Fischell Department of Bioengineering, University of Maryland, 3121 A. James Clark Hall, College Park, MD 20742, United States; Center for Engineering Complex Tissues, University of Maryland, 3121 A. James Clark Hall, College Park, MD 20742, United States.
Fischell Department of Bioengineering, University of Maryland, 3121 A. James Clark Hall, College Park, MD 20742, United States; Center for Engineering Complex Tissues, University of Maryland, 3121 A. James Clark Hall, College Park, MD 20742, United States.
Acta Biomater. 2019 Jan 1;83:177-188. doi: 10.1016/j.actbio.2018.10.025. Epub 2018 Oct 18.
The layers in skin determine its protective and hemostasis functions. This layered microstructure cannot be naturally regenerated after severe burns; we aim to reconstruct it using guided tissue regeneration (GTR). In GTR, a membrane is used to regulate tissue growth by stopping fast-proliferating cells and allowing slower cells to migrate and reconstruct specialized microstructures. Here, we proposed the use of keratin membranes crosslinked via dityrosine bonding. Variables from the crosslinking process were grouped within an energy density (ED) parameter to manufacture and evaluate the membranes. Sol fraction, spectrographs, and thermograms were used to quantify the non-linear relation between ED and the resulting crosslinking degree (CD). Mechanical and swelling properties increased until an ED threshold was reached; at higher ED, the CD and properties of the membranes remained invariable indicating that all possible dityrosine bonds were formed. Transport assays showed that the membranes allow molecular diffusion; low ED membranes retain solutes within their structure while the high ED samples allow higher transport rates indicating that uncrosslinked proteins can be responsible of reducing transport. This was confirmed with lower transport of adipogenic growth factors to stem cells when using low ED membranes; high ED samples resulted in increased production of intracellular lipids. Overall, we can engineer keratin membranes with specific CD, a valuable tool to tune microstructural and transport properties.
皮肤的分层结构决定了其保护和止血功能。严重烧伤后,这种分层的微观结构无法自然再生;我们旨在使用引导组织再生(GTR)来重建它。在 GTR 中,使用膜通过阻止快速增殖的细胞并允许较慢的细胞迁移和重建专门的微观结构来调节组织生长。在这里,我们提出使用通过二酪氨酸键交联的角蛋白膜。交联过程中的变量被分组到能量密度(ED)参数内,以制造和评估膜。采用溶度分数、光谱图和热图谱来定量 ED 和由此产生的交联度(CD)之间的非线性关系。力学性能和溶胀性能增加,直到达到 ED 阈值;在更高的 ED 下,CD 和膜的性能保持不变,表明形成了所有可能的二酪氨酸键。转运实验表明,膜允许分子扩散;低 ED 膜将溶质保留在其结构内,而高 ED 样品允许更高的转运速率,表明未交联的蛋白质可能是降低转运的原因。当使用低 ED 膜时,向干细胞转运脂肪生成生长因子的转运减少证实了这一点;高 ED 样品导致细胞内脂质产量增加。总的来说,我们可以用特定的 CD 来设计角蛋白膜,这是一种调节微观结构和转运性能的有价值的工具。