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亚毒浓度镉对骨基因表达谱的影响:一项体外研究的结果。

Effects of sub-toxic Cadmium concentrations on bone gene expression program: results of an in vitro study.

机构信息

Department of Experimental Medicine and Biochemistry, University of Perugia, Perugia, Italy.

出版信息

Toxicol In Vitro. 2010 Sep;24(6):1670-80. doi: 10.1016/j.tiv.2010.05.020. Epub 2010 Jun 4.

DOI:10.1016/j.tiv.2010.05.020
PMID:20570719
Abstract

Since occupational and environmental exposure to the heavy metal Cadmium (Cd) affects human health this study investigated the effects of exposure to a single, or multiple, sub-toxic Cd concentrations on sub-confluent and confluent human osteoblast growth and expression of specific bone differentiation markers. RT-PCR quantified gene expression of type I collagen, metalloprotease (MMP13), runt-related transcription factor-2 (RUNX2), osterix, osteocalcin, osteonectin, alkaline phosphatase, integrins and bone sialoprotein (BSP). Expression of fibroblast growth factors 1 and 2 (FGF1, FGF2), transforming growth factor-beta(3) (TGFbeta(3)) and bone morphogenetic protein-2 (BMP2) were also evaluated to determine whether Cd-related effects were mediated by an imbalance in expression. Depending on osteoblast concentration and maturation stages, Cd inhibited or stimulated cell growth, decreased type I collagen, increased MMP13, FGF1 and BMP2 gene expression and stimulated the mineralization process only in continuously exposed cultures. These results suggest that in vivo, acute or chronic exposure to sub-toxic Cd concentrations may affect bone formation differently and support the hypothesis that Cd-induced bone disorders may involve downstream changes in growth factor expression. The results are of interest in forensic and occupational medicine in establishing preventive measures to reduce professional exposure risks.

摘要

由于职业和环境接触重金属镉(Cd)会影响人类健康,因此本研究调查了暴露于单一或多种亚毒性 Cd 浓度对亚汇合和汇合人成骨细胞生长和特定骨分化标志物表达的影响。RT-PCR 定量测定了 I 型胶原、金属蛋白酶(MMP13)、转录因子-2(RUNX2)、成骨细胞特异性转录因子 2(osterix)、骨钙素、骨粘连蛋白、碱性磷酸酶、整合素和骨唾液蛋白(BSP)的基因表达。还评估了成纤维细胞生长因子 1 和 2(FGF1、FGF2)、转化生长因子-β(3)(TGFbeta(3))和骨形态发生蛋白-2(BMP2)的表达,以确定 Cd 相关作用是否是由表达失衡介导的。根据成骨细胞浓度和成熟阶段的不同,Cd 抑制或刺激细胞生长,降低 I 型胶原的表达,增加 MMP13、FGF1 和 BMP2 的基因表达,并仅在持续暴露的培养物中刺激矿化过程。这些结果表明,在体内,急性或慢性暴露于亚毒性 Cd 浓度可能会以不同的方式影响骨形成,并支持 Cd 诱导的骨疾病可能涉及生长因子表达的下游变化的假说。这些结果在法医和职业医学中具有重要意义,有助于制定预防措施以降低职业暴露风险。

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