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首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Induction of apoptosis in murine clonal osteoblasts expressed by human T-cell leukemia virus type I tax by NF-kappa B and TNF-alpha.
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Induction of apoptosis in murine clonal osteoblasts expressed by human T-cell leukemia virus type I tax by NF-kappa B and TNF-alpha.

机译:通过NF-κB和TNF-α诱导人I型T细胞白血病病毒表达的鼠类克隆成骨细胞凋亡。

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We investigated the effects of various cytokines in the presence of human T-cell leukemia virus type I (HTLV-I) tax protein in murine clonal osteoblasts, MC3T3-E1 cells. Skeletal remodeling by osteoclasts and osteoblasts is coordinated by cytokines, which are activated by HTLV-I tax protein via nuclear factor-kappa B (NF-kappa B). MC3T3-E1 cells were cocultured with an irradiated HTLV-I-producing lymphocyte cell line, MT-2. After coculture, the tumor necrosis factor-alpha (TNF-alpha) level in the medium was markedly elevated during the 7 days of culture, and MC3T3-E1 cells underwent apoptotic cell death. Marked apoptosis was also observed in MC3T3-E1 cells treated with MT-2 culture medium and in HTLV-I tax-expressing MC3T3-E1 clones, which both expressed high levels of TNF-alpha. This apoptosis was prevented by treatment with neutralizing anti-TNF-alpha antibody (alpha TNF). HTLV-I tax protein and TNF-alpha induced activation of NF-kappa B in apoptotic MC3T3-E1 cells. Decreased NF-kappa B activation was observed in HTLV-I tax-expressing MC3T3-E1 cells treated with alpha TNF. Our results suggest that HTLV-I tax activated NF-kappa B and subsequently TNF-alpha, leading to apoptosis of osteoblasts.
机译:我们在鼠类克隆成骨细胞MC3T3-E1细胞中研究了存在人I型T细胞白血病病毒(HTLV-1)税收蛋白的情况下各种细胞因子的作用。破骨细胞和成骨细胞的骨骼重塑由细胞因子协调,细胞因子被HTLV-1税蛋白通过核因子-κB(NF-κB)激活。将MC3T3-E1细胞与经辐射的产生HTLV-1的淋巴细胞MT-2共培养。共培养后,在培养的7天中,培养基中的肿瘤坏死因子-α(TNF-α)水平显着升高,并且MC3T3-E1细胞发生了凋亡。在用MT-2培养基处理过的MC3T3-E1细胞和表达HTLV-1税收的MC3T3-E1克隆中也观察到明显的凋亡,它们均表达高水平的TNF-α。通过用中和性抗TNF-α抗体(αTNF)来防止这种凋亡。 HTLV-1税收蛋白和TNF-α诱导凋亡的MC3T3-E1细胞中NF-κB的活化。在用αTNF处理的表达HTLV-1税收的MC3T3-E1细胞中观察到NF-κB激活减少。我们的结果表明,HTLV-1激活NF-κB,然后激活TNF-α,导致成骨细胞凋亡。

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