Bioprinting of artificial blood vessels: current approaches towards a demanding goal

被引:135
作者
Hoch, Eva [1 ]
Tovar, Guenter E. M. [1 ,2 ]
Borchers, Kirsten [2 ]
机构
[1] Univ Stuttgart, Inst Interfacial Proc Engn & Plasma Technol IGVP, Nobelstr 12, D-70569 Stuttgart, Germany
[2] Fraunhofer Inst Interfacial Engn & Biotechnol IGB, D-70569 Stuttgart, Germany
关键词
Bioprinting; Tissue engineering; Artificial blood vessels; CELL ENCAPSULATION; TISSUE; SCAFFOLDS; CARTILAGE; GELATIN; FABRICATION; HYDROGELS; NETWORK; SYSTEMS; MATRIX;
D O I
10.1093/ejcts/ezu242
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Free-form fabrication techniques, often referred to as '3D printing', are currently tested with regard to the processing of biological and biocompatible materials in general and for fabrication of vessel-like structures in particular. Such computer-controlled methods assemble 3D objects by layer-wise deposition or layer-wise cross-linking of materials. They use, for example, nozzle-based deposition of hydrogels and cells, drop-on-demand inkjet-printing of cell suspensions with subsequent cross-linking, layer-by-layer cross-linking of synthetic or biological polymers by selective irradiation with light and even laser-induced deposition of single cells. The need of vessel-like structures has become increasingly crucial for the supply of encapsulated cells for 3D tissue engineering, or even with regard to future application such as vascular grafts. The anticipated potential of providing tubes with tailored branching geometries made of biocompatible or biological materials pushes future visions of patient-specific vascularized tissue substitutions, tissue-engineered blood vessels and bio-based vascular grafts. We review here the early attempts of bringing together innovative free-form manufacturing processes with bio-based and biodegradable materials. The presented studies provide many important proofs of concepts such as the possibility to integrate viable cells into computer-controlled processes and the feasibility of supplying cells in a hydrogel matrix by generation of a network of perfused channels. Several impressive results in the generation of complex shapes and high-aspect-ratio tubular structures demonstrate the potential of additive assembly methods. Yet, it also becomes obvious that there remain major challenges to simultaneously match all material requirements in terms of biological functions (cell function supporting properties), physicochemical functions (mechanical properties of the printed material) and process-related (viscosity, cross-linkability) functions, towards the demanding goal of biofabricating artificial blood vessels.
引用
收藏
页码:767 / 778
页数:12
相关论文
共 77 条
[1]   In Vivo Study of a Blended Hydrogel Composed of Pluronic F-127-Alginate-Hyaluronic Acid for its Cell Injection Application [J].
Abdi, Syed Izhar Haider ;
Choi, Jeong Yeon ;
Lee, Ji Seon ;
Lim, Hyun Ju ;
Lee, Changho ;
Kim, Jeehyun ;
Chung, Ho Yun ;
Lim, Jeong Ok .
TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2012, 9 (01) :1-9
[2]   Elastomeric degradable biomaterials by photopolymerization-based CAD-CAM for vascular tissue engineering [J].
Baudis, Stefan ;
Nehl, Franziska ;
Ligon, S. Clark ;
Nigisch, Anneliese ;
Bergmeister, Helga ;
Bernhard, David ;
Stampfl, Juergen ;
Liska, Robert .
BIOMEDICAL MATERIALS, 2011, 6 (05)
[3]   A 3D Interconnected Microchannel Network Formed in Gelatin by Sacrificial Shellac Microfibers [J].
Bellan, Leon M. ;
Pearsall, Matthew ;
Cropek, Donald M. ;
Langer, Robert .
ADVANCED MATERIALS, 2012, 24 (38) :5187-5191
[4]   Extracellular matrix scaffolds for cartilage and bone regeneration [J].
Benders, Kim E. M. ;
van Weeren, P. Rene ;
Badylak, Stephen F. ;
Saris, Daniel B. F. ;
Dhert, Wouter J. A. ;
Malda, Jos .
TRENDS IN BIOTECHNOLOGY, 2013, 31 (03) :169-176
[5]   Three-dimensional printing of stem cell-laden hydrogels submerged in a hydrophobic high-density fluid [J].
Campos, Daniela F. Duarte ;
Blaeser, Andreas ;
Weber, Michael ;
Jaekel, Joerg ;
Neuss, Sabine ;
Jahnen-Dechent, Wilhelm ;
Fischer, Horst .
BIOFABRICATION, 2013, 5 (01)
[6]   Temporal and spatial modulation of Rho GTPases during in vitro formation of capillary vascular network - Adherens junctions and myosin light chain as targets of Rac1 and RhoA [J].
Cascone, I ;
Giraudo, E ;
Caccavari, F ;
Napione, L ;
Bertotti, E ;
Collard, JG ;
Serini, G ;
Bussolino, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (50) :50702-50713
[7]   Determinants of Microvascular Network Topologies in Implanted Neovasculatures [J].
Chang, Carlos C. ;
Krishnan, Laxminarayanan ;
Nunes, Sara S. ;
Church, Kenneth H. ;
Edgar, Lowell T. ;
Boland, Eugene D. ;
Weiss, Jeffery A. ;
Williams, Stuart K. ;
Hoying, James B. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2012, 32 (01) :5-U55
[8]   Direct-write bioprinting three-dimensional biohybrid systems for future regenerative therapies [J].
Chang, Carlos C. ;
Boland, Eugene D. ;
Williams, Stuart K. ;
Hoying, James B. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2011, 98B (01) :160-170
[9]   Microfluidic scaffolds for tissue engineering [J].
Choi, Nak Won ;
Cabodi, Mario ;
Held, Brittany ;
Gleghorn, Jason P. ;
Bonassar, Lawrence J. ;
Stroock, Abraham D. .
NATURE MATERIALS, 2007, 6 (11) :908-915
[10]   Human microvasculature fabrication using thermal inkjet printing technology [J].
Cui, Xiaofeng ;
Boland, Thomas .
BIOMATERIALS, 2009, 30 (31) :6221-6227