Correlation of proliferation, morphology and biological responses of fibroblasts on LDPE with different surface wettability

In order to find a correlation between cell adhesion, growth and biological response with different wettability, NIH/3T3 fibroblast cells were cultured on plasma-treated low-density polyethylene (LDPE) film generated with radio frequency. Different surface wettabilities (water contact angle 90–40°) were created by varying the duration of plasma treatment between 0 and 15 s, respectively. Growth and proliferation rate of cells on LDPE surfaces was evaluated by MTT assay, and cell morphology, by means of spreading and adhesion, was characterized by scanning electron microscopy (SEM). The expression of particular genes in cells contacted on films with different wettability was analyzed by RT-PCR. Using the MTT assay, we confirmed that the amount of cell adhesion was higher on surface of film with a water contact angle of 60° than with other water contact angle. Also, the proliferation rate of cells was highest with a water contact angle of 60°. It was confirmed by SEM that the morphology of cells adhered with a water contact angle of 50–60° was more flattened and activated than on other surfaces. Furthermore, c-fos mRNA in cells showed maximum expression on the film with contact angle range of 50–60° and c-myc mRNA expressed highly on the film with a contact angle of 50°. Finally, p53 gene expression increased as wettability increase. These results indicate that a water contact angle of the polymer surfaces of 50–60° was suitable for cell adhesion and growth, as well as biological responses, and the surface properties play an important role for the morphology of adhesion, growth and differentiation of cells.

[1]  C. Harris,et al.  Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesis. , 1994, Cancer research.

[2]  G. Wogan,et al.  Nitric oxide as a modulator of apoptosis. , 2005, Cancer letters.

[3]  J. Winkles,et al.  Serum- and polypeptide growth factor-inducible gene expression in mouse fibroblasts. , 1998, Progress in nucleic acid research and molecular biology.

[4]  Y. Lee,et al.  Interaction of human chondrocytes and NIH/3T3 fibroblasts on chloric acid-treated biodegradable polymer surfaces , 2002, Journal of biomaterials science. Polymer edition.

[5]  M. Akashi,et al.  Evaluation of biological responses to polymeric biomaterials by RT-PCR analysis III: study of HSP 70, 90 and 47 mRNA expression. , 1998, Biomaterials.

[6]  Z. Rzaev,et al.  Plasma surface modification of polyethylene with organosilicon and organotin monomers , 1996 .

[7]  M. Akashi,et al.  Evaluation of biological responses to polymeric biomaterials by RT-PCR analysis IV: study of c-myc, c-fos and p53 mRNA expression. , 2000, Biomaterials.

[8]  C. M. Alves,et al.  Modulating bone cells response onto starch-based biomaterials by surface plasma treatment and protein adsorption. , 2007, Biomaterials.

[9]  Lee,et al.  The Effect of Fluid Shear Stress on Endothelial Cell Adhesiveness to Polymer Surfaces with Wettability Gradient. , 2000, Journal of colloid and interface science.

[10]  Donald L. Wise,et al.  Encyclopedic Handbook of Biomaterials and Bioengineering , 1995 .

[11]  Sang Jin Lee,et al.  The effect of surface wettability on induction and growth of neurites from the PC-12 cell on a polymer surface. , 2003, Journal of colloid and interface science.

[12]  A F von Recum,et al.  Quantitative analysis of fibroblast morphology on microgrooved surfaces with various groove and ridge dimensions. , 1996, Biomaterials.