Jeong Jin-Woo, Ji Seon Yeong, Lee Hyesook, Hong Su Hyun, Kim Gi-Young, Park Cheol, Lee Bae-Jin, Park Eui Kyun, Hyun Jin Won, Jeon You-Jin, Choi Yung Hyun
Nakdonggang National Institute of Biological Resources, Sangju 37242, Korea.
Department of Biochemistry, Dong-eui University College of Korean Medicine, Busan 47227, Korea.
Foods. 2019 Jul 26;8(8):290. doi: 10.3390/foods8080290.
Sea tangle ( 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.
海带(墨角藻属),一种褐藻,多年来一直被用作亚太地区的功能性食品成分。在本研究中,我们使用RAW 264.7小鼠巨噬细胞,研究了发酵海带提取物(FST)对核因子κB(NF-κB)配体(RANKL)刺激的破骨细胞分化的影响。发现FST可抑制RANKL刺激的抗酒石酸酸性磷酸酶(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激活和活化T细胞核因子c1(NFATc1)(一种主要转录因子)的表达,下调了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。此外,FST通过激活核因子红系2相关因子2(Nrf2)及其转录靶点,显著消除了RANKL诱导的活性氧(ROS)生成。因此,FST可能因其能够使NF-κB介导的NFATc1信号通路失活,并通过激活Nrf2途径减少ROS产生而具有抗破骨细胞生成的潜力。尽管需要进一步研究以探究其体内疗效,但FST似乎有潜力用作破骨性骨病的辅助治疗或预防性治疗。