Norris Emma G, Majeski Joseph, Wayson Sarah E, Coleman Holly, Choe Regine, Dalecki Diane, Hocking Denise C
Department of Pharmacology and Physiology, University of Rochester, Rochester, New York, 14642, United States of America.
Department of Biomedical Engineering, University of Rochester, Rochester, New York, 14642, United States of America.
Mater Res Express. 2019 Dec;6(12). doi: 10.1088/2053-1591/ab597a. Epub 2019 Nov 29.
Much attention has focused recently on utilizing components of the extracellular matrix (ECM) as natural building blocks for a variety of tissue engineering applications and regenerative medicine therapies. Consequently, new fabrication methods are being sought to enable molecular control over the structural characteristics of ECM molecules in order to improve their biological function. Exposing soluble collagen to acoustic forces associated with ultrasound propagation produces localized variations in collagen microfiber organization that in turn, promote cell behaviors essential for tissue regeneration, including cell migration and matrix remodeling. In the present study, mechanisms by which ultrasound interacts with polymerizing collagen to produce functional changes in collagen microstructure were investigated. The rate of collagen polymerization was manipulated by adjusting the pH of collagen solutions and the temperature at which gels were polymerized. Results demonstrate that the phase transition of type I collagen from fluid to gel triggered a simultaneous increase in acoustic absorption. This phase transition of collagen involves the lateral growth of early-stage collagen microfibrils and importantly, corresponded to a defined period of time during which exposure to ultrasound introduced both structural and functional changes to the resultant collagen hydrogels. Together, these experiments isolated a critical window in the collagen fiber assembly process during which mechanical forces associated with ultrasound propagation are effective in producing structural changes that underlie the ability of acoustically-modified collagen hydrogels to stimulate cell migration. These results demonstrate that changes in material properties associated with collagen polymerization are a fundamental component of the mechanism by which acoustic forces modify collagen biomaterials to enhance biological function.
最近,人们将大量注意力集中在利用细胞外基质(ECM)的成分作为各种组织工程应用和再生医学疗法的天然构建模块上。因此,人们正在寻找新的制造方法,以实现对ECM分子结构特征的分子控制,从而改善其生物学功能。将可溶性胶原蛋白暴露于与超声传播相关的声学力下,会使胶原蛋白微纤维组织产生局部变化,进而促进组织再生所必需的细胞行为,包括细胞迁移和基质重塑。在本研究中,研究了超声与聚合胶原蛋白相互作用以在胶原蛋白微观结构中产生功能变化的机制。通过调节胶原蛋白溶液的pH值和凝胶聚合的温度来控制胶原蛋白的聚合速率。结果表明,I型胶原蛋白从流体到凝胶的相变引发了声吸收的同时增加。胶原蛋白的这种相变涉及早期胶原蛋白微纤维的横向生长,重要的是,它与一个特定的时间段相对应,在此期间,暴露于超声下会给所得的胶原蛋白水凝胶带来结构和功能上的变化。总之,这些实验在胶原蛋白纤维组装过程中分离出了一个关键窗口,在此期间,与超声传播相关的机械力有效地产生了结构变化,这些结构变化是声学改性胶原蛋白水凝胶刺激细胞迁移能力的基础。这些结果表明,与胶原蛋白聚合相关的材料特性变化是声学力改变胶原蛋白生物材料以增强生物学功能的机制的一个基本组成部分。