Department of Biomedical Engineering, Sackler School of Biomedical Science, Tufts University, 4 Colby St., Medford, Massachusetts 02155, USA.
Macromol Biosci. 2010 Jun 11;10(6):664-73. doi: 10.1002/mabi.200900452.
Transparent, biodegradable, mechanically robust, and surface-patterned silk films were evaluated for the effect of surface morphology on human corneal fibroblast (hCF) cell proliferation, orientation, and ECM deposition and alignment. A series of dimensionally different surface groove patterns were prepared from optically graded glass substrates followed by casting poly(dimethylsiloxane) (PDMS) replica molds. The features on the patterned silk films showed an array of asymmetric triangles and displayed 37-342 nm depths and 445-3 582 nm widths. hCF DNA content on all patterned films were not significantly different from that on flat silk films after 4 d in culture. However, the depth and width of the grooves influenced cell alignment, while the depth differences affected cell orientation; overall, deeper and narrower grooves induced more hCF orientation. Over 14 d in culture, cell layers and actin filament organization demonstrated that confluent hCFs and their cytoskeletal filaments were oriented along the direction of the silk film patterned groove axis. Collagen type V and proteoglycans (decorin and biglycan), important markers of corneal stromal tissue, were highly expressed with alignment. Understanding corneal stromal fibroblast responses to surface features on a protein-based biomaterial applicable in vivo for corneal repair potential suggests options to improve corneal tissue mimics. Further, the approaches provide fundamental biomaterial designs useful for bioengineering oriented tissue layers, an endemic feature in most biological tissue structures that lead to critical tissue functions.
我们评估了透明、可生物降解、机械强度高且表面图案化的丝素膜对人角膜成纤维细胞(hCF)增殖、取向、细胞外基质(ECM)沉积和排列的表面形貌的影响。首先,从光学级玻璃衬底制备一系列具有不同尺寸的表面槽图案,然后浇铸聚二甲基硅氧烷(PDMS)复制品模具。图案化丝素膜上的特征显示出一系列不对称三角形,深度为 37-342nm,宽度为 445-3582nm。在培养 4 天后,所有图案化薄膜上的 hCF DNA 含量与丝素薄膜上的 DNA 含量没有显著差异。然而,槽的深度和宽度影响细胞排列,而深度差异影响细胞取向;总体而言,较深和较窄的槽诱导更多的 hCF 取向。在培养 14 天以上时,细胞层和肌动蛋白丝组织显示出,细胞层和细胞骨架丝沿着丝素膜图案化槽轴的方向排列。角膜基质组织的重要标志物胶原蛋白 V 和蛋白聚糖(decorin 和 biglycan)高度表达且排列整齐。了解角膜基质成纤维细胞对可用于体内角膜修复的基于蛋白质的生物材料表面特征的反应,为改善角膜组织模拟物提供了选择。此外,这些方法为生物工程定向组织层提供了基本的生物材料设计,这是大多数生物组织结构的固有特征,可导致关键的组织功能。