Hench Larry L, Xynos Ionnis D, Polak Julia M
Department of Materials, Imperial College London, Prince Consort Road, London SW7 2BP, UK.
J Biomater Sci Polym Ed. 2004;15(4):543-62. doi: 10.1163/156856204323005352.
Historically the function of biomaterials has been to replace diseased or damaged tissues. Recent findings show that controlled release of the ionic dissolution products of bioactive glasses results in regeneration of tissues. The mechanism for in situ tissue regeneration involves upregulation of seven families of genes that control the osteoblast cell cycle, mitosis and differentiation. In the presence of critical concentrations of Si and Ca ions, within 48 h osteoblasts that are capable of differentiating into a mature osteocyte phenotype begin to proliferate and regenerate new bone. Osteoblasts that are not in the correct phase of the cell cycle and unable to proceed towards differentiation are switched into apoptosis by the ionic dissolution products. A controlled release of soluble Ca and Si from bioactive glass--resorbable polymer composites leads to vascularised soft tissue regeneration. Gene activation by controlled ion release provides the conceptual basis for molecular design of a third generation of biomaterials optimised for in situ tissue regeneration.
从历史角度来看,生物材料的功能一直是替代患病或受损组织。最近的研究结果表明,生物活性玻璃离子溶解产物的控释可导致组织再生。原位组织再生的机制涉及上调控制成骨细胞细胞周期、有丝分裂和分化的七个基因家族。在存在临界浓度的硅和钙离子的情况下,能够分化为成熟骨细胞表型的成骨细胞在48小时内开始增殖并再生新骨。处于细胞周期不正确阶段且无法进行分化的成骨细胞会被离子溶解产物转变为凋亡状态。生物活性玻璃-可吸收聚合物复合材料中可溶性钙和硅的控释导致血管化软组织再生。通过控释离子实现的基因激活为优化原位组织再生的第三代生物材料的分子设计提供了概念基础。