Niepel Marcus S, Peschel Dieter, Sisquella Xavier, Planell Josep A, Groth Thomas
Biomedical Materials Group, Department of Pharmaceutical Technology and Biopharmacy, Institute of Pharmacy, Martin Luther University Halle-Wittenberg, D-06099 Halle (Saale), Germany.
Biomaterials. 2009 Oct;30(28):4939-47. doi: 10.1016/j.biomaterials.2009.06.014. Epub 2009 Jul 1.
Adhesion of tissue cells is a prerequisite for their growth and differentiation but prevents also apoptosis. Here the layer-by-layer technique (LbL) was used to design multilayer structures of poly(ethylene imine) (PEI) and heparin (HEP) on glass as model biomaterial to control the adhesion of primary human dermal fibroblasts. Distinct surface features like wettability, charge and lateral structures were controlled by changing the pH value of the HEP solution during multilayer assembly to acidic, neutral or alkaline values. While plain terminal layers were rather cytophobic, the pre-adsorption of serum or fibronectin (FN) caused a distinct change in cell morphology in dependence on the pH setup. The effect of serum was more prominent on PEI layers probably due to their positive surface charge, whereas the effect of FN was more pronounced on HEP terminated multilayers possibly due to its ability to bind FN specifically. Those layers which hampered cell adhesion also inhibited growth of human fibroblasts under serum conditions. Conversely, on layers where cell adhesion was increased also an elevated growth and, thus, metabolic activity was observed.
组织细胞的黏附是其生长和分化的先决条件,但也能防止细胞凋亡。在此,采用层层组装技术(LbL)在玻璃上设计聚(乙烯亚胺)(PEI)和肝素(HEP)的多层结构作为模型生物材料,以控制原代人皮肤成纤维细胞的黏附。在多层组装过程中,通过将HEP溶液的pH值改变为酸性、中性或碱性值,来控制诸如润湿性、电荷和横向结构等不同的表面特征。虽然普通的终端层具有较强的疏细胞性,但血清或纤连蛋白(FN)的预吸附会根据pH设置导致细胞形态发生明显变化。血清对PEI层的影响可能更为显著,这可能是由于其表面带正电荷,而FN对HEP终端多层结构的影响可能更为明显,这可能是由于其特异性结合FN的能力。那些阻碍细胞黏附的层在血清条件下也会抑制人成纤维细胞的生长。相反,在细胞黏附增加的层上,也观察到生长增加,进而代谢活性升高。