von Recum A F, van Kooten T G
Department of Bioengineering, Clemson University, SC 29634-0905, USA.
J Biomater Sci Polym Ed. 1995;7(2):181-98. doi: 10.1163/156856295x00698.
Tissue attachment to substratum surfaces is of central importance to the in vivo performance of prosthetic implant materials. It is not yet understood why connective tissue does not attach to the surface of silicone or any other polymeric material. Recently the authors have conclusively demonstrated that micro-range surface roughness modifies cellular responses in cell culture and modifies biocompatibility and tissue attachment in vivo significantly. In order to better understand the basic interactions between living cells or tissues on one hand and man-made substratum surfaces on the other hand, the germane literature is reviewed here. Cells adhere to substratum surfaces mainly through focal adhesions which are a complex of intracellular transmembrane and extracellular proteins. Adhesion is facilitated and modified by proteins adsorbed to the substratum surface. Protein adsorption in turn is modified by the underlying substratum surface properties including surface chemistry, charge, and free energy. When silicone and other polymeric implants having well-defined surface topographic features including pores, pillars, or grooves were implanted, the tissue response to these implants was strongly influenced by the dimensions of these features as well as by other geometric details. Highest biocompatibility along with tissue attachment was seen when topographic features had dimensions of 1-3 microns and a uniform distribution. Cell culture studies revealed that topographic features affect cellular alignment, direction of proliferation, cellular attachment, growth rate, metabolism, and cytoskeletal arrangement. Since discontinuities or curvatures associated with topographic features may represent local changes in surface free energy, it is hypothesized that these discontinuities trigger changes in protein adsorption, protein configuration, and cellular response.
组织与基质表面的附着对于假体植入材料的体内性能至关重要。目前尚不清楚为什么结缔组织不会附着在硅酮或任何其他聚合材料的表面。最近,作者已经确凿地证明,微观尺度的表面粗糙度会改变细胞培养中的细胞反应,并显著改变体内的生物相容性和组织附着。为了更好地理解一方面活细胞或组织与另一方面人造基质表面之间的基本相互作用,在此对相关文献进行综述。细胞主要通过粘着斑附着在基质表面,粘着斑是细胞内跨膜蛋白和细胞外蛋白的复合物。吸附在基质表面的蛋白质促进并改变了粘附作用。反过来,蛋白质吸附又会受到底层基质表面特性的影响,包括表面化学性质、电荷和自由能。当植入具有明确表面形貌特征(包括孔隙、柱状物或凹槽)的硅酮和其他聚合物植入物时,组织对这些植入物的反应受到这些特征的尺寸以及其他几何细节的强烈影响。当地形特征尺寸为1 - 3微米且分布均匀时,观察到最高的生物相容性以及组织附着。细胞培养研究表明,地形特征会影响细胞排列、增殖方向、细胞附着、生长速率、代谢和细胞骨架排列。由于与地形特征相关的不连续性或曲率可能代表表面自由能的局部变化,因此推测这些不连续性会引发蛋白质吸附、蛋白质构象和细胞反应的变化。