体内研究,这些大鼠被喂食了充足的锌(对照)或无锌饮食(ZD)或成对饲喂锌。持续3周的适当饮食(PF)。与对照组和PF大鼠相比,ZD大鼠血清中的Zn,胰岛素,胰岛素样生长因子I(IGF-1)和骨锁骨素水平以及骨中成骨细胞和破骨细胞的活性和数量均降低。频率分析表明,ZD大鼠的骨髓中成骨细胞和破骨细胞的前体减少,而PF大鼠则没有。锌缺乏时,激活NF-κB(RANK)的受体表达降低,尽管RANK配体,骨保护素,巨噬细胞集落刺激因子和c-fms水平未改变。转录因子MITF的蛋白质水平下降,但PU.1下降。 Runx2的表达减少与β-catenin蛋白的减少以及糖原合酶激酶3beta(GSK3beta)抑制和Akt激活的抑制有关。胰岛素受体,IGF-1和IGF-1的基因表达随转录因子SP-1的降低而降低。这些结果表明,锌缺乏通过MITF蛋白的减少而与RANK的表达减少相关的成骨细胞减少,以及通过抑制WSK /β-catenin信号通过抑制GSK3beta和抑制Wnt /β-catenin的表达而与Runx2的表达减少相关的成骨细胞。 Akt激活之前的SP-1蛋白水平降低。

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