Organ engineering based on decellularized matrix scaffolds

被引:437
作者
Song, Jeremy J. [1 ]
Ott, Harald C. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Surg, Boston, MA 02114 USA
关键词
EXTRACELLULAR-MATRIX; CARDIAC TISSUE; IN-VITRO; GROWTH-FACTORS; CELLS; KIDNEY; REPAIR; HEART; LUNG; INDUCTION;
D O I
10.1016/j.molmed.2011.03.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
End-organ failure is one of the major healthcare challenges in the Western world. Yet, donor organ shortage and the need for immunosuppression limit the impact of transplantation. The regeneration of whole organs could theoretically overcome these hurdles. Early milestones have been met by combining stem and progenitor cells with increasingly complex scaffold materials and culture conditions. Because the native extracellular matrix (ECM) guides organ development, repair and physiologic regeneration, it provides a promising alternative to synthetic scaffolds and a foundation for regenerative efforts. Perfusion decellularization is a novel technology that generates native ECM scaffolds with intact 3D anatomical architecture and vasculature. This review summarizes achievements to date and discusses the role of native ECM scaffolds in organ regeneration.
引用
收藏
页码:424 / 432
页数:9
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