siRNA Nanoparticle Functionalization of Nanostructured Scaffolds Enables Controlled Multilineage Differentiation of Stem Cells

被引:67
作者
Andersen, Morten O. [1 ,2 ]
Nygaard, Jens V. [1 ]
Burns, Jorge S. [6 ]
Raarup, Merete K. [3 ,4 ]
Nyengaard, Jens R. [3 ,4 ]
Bunger, Cody [5 ]
Besenbacher, Flemming [1 ]
Howard, Kenneth A. [1 ,2 ]
Kassem, Moustapha [6 ,7 ]
Kjems, Jorgen [1 ,2 ]
机构
[1] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, Dept Mol Biol, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ, Stereol & Electron Microscopy Lab, DK-8000 Aarhus C, Denmark
[4] Aarhus Univ, MIND Ctr, DK-8000 Aarhus C, Denmark
[5] Aarhus Univ, Orthopaed Res Lab, DK-8000 Aarhus C, Denmark
[6] Odense Univ Hosp, Dept Endocrinol & Metab, DK-5000 Odense C, Denmark
[7] King Saud Univ, Coll Med, Stem Cell Unit, Dept Anat, Riyadh 11461, Saudi Arabia
基金
英国医学研究理事会;
关键词
SUPPRESSES ADIPOCYTE DIFFERENTIATION; IN-VIVO; TRANSCRIPTIONAL ACTIVITY; C/EBP-BETA; DELIVERY; GENE; EXPRESSION; MECHANISM; REGENERATION; FIBROBLASTS;
D O I
10.1038/mt.2010.166
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The creation of complex tissues and organs is the ultimate goal in tissue engineering. Engineered morphogenesis necessitates spatially controlled development of multiple cell types within a scaffold implant. We present a novel method to achieve this by adhering nanoparticles containing different small-interfering RNAs (siRNAs) into nanostructured scaffolds. This allows spatial retention of the RNAs within nanopores until their cellular delivery. The released siRNAs were capable of gene silencing BCL2L2 and TRIB2, in mesenchymal stem cells (MSCs), enhancing osteogenic and adipogenic differentiation, respectively. This approach for enhancing a single type of differentiation is immediately applicable to all areas of tissue engineering. Different nanoparticles localized to spatially distinct locations within a single implant allowed two different tissue types to develop in controllable areas of an implant. As a consequence of this, we predict that complex tissues and organs can be engineered by the in situ development of multiple cell types guided by spatially restricted nanoparticles.
引用
收藏
页码:2018 / 2027
页数:10
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