Yoo Han-Seok, Chung Kang-Hyun, Lee Kwon-Jai, Kim Dong-Hee, An Jeung Hee
Department of Food Science and Technology, Seoul National University of Science & Technology, Seoul 01811, Korea.
Department of Advanced Materials Engineering, Daejeon University, Daejeon 34520, Korea.
Nutr Res Pract. 2017 Jun;11(3):190-197. doi: 10.4162/nrp.2017.11.3.190. Epub 2017 Mar 10.
BACKGROUND/OBJECTIVES: (GD) is a natural mutant breed of chicken in Korea with an atypical characterization of melanin in its tissue. This study investigated the effects of melanin extracts of GD on osteoblast differentiation and inhibition of osteoclast formation.
MATERIALS/METHODS: The effects of the melanin extract of GD on human osteoblast MG-63 cell differentiation were examined by evaluating cell viability, osteoblast differentiation, and expression of osteoblast-specific transcription factors such as bone morphogenetic protein 2 (BMP-2), small mothers against decapentaplegic homologs 5 (SMAD5), runt-related transcription factor 2 (RUNX2), osteocalcin and type 1 collagen (COL-1) by reverse transcription-polymerase chain reaction and western blotting analysis. We investigated the inhibitory effect of melanin on the osteoclasts formation through tartrate-resistant acid phosphatase (TRAP) activity and TRAP stains in Raw 264.7 cell.
The melanin extract of GD was not cytotoxic to MG-63 cells at concentrations of 50-250 µg/mL. Alkaline phosphatase (ALP) activity and bone mineralization of melanin extract-treated cells increased in a dose-dependent manner from 50 to 250 µg/mL and were 149% and 129% at 250 µg/mL concentration, respectively ( < 0.05). The levels of BMP-2, osteocalcin, and COL-1 gene expression were significantly upregulated by 1.72-, 4.44-, and 2.12-fold in melanin-treated cells than in the control cells ( < 0.05). The levels of RUNX2 and SMAD5 proteins were higher in melanin-treated cells than in control vehicle-treated cells. The melanin extract attenuated the formation of receptor activator of nuclear factor kappa-B ligand-induced TRAP-positive multinucleated RAW 264.7 cells by 22%, and was 77% cytotoxic to RAW 264.7 macrophages at a concentration of 500 µg/mL.
This study provides evidence that the melanin extract promoted osteoblast differentiation by activating BMP/SMADs/RUNX2 signaling and regulating transcription of osteogenic genes such as ALP, type I collagen, and osteocalcin. These results suggest that the effective osteoblastic differentiation induced by melanin extract from GD makes it potentially useful in maintaining bone health.
背景/目的:(GD)鸡是韩国的一种天然突变品种,其组织中黑色素具有非典型特征。本研究调查了GD黑色素提取物对成骨细胞分化和破骨细胞形成抑制的影响。
材料/方法:通过评估细胞活力、成骨细胞分化以及成骨细胞特异性转录因子如骨形态发生蛋白2(BMP-2)、小抗五聚体蛋白同源物5(SMAD5)、 runt相关转录因子2(RUNX2)、骨钙素和I型胶原蛋白(COL-1)的表达,采用逆转录-聚合酶链反应和蛋白质印迹分析,检测GD黑色素提取物对人成骨细胞MG-63细胞分化的影响。我们通过抗酒石酸酸性磷酸酶(TRAP)活性和TRAP染色,研究了黑色素对Raw 264.7细胞中破骨细胞形成的抑制作用。
GD黑色素提取物在浓度为50 - 250μg/mL时对MG-63细胞无细胞毒性。黑色素提取物处理的细胞碱性磷酸酶(ALP)活性和骨矿化从50到250μg/mL呈剂量依赖性增加, 在250μg/mL浓度时分别为149%和129%(P<0.05), 黑色素处理的细胞中BMP-2、骨钙素和COL-1基因表达水平分别比对照细胞显著上调1.72倍、4.44倍和2.12倍(P<0.05)。黑色素处理的细胞中RUNX2和SMAD5蛋白水平高于对照载体处理的细胞。黑色素提取物使核因子κB受体激活剂配体诱导的TRAP阳性多核RAW 264.7细胞的形成减少了22%,在浓度为500μg/mL时对RAW 264.7巨噬细胞的细胞毒性为77%。
本研究提供了证据表明,黑色素提取物通过激活BMP/SMADs/RUNX2信号通路和调节成骨基因如ALP、I型胶原蛋白和骨钙素的转录来促进成骨细胞分化。这些结果表明,GD黑色素提取物诱导的有效成骨细胞分化使其在维持骨骼健康方面具有潜在用途。