Kushida A, Yamato M, Konno C, Kikuchi A, Sakurai Y, Okano T
Institute of Biomedical Engineering, Tokyo Women's Medical University, Japan.
J Biomed Mater Res. 1999 Jun 15;45(4):355-62. doi: 10.1002/(sici)1097-4636(19990615)45:4<355::aid-jbm10>3.0.co;2-7.
Bovine aortic endothelial cells were cultured on surfaces grafted with a temperature-responsive polymer, poly(N-isopropylacrylamide) (PIPAAm), in the presence of serum. Cells adhered, spread, proliferated, and reached confluency as observed on ungrafted tissue culture polystyrene dishes. A decrease in culture temperature released cells only from the grafted surfaces without enzymatic or ethylenediaminetetraacetic acid treatment. Upon lowering temperature, the culture surfaces changed from hydrophobic to hydrophilic owing to the hydration of grafted PIPAAm and thus weakened the cell attachment to the dishes. Released cells maintained cell-cell junctions composing monolayer cell sheets. Immunoblotting and immunofluorescence microscopy revealed that fibronectin (FN) was deposited and accumulated on the grafted surfaces during the culture. Furthermore, the deposited FN matrix adhering to cell sheets was also recovered from temperature-responsive surfaces by low-temperature treatment, while trypsin treatment destroyed the matrix. The recovery of FN by low-temperature treatment was as high as by physical scraping with a rubber blade. Temperature-responsive surfaces can provide a novel method to use cultured confluent cell sheets for tissue engineering, and also to elucidate structure and function of deposited extracellular matrix during cell culture.
在有血清存在的情况下,将牛主动脉内皮细胞培养在接枝有温度响应性聚合物聚(N-异丙基丙烯酰胺)(PIPAAm)的表面上。细胞能够黏附、铺展、增殖并达到汇合状态,这与在未接枝的组织培养聚苯乙烯培养皿上观察到的情况相同。降低培养温度可使细胞仅从接枝表面脱离,而无需酶处理或乙二胺四乙酸处理。降温时,由于接枝的PIPAAm发生水合作用,培养表面从疏水变为亲水,从而削弱了细胞与培养皿的附着。脱离的细胞保持组成单层细胞片的细胞间连接。免疫印迹和免疫荧光显微镜检查显示,在培养过程中纤连蛋白(FN)沉积并积聚在接枝表面。此外,通过低温处理也可从温度响应表面回收附着在细胞片上的沉积FN基质,而胰蛋白酶处理会破坏该基质。低温处理回收FN的效率与用橡胶刮刀物理刮擦的效率一样高。温度响应表面可为组织工程中使用培养的汇合细胞片提供一种新方法,同时也有助于阐明细胞培养过程中沉积的细胞外基质的结构和功能。