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A Genetic Basis for Design of Biomaterials For In Situ Tissue Regeneration

机译:用于原位组织再生的生物材料设计的遗传基础

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Historically the function of biomaterials has been to replace diseased, damaged and aged tissues. First generation biomaterials, including bio ceramics, were selected to be as inert as possible in order to minimize the thickness of interfacial scar tissue. Bioactive glasses provided an alternative from the 1970's onward; second generation bioactive bonding of implants with tissues and no interfacial scar tissue. This chapter reviews the discovery that controlled release of biologically active Ca and Si ions from bioactive glasses leads to the up-regulation and activation of seven families of genes in osteoprogenitor cells that give rise to rapid bone regeneration. This finding offers the possibility of creating a new generation of gene activating bioceramics designed specially for tissue engineering and in situ regeneration of tissues.
机译:历史上,生物材料的功能一直是取代患病,受损和老年的组织。将第一代生物材料(包括BIO陶瓷)选择为尽可能地惰性,以最小化界面瘢痕组织的厚度。生物活跃的眼镜提供了1970年代的替代方案;第二代生物活性粘合植入物与组织和没有界面瘢痕组织。本章综述,从生物活性玻璃中控制释放生物活性CA和Si离子的发现导致骨培养剂细胞中七个基因的上调和激活,从而产生快速骨再生。该发现提供了创建新一代基因激活生物陶瓷,专门用于组织工程和原位再生组织。

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