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氟化物在软骨内骨化过程中调节细胞外基质 HSPG 的表达和相关信号通路 FGFR3 以及 Ihh/PTHrP 反馈环。

Fluoride regulates the expression of extracellular matrix HSPG and related signaling pathways FGFR3 and Ihh/PTHrP feedback loop during endochondral ossification.

机构信息

Department of Environmental Health, School of Public Health, China Medical University, No. 77 Puhe Road, Shenyang North New Area, Shenyang, Liaoning Province, PR China.

Department of Environmental Health, School of Public Health, China Medical University, No. 77 Puhe Road, Shenyang North New Area, Shenyang, Liaoning Province, PR China.

出版信息

Environ Toxicol Pharmacol. 2020 Jan;73:103275. doi: 10.1016/j.etap.2019.103275. Epub 2019 Oct 17.

Abstract

Skeletal fluorosis causes growth plate impairment and growth retardation during bone development. Longitudinal bone development is accomplished by endochondral ossification in growth plate. However, the mechanism of fluoride impairs growth plate is unclear. To explore the effect of fluoride on various glycosaminoglycans (GAGs) and related signaling pathways in growth plate during endochondral ossification, SD rats and ATDC5 cells were treated with fluoride and carried out a series of experiments. We found that the expression of heparan sulfate (HS), a kind of GAGs in extracellular matrix, was significantly increased in the growth plate of fluoride-treated rats compared with control rats. Furthermore, the expression of HS synthetic enzyme exostosin 1 (EXT1) and glypican 6 (GPC6), a core protein of HS proteoglycan (HSPG), were significantly increased in fluoride-treated ATDC5 cells compared with control cells (P < 0.05). The expression of related molecules including fibroblast growth factor receptor-3 (FGFR3), signal transducer and activator of transcription 1 (STAT1) and parathyroid hormone-related protein (PTHrP) were significantly increased in the fluoride-treated groups compared with control groups (P < 0.05), and there was significantly decreased in the expression of Indian hedgehog (Ihh) in fluoride-treated groups compared with control groups (P < 0.05). Our data suggested that fluoride increased the content of HSPG in extracellular matrix by promoting the expression of EXT1 and GPC6. Fluoride also activated FGFR3 signaling pathway, inhibited Ihh/PTHrP feedback loop and inhibited endochondral ossification. Nevertheless, the regulation of fluoride on HSPG and related pathways FGFR3 and Ihh/PTHrP feedback loop during endochondral ossification needs to be further studied.

摘要

氟中毒会在骨骼发育过程中导致生长板损伤和生长迟缓。长骨发育是通过生长板的软骨内骨化完成的。然而,氟化物损害生长板的机制尚不清楚。为了探讨氟化物在软骨内骨化过程中对生长板中各种糖胺聚糖(GAGs)和相关信号通路的影响,我们用氟化物处理 SD 大鼠和 ATDC5 细胞并进行了一系列实验。我们发现,与对照组大鼠相比,氟化物处理组大鼠生长板中细胞外基质中肝素硫酸盐(HS)的表达明显增加。此外,与对照组细胞相比,氟化物处理的 ATDC5 细胞中 HS 合成酶外切多糖酶 1(EXT1)和核心蛋白聚糖 6(GPC6)的表达明显增加(P<0.05)。与对照组相比,氟化物处理组中包括成纤维细胞生长因子受体 3(FGFR3)、信号转导和转录激活因子 1(STAT1)和甲状旁腺激素相关蛋白(PTHrP)在内的相关分子的表达明显增加(P<0.05),而氟化物处理组中印度刺猬因子(Ihh)的表达明显降低(P<0.05)。我们的数据表明,氟化物通过促进 EXT1 和 GPC6 的表达增加细胞外基质中 HSPG 的含量。氟化物还激活了 FGFR3 信号通路,抑制了 Ihh/PTHrP 反馈环,抑制了软骨内骨化。然而,氟化物对软骨内骨化过程中 HSPG 及相关通路 FGFR3 和 Ihh/PTHrP 反馈环的调节仍需要进一步研究。

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