Ehrbar Martin, Rizzi Simone C, Hlushchuk Ruslan, Djonov Valentin, Zisch Andreas H, Hubbell Jeffrey A, Weber Franz E, Lutolf Matthias P
Oral Biology, Section Bioengineering, Department of Cranio-Maxillofacial Surgery, University Hospital Zurich, Zurich, Switzerland.
Biomaterials. 2007 Sep;28(26):3856-66. doi: 10.1016/j.biomaterials.2007.03.027. Epub 2007 Apr 5.
The molecular engineering of cell-instructive artificial extracellular matrices is a powerful means to control cell behavior and enable complex processes of tissue formation and regeneration. This work reports on a novel method to produce such smart biomaterials by recapitulating the crosslinking chemistry and the biomolecular characteristics of the biopolymer fibrin in a synthetic analog. We use activated coagulation transglutaminase factor XIIIa for site-specific coupling of cell adhesion ligands and engineered growth factor proteins to multiarm poly(ethylene glycol) macromers that simultaneously form proteolytically sensitive hydrogel networks in the same enzyme-catalyzed reaction. Growth factor proteins are quantitatively incorporated and released upon cell-derived proteolytic degradation of the gels. Primary stromal cells can invade and proteolytically remodel these networks both in an in vitro and in vivo setting. The synthetic ease and potential to engineer their physicochemical and bioactive characteristics makes these hybrid networks true alternatives for fibrin as provisional drug delivery platforms in tissue engineering.
具有细胞指导作用的人工细胞外基质的分子工程是控制细胞行为以及实现组织形成和再生复杂过程的有力手段。这项工作报道了一种通过在合成类似物中重现生物聚合物纤维蛋白的交联化学和生物分子特征来生产此类智能生物材料的新方法。我们使用活化的凝血转谷氨酰胺酶因子XIIIa将细胞粘附配体和工程化生长因子蛋白位点特异性偶联到多臂聚乙二醇大分子单体上,这些大分子单体在同一酶催化反应中同时形成对蛋白水解敏感的水凝胶网络。生长因子蛋白在凝胶被细胞衍生的蛋白水解降解时被定量掺入并释放。原代基质细胞在体外和体内环境中都能侵入并通过蛋白水解作用重塑这些网络。合成的简易性以及对其物理化学和生物活性特征进行工程改造的潜力,使得这些混合网络成为纤维蛋白在组织工程中作为临时药物递送平台的真正替代品。