Journal of Peking University(Health Sciences) ›› 2018, Vol. 50 ›› Issue (1): 176-182. doi: 10.3969/j.issn.1671-167X.2018.01.030

• Article • Previous Articles     Next Articles

Effects of RGD peptides-grafted porous tantalum on morphological change of MG63 osteoblasts-tantalum conjunctive interface and expression of osteogenesis factors

GAN Hong-quan1, WANG Qian2, ZHANG Hui3, LIU Xin4, DENG Hua-min1, SONG Hui-ping1, WANG ZHi-qiang1, LI Qi-jia5△   

  1. (1. Department of Orthopaedics, Affiliated Hospital, North China University of Science and Technology; 2. Department of Anatomy, Basic Medical College, North China University of Science and Technology; 3. Department of Joint Surgery, the Second Hospital of Tangshan; 4. Department of Clinical Laboratory, Kailuan General Hospital; 5. Experimental Center, North China University of Science and Technology; Tangshan 063000, Hebei, China)
  • Online:2018-02-18 Published:2018-02-18
  • Contact: LI Qi-jia E-mail: qjl1222de@163.com
  • Supported by:
    Supported by the National Ministry of Science and Technology Support Project for “12th Five-Year Plan” (2012BAE06B03), Science and Technology Support Project of Hebei Province (16277776D), Health and Family Planning Commission Clinical Medical Project of Hebei Province (361036), Key Propram for Medical Science Project of Hebei Province (20160225)

Abstract: Objective: To investigate the effects of the Arg-Gly-Asp polypeptedes (RGD) peptides-modified porous tantalum surface on osteoblasts morphology and expressions of osteogenesis factors, and to evaluate RGD peptides promotes junctura ossium of tantalumbone interface in vivo. Methods: RGD peptides of different concentrations (1 g/L, 5 g/L, and 10 g/L) were loaded to porous tantalum slices with a diameter of 10 mm and a thickness of 3 mm by physical absorption. The 3rd generation of MG63 cells were co-cultured with tantalum and divided into 4 groups: Ta-cells (control) group, 1 g/L cells/Ta/RGD group, 5 g/L cells/Ta/RGD group, and 10 g/L cells/Ta/RGD group. Porous tantalum compo-sites and osteoblasts-tantalum interface were observed by scanning electron microscopy. The adhesion rate of osteoblasts was detected and immunocytochemistry was used to detect the expressions of filamentous actin (F-actin), osteocalcin (OC) and fibronectin (FN). Results: The scanning electron microscope (SEM) revealed that osteoblasts distributed on the surface of porous tantalum and secreted extracellular matrix on outside and inner of micro-pores. The osteoblasts adhesion rate on porous tantalum modified with RGD was higher than that in the unmodified porous tantalum at the end of 24, 48, and 72 hours. The best adhesion effect was got in 5 g/L cells/Ta/RGD group at hour 48 [(68.07±3.80) vs. (23.40±4.39), P<0.05]. The results of immunocytochemistry showed that the expressions intensity of F-actin, OC and FN in osteoblasts on porous tantalum modified groups with RGD were stronger than that in the unmodified groups, and the expressions of 5 g/L cells/Ta/RGD group were significantly higher than those in the 10 g/L group and 1 g/L group [OC: (18.08±0.08) vs. (15.14±0.19), P<0.05; (18.08±0.08) vs. (14.04±0.61), P<0.05. FN: (24.60±0.98) vs. (15.90±0.53), P<0.05; (24.60±0.98) vs. (15.30±0.42), P<0.05. Factin: (29.20±1.31) vs. (24.50±1.51), P<0.05; (29.20±1.31) vs. (16.92±0.40), P<0.05]. Correspondingly F-actin in osteoblasts was showed in longitudinal arrangement, and the expressions intensity was stronger than those OC and FN. Conclusion: The RGD peptides is beneficial to enhance adhesion of osteoblast, spreading and reorganization of cytoskeleton on porous tantalum surface and improve the interface morphology, further promoting osteoblasts-tantalum conjunctive interface osseointegration.

Key words: Arg-Gly-Asp polypeptedes peptides, Tantalum, Cell adhesion, Osteoblasts

CLC Number: 

  • R318.08
[1] WANG Zheng,DING Qian,GAO Yuan,MA Quan-quan,ZHANG Lei,GE Xi-yuan,SUN Yu-chun,XIE Qiu-fei. Effect of porous zirconia ceramics on proliferation and differentiation of osteoblasts [J]. Journal of Peking University (Health Sciences), 2022, 54(1): 31-39.
[2] LI Zheng,WANG Xiao,HONG Tian-pei,WANG Hao-jie,GAO Zhan-yi,WAN Meng. Mechanism of advanced glycation end products inhibiting the proliferation of peripheral blood mononuclear cells and osteoblasts in rats [J]. Journal of Peking University (Health Sciences), 2021, 53(2): 355-363.
[3] LING Long, ZHAO Yu-ming, GE Li-hong. Impact of different degree pulpitis on cell proliferation and osteoblastic differentiation of dental pulp stem cell in Beagle immature premolars [J]. Journal of Peking University(Health Sciences), 2016, 48(5): 878-883.
[4] WANG Yi-xiang, AN Na, OUYANG Xiang-ying. Molecular mechanism involved in adhesion of monocytes to endothelial cells induced by nicotine and Porphyromonas gingivalis-LPS [J]. Journal of Peking University(Health Sciences), 2015, 47(5): 809-813.
[5] ZHANG Hui, LI Liang, WANG Qian, GAN Hong-Quan, WANG Hui, BI Cheng, LI Qi-Jia, WANG Zhi-Qiang. Influence of BMP-7 on chondrocyte secretion and expression of Col-Ⅱ,AGG and Sox9 mRNA in porous tantalum-chondrocyte composites in vitro [J]. Journal of Peking University(Health Sciences), 2015, 47(2): 219-225.
[6] ZHONG Jin-Sheng, MEI Fang, ZHANG Hong-Quan. Comparison of biological characteristics of human gingival junctional epithelial cells and oral epithelial cells [J]. Journal of Peking University(Health Sciences), 2015, 47(1): 32-36.
[7] LIU Yan, FU Yu, LIU Shuai, ZHOU Yan-heng. Effects of microstructure of mineralized collagen scaffolds on cell morphology of MG 63 [J]. Journal of Peking University(Health Sciences), 2014, 46(1): 19-24.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!