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Article type: Research Article
Authors: Yao, W.J. | Liang, Y. | Chen, K. | Xie, L.D. | Sun, D.G. | Wang, X.J. | Wen, Z.Y.; | Chien, S.
Affiliations: Hemorheology Center, Department of Biophysics, School of Basic Medical Sciences, Peking University, Beijing, 100083, P.R. China | Department of Biochemical and Molecular Biology, School of Basic Medical Sciences, Peking University, Beijing, 100083, P.R. China | Department of Bioengineering and Whitaker Institute of Biomedical Engineering, University of California, San Diego, La Jolla, CA 92093‐0412, USA
Note: [] Corresponding author: Wen Zong‐Yao, Hemorheology center, Department of Biophysics, School of Basic Medical Sciences, Peking University, Beijing, 100083, P.R. China. Tel.: 86 10 620 92419; Fax: 86 10 620 15582; E‐mail: [email protected].
Abstract: p16 gene was transferred into human erythroleukemia cell line K562 that had been subjected to p16 deletion. The changes of biophysical behavior of K562 cells after gene transfer were studied with the micropipette technique. The micropipette data were analyzed with a standard solid viscoelastic model. In comparison to untransfected control K562 cells and the cells transfected with an empty vector, the p16‐transfected K562 cells showed an increase in the elastic element K1, which is inversely proportional to the maximum deformation over a long period of time, whereas the viscous element μ and the other elastic element K2 showed no significant difference. The results indicate that K562 cells became more rigid after p16 transfer. The p16‐transfected K562 cells also had a higher surface charge density. This study contributes to our knowledge about the suppression effect of p16 gene on tumor cell migration and about its use in gene therapy.
Keywords: K562 cells, p16 gene, micropipette, viscoelasticity
Journal: Clinical Hemorheology and Microcirculation, vol. 27, no. 3-4, pp. 177-183, 2002
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