Emulating human microcapillaries in a multi-organ-chip platform

被引:34
|
作者
Hasenberg, Tobias [1 ,2 ]
Muehleder, Severin [3 ,4 ]
Dotzler, Andrea [1 ,2 ]
Bauer, Sophie [1 ]
Labuda, Krystyna [3 ,4 ]
Holnthoner, Wolfgang [3 ,4 ]
Redl, Heinz [3 ,4 ]
Lauster, Roland [1 ]
Marx, Uwe [1 ,2 ]
机构
[1] Tech Univ Berlin, Med Biotechnol, D-13355 Berlin, Germany
[2] TissUse GmbH, D-15528 Spreenhagen, Germany
[3] Ludwig Boltzmann Inst Expt & Clin Traumatol, A-1200 Vienna, Austria
[4] Austrian Cluster Tissue Regenerat, Vienna, Austria
关键词
Multi-organ-chip; Vasculature; Vasculogenesis; Fibrin scaffold; Tissue engineering; Co-culture models; MESENCHYMAL STEM-CELLS; LAMINAR SHEAR-STRESS; ENDOTHELIAL-CELLS; IN-VITRO; GENE-EXPRESSION; MICROVASCULAR NETWORKS; EXTRACELLULAR-MATRIX; CAPILLARY NETWORKS; TISSUE; VASCULOGENESIS;
D O I
10.1016/j.jbiotec.2015.09.038
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
Current microfluidic chip-based tissue culture systems lack a capillary endothelial vessel system, which would enable perfusion with blood. We utilise spatial cell cultures to populate a perfused multi-organ-chip platform a microfluidic device recently introduced for substance testing. Complete biological vascularization of such culture systems is vital to properly emulate physiological tissue behaviour. In this study, we incorporated a fibrin scaffold into the two-organ-chip design. Herein, adipose-derived stromal cells (ASCs) directed human umbilical vein endothelial cells (HUVECs) to organise into tube-like structures. The ASCs induced tube formation of HUVECs in static and dynamic conditions. The replacement of full medium enriched with growth factors and foetal calf serum with basal medium resulted in viable cells with similar gene expression profiles. We regard this as a prerequisite for studies with organ constructs that have a need for a different medium formulation. Furthermore, we here address stability issues of the fibrin gel and fibrin composition for optimal microvessel formation. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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