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Effects of a sulfated exopolysaccharide produced by Altermonas infernus on bone biology

机译:臭豆链霉菌产生的硫酸化胞外多糖对骨骼生物学的影响

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摘要

The growth and differentiation of bone cells is controlled by various factors which can be modulated by heparan sulphates. Here, we investigated the effects of an oversulphated “heparin-like” exopolysaccharide (OS-EPS) on bone. We compared the effect of this compound with that of a native exopolysaccharide (EPS). Long-term administration of OS-EPS causes cancellous bone loss in mice due, in part, to an increase in the number of osteoclasts lining the trabecular bone surface. No significant difference in cancellous bone volume was found between EPS-treated mice and age-matched control mice, underlying the importance of sulphatation in trabecular bone loss. However, the mechanism sustaining this osteoporosis was unclear. To clarify OS-EPS activities, we investigated the effect of OS-EPS in osteogenesis. Our results demonstrated that OS-EPS inhibited osteoclastogenesis in two cell models. By surface plasmon resonance technique we revealed that OS-EPS can constitute a hetero-molecular complex OS-EPS/RANKL/RANK and that RANK had a higher affinity for RANKL pre-incubated with OS-EPS than for RANKL alone which would be in favour of an increase in bone resorption. However, in vitro, OS-EPS inhibit the early steps of osteoclast precursor adhesion and therefore inhibits the step of cell fusion. In addition, we showed that OS-EPS reduces the proliferation and accelerates osteoblastic differentiation, leading to strong inhibition of mineralized nodule formation, which would be in favour of an increase in bone resorption. Taken together, these data show different levels of bone resorption regulation by exopolysaccharides, most of them leading to proresorptive effects.
机译:骨细胞的生长和分化受多种因素控制,这些因素可以被硫酸乙酰肝素调节。在这里,我们研究了过硫酸化的“肝素样”胞外多糖(OS-EPS)对骨骼的影响。我们将该化合物的效果与天然胞外多糖(EPS)的效果进行了比较。长期给予OS-EPS会导致小鼠松质骨丢失,部分原因是衬在小梁骨表面的​​破骨细胞数量增加。在EPS治疗的小鼠和年龄匹配的对照小鼠之间,未发现松质骨体积的显着差异,这说明了硫酸化对小梁骨丢失的重要性。但是,维持这种骨质疏松症的机制尚不清楚。为了阐明OS-EPS的活性,我们调查了OS-EPS在成骨中的作用。我们的结果表明,OS-EPS在两种细胞模型中均抑制破骨细胞生成。通过表面等离振子共振技术,我们发现OS-EPS可以构成异分子复合物OS-EPS / RANKL / RANK,并且RANK对与OS-EPS预孵育的RANKL的亲和力高于单独对RANKL的亲和力,这将是有利的骨吸收增加。然而,在体外,OS-EPS抑制破骨细胞前体粘附的早期步骤,因此抑制了细胞融合的步骤。此外,我们显示OS-EPS减少增殖并加速成骨细胞分化,从而强烈抑制矿化结节的形成,这有利于骨吸收的增加。综上所述,这些数据表明,胞外多糖对骨吸收的调节水平不同,其中大多数会导致吸收作用。

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