Ramamurthi Anand, Vesely Ivan
Department of Biomedical Engineering, ND20, Lerner Research Institute, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio 44120, USA.
J Biomed Mater Res A. 2003 Aug 1;66(2):317-29. doi: 10.1002/jbm.a.10588.
Hyaluronan (HA) gels (hylans) crosslinked with divinyl sulfone (DVS) are highly biocompatible and can be structurally modified to obtain desired mechanical properties that are attractive for their use as tissue-engineering scaffolds. However, unmodified hylan gels are not good substrates for cell attachment or infiltration, likely as a result of their smooth surface and the highly anionic nature of HA. This study investigated whether the cell-adhering characteristics of hylan gels could be enhanced by irradiation with ultraviolet (UV) light, with or without prior dehydration. The attachment and proliferation of neonatal rat smooth muscle cells atop these gels was compared with that on unmodified (control; C) or dehydrated (D) gels. UV-induced changes to gel structure and chemistry were characterized by confocal and electron microscopy, and fluorphore-assisted carbohydrate electrophoresis (FACE). Cell attachment was sparse on both unmodified (C) and dehydrated (D) gels. Significantly higher levels of cell attachment were observed on the surface of irradiated (UV) and dehydrated-irradiated (DUV) gels, likely because of texturing of the gel surface by UV light. In addition, dehydration of gels before UV irradiation created irregular pore-like structures through which cells appeared to migrate into the interior. FACE assays demonstrated that UV-irradiation alters the chemistry of HA, causing limited breakdown of HA chains and DVS crosslinks within gel and possibly creating new crosslinks that have not yet been identified. Because the hylan gels are altered structurally and chemically, binding of cells to the material is likely to be more permanent than possible by other approaches, such as coating of cell-adhesive matrix factors on the gel surface, described previously. The significance of this work is that we have developed a technique for the modification of DVS-crosslinked HA (hylans) to enhance their performance as a cellular scaffold for tissue-engineering applications.
与二乙烯砜(DVS)交联的透明质酸(HA)凝胶(hylans)具有高度生物相容性,并且可以进行结构修饰以获得所需的机械性能,这使其作为组织工程支架具有吸引力。然而,未修饰的hylan凝胶不是细胞附着或浸润的良好底物,这可能是由于其光滑的表面和HA的高阴离子性质所致。本研究调查了hylan凝胶的细胞粘附特性是否可以通过紫外线(UV)照射来增强,无论是否预先脱水。将新生大鼠平滑肌细胞在这些凝胶上的附着和增殖与未修饰(对照;C)或脱水(D)凝胶上的情况进行了比较。通过共聚焦显微镜、电子显微镜和荧光辅助碳水化合物电泳(FACE)对UV诱导的凝胶结构和化学变化进行了表征。在未修饰(C)和脱水(D)凝胶上细胞附着都很稀疏。在照射(UV)和脱水照射(DUV)凝胶表面观察到明显更高水平的细胞附着,这可能是由于UV光使凝胶表面形成纹理所致。此外,在UV照射前对凝胶进行脱水会产生不规则的孔状结构,细胞似乎通过这些结构迁移到内部。FACE分析表明,UV照射会改变HA的化学性质,导致凝胶内HA链和DVS交联的有限分解,并可能形成尚未确定的新交联。由于hylan凝胶在结构和化学上发生了改变,细胞与材料的结合可能比其他方法(如先前所述的在凝胶表面包被细胞粘附基质因子)更持久。这项工作的意义在于,我们开发了一种修饰DVS交联HA(hylans)的技术,以提高其作为组织工程应用细胞支架的性能。