Kim Hyung Keun, Park Sang Jin, Kim Ji Hyun, Kim Jin, Lee Ki-Young, Yoon Taek Rim
Department of Orthopaedics, Chonnam National University, Hwasun Hospital, 160, Ilsim-Ri, Hwasun-Eup, Hwasun-Gun, Jeonnam 519-809, Korea.
J Nanosci Nanotechnol. 2010 May;10(5):3284-8. doi: 10.1166/jnn.2010.2234.
Long-chain eicosapentaenoic acid (EPA) is found mainly in marine oils, and has wide ranging biological effects. In this study, we evaluated the effect of nanoemulsion-EPA on the osteogenic differentiation of mouse mesenchymal stem cells (D1 cells). D1 cells were cultured in osteogenic differentiation medium (ODM) for 6 days and treated with nanoemulsion-EPA for 2 days and then subjected to various tests; MTT assays, alizarin red S staining, alkaline phosphatase (ALP) activity determinations, calcium contents analysis, reverse transcriptase-polymerase chain reaction (RT-PCR), confocal microscopy, and flow cytometric analysis. D1 cells were found to differentiate into osteoblasts in the presence of osteogenic differentiation medium, as determined by positive alizarin red S staining, increased alkaline phosphatase activity and calcium contents, osteocalcin, osteopontin and Runx2 mRNA expressions, and by positive immunofluorescence staining against CD44 or CD51. Furthermore, osteogenic differentiation was enhanced when cells were treated with nanoemulsion-EPA, as determined by alizarin red S staining, elevated ALP activity, calcium contents and osteocalcin and Runx2 mRNA expression, and immunofluorescence staining and flow cytometric analysis for CD44. Furthermore, pretreatment with p38 inhibitor prior to nanoemulsion-EPA decreased alizarin red S staining and ALP activity. These findings suggest that nanoemulsion-EPA enhances osteogenic differentiation via the p38 pathway when administered to mouse mesenchymal stem cells in osteogenic differentiation medium.
长链二十碳五烯酸(EPA)主要存在于海洋油中,具有广泛的生物学效应。在本研究中,我们评估了纳米乳剂-EPA对小鼠间充质干细胞(D1细胞)成骨分化的影响。D1细胞在成骨分化培养基(ODM)中培养6天,并用纳米乳剂-EPA处理2天,然后进行各种测试;MTT分析、茜素红S染色、碱性磷酸酶(ALP)活性测定、钙含量分析、逆转录聚合酶链反应(RT-PCR)、共聚焦显微镜检查和流式细胞术分析。通过茜素红S染色阳性、碱性磷酸酶活性和钙含量增加、骨钙素、骨桥蛋白和Runx2 mRNA表达以及针对CD44或CD51的免疫荧光染色阳性,发现D1细胞在成骨分化培养基存在下分化为成骨细胞。此外,当用纳米乳剂-EPA处理细胞时,成骨分化增强,这通过茜素红S染色、升高的ALP活性、钙含量以及骨钙素和Runx2 mRNA表达以及CD44的免疫荧光染色和流式细胞术分析来确定。此外,在纳米乳剂-EPA之前用p38抑制剂预处理可降低茜素红S染色和ALP活性。这些发现表明,当在成骨分化培养基中给予小鼠间充质干细胞时,纳米乳剂-EPA通过p38途径增强成骨分化。