首页> 美国卫生研究院文献>Foods >Fermented Sea Tangle (Laminaria japonica Aresch) Suppresses RANKL-Induced Osteoclastogenesis by Scavenging ROS in RAW 264.7 Cells
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Fermented Sea Tangle (Laminaria japonica Aresch) Suppresses RANKL-Induced Osteoclastogenesis by Scavenging ROS in RAW 264.7 Cells

机译:发酵海纠结(海带)清除RAW 264.7细胞中的ROS抑制RANKL诱导的破骨细胞生成。

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摘要

Sea tangle (Laminaria japonica Aresch), a brown alga, has been used for many years as a functional food ingredient in the Asia-Pacific region. In the present study, we investigated the effects of fermented sea tangle extract (FST) on receptor activator of nuclear factor-κB (NF-κB) ligand (RANKL)-stimulated osteoclast differentiation, using RAW 264.7 mouse macrophage cells. FST was found to inhibit the RANKL-stimulated activation of tartrate-resistance acid phosphatase (TRAP) and F-actin ring structure formation. FST also down-regulated the expression of osteoclast marker genes like TRAP, matrix metalloproteinase-9, cathepsin K and osteoclast-associated receptor by blocking RANKL-induced activation of NF-κB and expression of nuclear factor of activated T cells c1 (NFATc1), a master transcription factor. In addition, FST significantly abolished RANKL-induced generation of reactive oxygen species (ROS) by activation of nuclear factor-erythroid 2-related factor 2 (Nrf2) and its transcriptional targets. Hence, it seems likely that FST may have anti-osteoclastogenic potential as a result of its ability to inactivate the NF-κB-mediated NFATc1 signaling pathway and by reducing ROS production through activation of the Nrf2 pathway. Although further studies are needed to inquire its efficacy in vivo, FST appears to have potential use as an adjunctive or as a prophylactic treatment for osteoclastic bone disease.
机译:海藻(Laminaria japonica Aresch)是一种棕色藻类,在亚太地区已被用作功能性食品成分多年。在本研究中,我们使用RAW 264.7小鼠巨噬细胞研究了发酵的海纠缠提取物(FST)对核因子-κB(NF-κB)配体(RANKL)刺激的破骨细胞分化受体激活剂的影响。发现FST抑制RANKL刺激的酒石酸抗性酸性磷酸酶(TRAP)的激活和F-肌动蛋白环结构的形成。 FST还通过阻断RANKL诱导的NF-κB活化和活化T细胞c1(NFATc1)的核因子表达来下调破骨细胞标记基因(如TRAP,基质金属蛋白酶9,组织蛋白酶K和破骨细胞相关受体)的表达,主转录因子。此外,FST通过激活核因子-类胡萝卜素2相关因子2(Nrf2)及其转录靶标,显着消除了RANKL诱导的活性氧(ROS)生成。因此,由于FST能够灭活NF-κB介导的NFATc1信号通路并通过激活Nrf2通路减少ROS产生,因此可能具有抗破骨细胞的潜力。尽管需要进一步的研究以探究其在体内的功效,但FST似乎有可能作为破骨性骨病的辅助治疗或预防性治疗。

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