|
|
Effect of Regesi regeneration silicon and Bio-Oss bone meal on proliferation and osteogenic differentiation of osteoblasts |
JIA Yan1 ZHANG Baorong2 |
1.Oral Medicine School, Weifang Medical College, Shandong Province, Weifang 261053, China;
2.Oral Clinic, Aviation General Hospital, Beijing 100012, China |
|
|
Abstract Objective To observe the growth of mouse osteoblast (MC3T3-E1) on Regesi regeneration silicon and Bio-Oss bone powder, and to analyze the effects of Regesi regeneration silicon materials and Bio-Oss bone powder on mouse osteoblast proliferation and osteogenic differentiation. Methods The experiment was divided into three groups, respectively Regesi regeneration silicon group, Bio-Oss bone powder group and control group. The two materials were placed in 24-well plates, while the control group was blank. Cells were inoculated on 24-well plates in each group, and the cell growth was observed by inverted microscope at 1, 4 days, and 7 days of culture; MTT was used to detect cell proliferation activity at 1, 4 days, and 7 days of culture; OD value of osteoblasts was determined by alkaline phosphatase (ALP) kit at 7 d culture to analyze ALP activity. Rt-PCR method was used to determine Runx2 and Osterix(OSX) gene expression in 3 groups of cells at 7 days of culture. Results Under the microscope, the number of cells in each group increased with time. The proliferation level of cells in Regesi group increased (P < 0.05), and the ALP activity elevated,the expression levels of Runx2 and OSX mRNA increased at 7 days of culture(P < 0.05). The proliferation level of cells in the bio-Oss bone meal group was decreased at 7 days of culture(P < 0.05), and there was no significant difference in the ALP activity, and the expression levels of Runx2 and OSX mRNA (P > 0.05). Conclusion Regesi regenerated silicon can promote the proliferation and differentiation of MC3T3-E1 cells. Bio-Oss bone powder can decrease cell proliferation, while there is no significant difference between osteogenic differentiation ability and osteoblasts alone.
|
|
|
|
|
[1] He B,Yuan X,Wu J,et al. Self-Assembling peptide nanofiber scaffolds for bone tissue engineering [J]. S Advanced Mater,2015,7(7):1221-1232.
[2] 章筛林,成翔宇,纪斌.硅在生物材料领域的应用:增加材料生物活性不影响其机械性能[J].中国组织工程研究,2017,21(2):296-302.
[3] 强巴单增,刘晓兰.多孔纳米羟基磷灰石/聚酰胺复合骨修复材料的制备[J].中国组织工程研究,2016,20(3):392-396.
[4] 廖建国,李艳群,段星泽,等.纳米羟基磷灰石/聚合物复合骨修复材料[J].化学进展,2015,27(2):220-228.
[5] 陈冬,白轶,李蓉,等.新型骨修复材料修复种植牙骨缺损的前瞻性临床研究[J].口腔医学研究,2015,31(11):1129-1132.
[6] Kaur G,Pickrell G,Sriranganathan N,et al. Review and the state of the art:Sol-gel and melt quenched bioactive glasses for tissue engineering [J]. J Biomed Mater Res B Appl Biomater,2016,104(6):1248-1275.
[7] Chen XF,Lei B,Wang YJ,et al. Morphological control and in vitro bioactivity of nanoscale bioactive glasses [J]. J Non-Crystalline Solids,2009,355(13)791-796..
[8] Chen XF,Guo CL,Zhao N. Preparation and characterization of the sol-gel nano-bioactive glasses modified by the coupling agent gamma-aminopropyltriethoxysilane [J]. Applied Surface Science,2008,255(2):491-499.
[9] Zheng MH,Wood DJ,Papadimitriou JM. What′s new in the role of cytokines on osteoblast proliferation and differentiation? [J]. Pathol Res Pract,1992,188(8):1104-1121.
[10] Chung SL,Leung KS,Cheung WH. Low-magnitude high-frequency vibration enhances gene expression related to callus formation,mineralization and remodeling during osteoporotic fracture healing in rats [J]. J Orthop Res,2014,32(12):1572-1579.
[11] 戴永国,蔡立飞,杨洋,等.磷酸肌酸对小鼠前成骨细胞MC3T3-E1增殖、分化及矿化的影响[J].大连医科大学学报,2018,40(4):296-300,306.
[12] 唐林,林珠,李永明,等.不同大小机械牵张力对成骨细胞增殖及碱性磷酸酶的影响[J].解放军医学杂志,2006, 31(6):580-581.
[13] 邵华英,张一弓,杨雪,等.抑菌浓度米诺环素对成骨细胞增殖、分化和矿化的影响[J].华西口腔医学杂志,2018, 36(2):140-145.
[14] Kumar Y,Kapoor I,Khan K,et al. E3 Ubiquitin Ligase Fbw7 Negatively Regulates Osteoblast Differentiation by Targeting Runx2 for Degradation [J]. J Biolo Chem,2015, 290(52):471-474.
[15] Bruderer M,Richards RG,Alini M,et al. Role and regulation of RUNX2 in osteogenesis [J]. Eur Cells Mater,2014,28(28):269-286.
[16] Nakashima K,Zhou X,Kunkel G,et al. The novel zinc finger-containing transcription factor osterix is required for ostcoblast differentiation and bone formation [J]. Cell,2002,108(1):17-29.
[17] Sinha KM,Zhou X. Genetic and molecular control of osterix in skeletal formation [J]. J Cell Biochem,2013(5):975-984.
[18] 杨丹,于燕妮.成骨细胞特异性转录因子Osterix研究进展[J].中国公共卫生,2013,29(1):142-145.
[19] Ste in GS,Lian JB,van Wijnen AJ,et al. Runx2 control of organization,assembly and activity of the regulatory machinery for skeletal gene expression [J]. Oncogene,2004,23(24):4315-4329.
[20] Zhang C. Transcriptional regulation of bone formation by the osteoblast-specific transcription factor Osx [J]. J Orthop Surg Res,2010,5(1):37. |
|
|
|