Department of Oral Cell Biology, ACTA-University of Amsterdam and VU University Amsterdam, MOVE Research Institute Amsterdam, Amsterdam, The Netherlands.
J Dent Res. 2014 Apr;93(4):394-9. doi: 10.1177/0022034514522485. Epub 2014 Feb 3.
Mechanosensitive osteocytes regulate bone mass in adults. Interleukin 6 (IL-6), such as present during orthodontic tooth movement, also strongly affects bone mass, but little is known about the effect of IL-6 on osteocyte function. Therefore we aimed to determine in vitro whether IL-6 affects osteocyte mechanosensitivity, and osteocyte regulation of osteoclastogenesis and osteoblast differentiation. MLO-Y4 osteocytes were incubated with/without IL-6 (1 or 10 pg/mL) for 24 hr. Subsequently, osteocytes were subjected to mechanical loading by pulsating fluid flow (PFF) for 1 hr. Mouse osteoclast precursors were cultured for 7 days on top of IL-6-treated osteocytes. Conditioned medium from osteocytes treated with/without IL-6 was added to MC3T3-E1 pre-osteoblasts for 14 days. Exogenous IL-6 (10 pg/mL) did not alter the osteocyte response to PFF. PFF significantly enhanced IL-6 production by osteocytes. IL-6 enhanced Rankl expression but reduced caspase 3/7 activity by osteocytes, and therefore did not affect osteocyte-stimulated osteoclastogenesis. Conditioned medium from IL-6-treated osteocytes reduced alkaline phosphatase (ALP) activity and Runx2 expression in osteoblasts, but increased expression of the proliferation marker Ki67 and osteocalcin. Our results suggest that IL-6 is produced by shear-loaded osteocytes and that IL-6 may affect bone mass by modulating osteocyte communication toward osteoblasts.
机械敏感的破骨细胞调节成骨细胞的骨量。白细胞介素 6(IL-6),如在正畸牙齿移动期间存在,也强烈影响骨量,但对于 IL-6 对破骨细胞功能的影响知之甚少。因此,我们旨在确定体外 IL-6 是否影响破骨细胞的机械敏感性,以及破骨细胞对破骨细胞生成和成骨细胞分化的调节作用。将 MLO-Y4 破骨细胞与/或 IL-6(1 或 10 pg/mL)孵育 24 小时。随后,通过脉动液流(PFF)使破骨细胞机械加载 1 小时。在 IL-6 处理的破骨细胞上培养小鼠破骨细胞前体 7 天。将来自用/未用 IL-6 处理的破骨细胞的条件培养基添加到 MC3T3-E1 前成骨细胞中 14 天。外源性 IL-6(10 pg/mL)不会改变破骨细胞对 PFF 的反应。PFF 显著增强了破骨细胞的 IL-6 产生。IL-6 增强了破骨细胞的 Rankl 表达,但降低了破骨细胞中的 caspase 3/7 活性,因此不影响破骨细胞刺激的破骨细胞生成。来自 IL-6 处理的破骨细胞的条件培养基降低了成骨细胞中的碱性磷酸酶(ALP)活性和 Runx2 表达,但增加了增殖标志物 Ki67 和骨钙素的表达。我们的结果表明,IL-6 是由受剪切力作用的破骨细胞产生的,并且 IL-6 可能通过调节破骨细胞向成骨细胞的通讯来影响骨量。
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