Designer self-assembling peptide scaffold stimulates pre-osteoblast attachment, spreading and proliferation
- 289 Downloads
A new peptide scaffold was made by mixing pure RADA16 (Ac-RADARADARADARADA-CONH2) and designer peptide RGDA16 (Ac-RADARGDARADARGDA-CONH2) solutions, and investigate any effect on attachment, spreading and proliferation of pre-osteoblast (MC3T3-E1). The peptides, RADA16 and RGDA16, were custom-synthesized. They were solubilized in deionized water at a concentration of 10 mg/ml (1% w/v), the RGDA16 peptide solution was mixed 1:1 with RADA16 solution and a new peptide solution RGDAmix was produced. The RGDAmix and RADA16 solution were directly loaded in 96-well plates and cover slips, and two different peptide scaffolds were formed with the addition of maintenance medium (α-MEM) in several minutes. About 1.0 × 104 MC3T3-E1 cells were seeded on each hydrogel scaffold, and then the cell morphological changes were observed using a fluorescence microscope at 1 h, 3 h and 24 h timepoint, respectively. Cell attachment was evaluated 1 h, 3 h and 24 h after cell seeding and cell proliferation was determined 4d, 7d and 14d after cell seeding. The RGDAmix scaffold significantly promoted the initial cell attachment compared with the RADA16 scaffold. MC3T3-E1 cells adhered and spread well on both scaffolds, however, cells spread better on the RGDAmix scaffold than on the RADA16 scaffold. Cell proliferation was greatly stimulated when cultured on RGDAmix scaffold. The RGD sequence contained peptide scaffold RGDAmix significantly enhances MC3T3-E1 cells attachment, spreading and proliferation.
KeywordsCell Attachment Hydrogel Scaffold Footprint Area Nanofiber Scaffold Promote Cell Attachment
This work was sponsored by Zhejiang Provincial Program for the Cultivation of High-level Innovative Health Talents. And supported by Grant of Health Bureau of Zhejiang Province (WKJ 2007-2-015) and Grant of Science and Technology Department of Zhejiang Province (2007C 23016), China.
- 18.A. Rezania, C.H. Thomas, A.B. Branger, C.M. Waters, K.E. Healy, J. Biomed. Mater. Res. 37, 9 (1997). doi: 10.1002/(SICI)1097-4636(199710)37:1<9::AID-JBM2>3.0.CO;2-W PubMedCrossRefGoogle Scholar