University of Grenoble 1/CNRS, LIPhy UMR 5588, BP 87, 38041 Grenoble, France.
Langmuir. 2012 Dec 4;28(48):16623-37. doi: 10.1021/la303443t. Epub 2012 Nov 20.
Thermoresponsive tissue culture substrates based on PNIPAM brushes are used to harvest confluent cell sheets for tissue engineering. The prospect of clinical use imposes the utilization of culture medium free of bovine serum, thus suggesting conjugation with adhesion peptides containing the RGD minimal recognition sequence. The optimum position of the RGD along the chain should ensure both cell adhesion at 37 °C and cell detachment at T(L) below the lower critical solution temperature of PNIPAM. Design guidelines are formulated from considerations of brush confinement by the cells: (i) Cell adhesion at 37 °C is controlled by the RGDs accessible without brush compression. (ii) Cell detachment at T(L) is driven by a disjoining force due to confinement of the swollen brush by cells retaining integrin-RGD bonds formed at 37 °C. These suggest placing the RGDs at the grafting surface or its vicinity. Randomly placed RGDs do not enable efficient detachment because a large fraction of the integrin-RGD bonds are not sufficiently tensioned at T(L), in line with experimental observations (Ebara, M.; Yamato, M.; Aoyagi, T.; Kikuchi, A.; Sakai, K.; Okano, T. Immobilization of celladhesive peptides to temperature-responsive surfaces facilitates both serum-free cell adhesion and noninvasive cell harvest. Tissue Eng. 2004, 10, 1125-1135). The theory framework enables analysis of culture media based on polymer brushes conjugated with adhesion peptides in general.
基于 PNIPAM 刷的温敏组织培养基质用于收获细胞片用于组织工程。临床应用的前景要求使用不含牛血清的培养基,因此建议与含有 RGD 最小识别序列的粘附肽缀合。沿链的 RGD 的最佳位置应确保在 37°C 时细胞粘附和低于 PNIPAM 下临界溶液温度的 T(L)时细胞脱落。设计准则是从细胞对刷的限制的考虑中得出的:(i)在 37°C 时的细胞粘附受无刷压缩时可及的 RGD 控制。(ii)在 T(L)时的细胞脱落是由膨胀刷由于细胞保留在 37°C 时形成的整合素-RGD 键的限制而产生的离解力驱动的。这表明将 RGD 放置在接枝表面或其附近。随机放置的 RGD 不能实现有效的脱落,因为在 T(L)时,很大一部分整合素-RGD 键没有充分拉紧,这与实验观察结果一致(Ebara,M.;Yamato,M.;Aoyagi,T.;Kikuchi,A.;Sakai,K.;Okano,T. 将细胞粘附肽固定在温度响应表面上有助于无血清细胞粘附和非侵入性细胞收获。组织工程。2004 年,10,1125-1135)。该理论框架能够分析一般与粘附肽缀合的聚合物刷的培养基。