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High glucose alters the secretome of mechanically stimulated osteocyte-like cells affecting osteoclast precursor recruitment and differentiation

机译:高血糖会改变机械刺激的类骨细胞样细胞的分泌组,从而影响破骨细胞前体的募集和分化

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摘要

Diabetes mellitus (DM) induces bone deterioration, while mechanical stimulation promotes osteocyte-driven bone formation. We aimed to evaluate the interaction of acute exposure (24 h) to high glucose (HG) with both the pro-survival effect conferred to osteocytic MLO-Y4 cells and osteoblastic MC3T3-E1 cells by mechanical stimulation and the interaction of these cells with osteoclast precursor RAW264.7 cells. We found that 24 h of HG (25 mM) preexposure prevented both cell survival and ERK and β-catenin nuclear translocation upon mechanical stimulation by fluid flow (FF) (10 min) in both MLO-Y4 and MC3T3-E1 cells. However, migration of RAW 264.7 cells was inhibited by MLO-Y4 cell-conditioned medium (CM), but not by MC3T3-E1 cell-CM, with HG or FF. This inhibitory effect was associated with consistent changes in VEGF, RANTES, MIP-1α, MIP-1β MCP-1, and GM-CSF in MLO-Y4 cellCM. RAW264.7 proliferation was inhibited by MLO-Y4 CM under static or HG conditions, but it increased by FF-CM with or without HG. In addition, both FF and HG abrogated the capacity of RAW 264.7 cells to differentiate into osteoclasts, but in a different manner. Thus, HG-CM in static condition allowed formation of osteoclast-like cells, which were unable to resorb hydroxyapatite. In contrast, FF-CM prevented osteoclastogenesis even in HG condition. Moreover, HG did not affect basal RANKL or IL-6 secretion or their inhibition induced by FF in MLO-Y4 cells. In conclusion, this in vitro study demonstrates that HG exerts disparate effects on osteocyte mechanotransduction, and provides a novel mechanism by which DM disturbs skeletal metabolism through altered osteocyte-osteoclast communication.
机译:糖尿病(DM)会导致骨骼退化,而机械刺激会促进骨细胞驱动的骨骼形成。我们旨在评估通过机械刺激急性暴露(24 h)与高糖(HG)的相互作用与成骨细胞MLO-Y4细胞和成骨细胞MC3T3-E1细胞的促存活作用以及这些细胞与破骨细胞的相互作用RAW264.7前体细胞。我们发现,在MLO-Y4和MC3T3-E1细胞中,通过流体流动(FF)(10分钟)进行机械刺激后,HG(25 mM)的24 h预暴露均阻止了细胞存活以及ERK和β-catenin核易位。但是,RAW 264.7细胞的迁移受MLO-Y4细胞条件培养基(CM)抑制,但不受MC3T3-E1细胞CM和HG或FF抑制。这种抑制作用与MLO-Y4 cellCM中VEGF,RANTES,MIP-1α,MIP-1βMCP-1和GM-CSF的一致变化有关。 RAW264.7增殖在静态或HG条件下被MLO-Y4 CM抑制,但在有或没有HG的情况下,FF-CM均能提高RAW264.7的增殖。此外,FF和HG均废除了RAW 264.7细胞分化为破骨细胞的能力,但方式不同。因此,处于静止状态的HG-CM允许形成破骨细胞样细胞,其不能吸收羟磷灰石。相反,FF-CM即使在HG条件下也能阻止破骨细胞生成。此外,HG在MLO-Y4细胞中不影响基础RANKL或IL-6分泌或FF诱导的抑制作用。总之,这项体外研究表明,HG对骨细胞机械转导具有不同的作用,并提供了DM通过改变骨细胞-破骨细胞通讯来干扰骨骼代谢的新机制。

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