Lutolf Matthias P, Weber Franz E, Schmoekel Hugo G, Schense Jason C, Kohler Thomas, Müller Ralph, Hubbell Jeffrey A
Institute for Biomedical Engineering, Swiss Federal Institute of Technology, Zurich and University of Zurich, Zurich, Switzerland.
Nat Biotechnol. 2003 May;21(5):513-8. doi: 10.1038/nbt818. Epub 2003 Apr 21.
We have engineered synthetic poly(ethylene glycol) (PEG)-based hydrogels as cell-ingrowth matrices for in situ bone regeneration. These networks contain a combination of pendant oligopeptide ligands for cell adhesion (RGDSP) and substrates for matrix metalloproteinase (MMP) as linkers between PEG chains. Primary human fibroblasts were shown to migrate within these matrices by integrin- and MMP-dependent mechanisms. Gels used to deliver recombinant human bone morphogenetic protein-2 (rhBMP-2) to the site of critical- sized defects in rat crania were completely infiltrated by cells and were remodeled into bony tissue within five weeks. Bone regeneration was dependent on the proteolytic sensitivity of the matrices and their architecture. The cell-mediated proteolytic invasiveness of the gels and entrapment of rhBMP-2 resulted in efficient and highly localized bone regeneration.
我们设计了基于合成聚乙二醇(PEG)的水凝胶作为用于原位骨再生的细胞生长基质。这些网络包含用于细胞黏附的侧链寡肽配体(RGDSP)和作为PEG链之间连接体的基质金属蛋白酶(MMP)底物的组合。原代人成纤维细胞通过整合素和MMP依赖性机制在这些基质内迁移。用于将重组人骨形态发生蛋白-2(rhBMP-2)递送至大鼠颅骨临界尺寸缺损部位的凝胶被细胞完全浸润,并在五周内重塑为骨组织。骨再生取决于基质的蛋白水解敏感性及其结构。凝胶的细胞介导的蛋白水解侵袭性和rhBMP-2的包封导致了高效且高度局部化的骨再生。