Bioprinting three-dimensional cell-laden tissue constructs with controllable degradation

Scientific Reports

Volumn 6, Issue , 2016, Pages

  Wu, Zhengjie ^a   Su, Xin ^a   Xu, Yuanyuan ^a   Kong, Bin ^a   Sun, Wei ^a,b   Mi, Shengli ^a  

^a TSINGHUA UNIVERSITY   (China)

^b Drexel University   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALGINIC ACID; COLLAGEN; GELATIN; GLUCURONIC ACID; HEXURONIC ACID; HYDROGEL;

BIOPRINTING; CELL PROLIFERATION; CELL SURVIVAL; CHEMISTRY; CORNEA EPITHELIUM; CYTOLOGY; DRUG EFFECTS; HUMAN; HYDROGEL; PROCEDURES; THREE DIMENSIONAL PRINTING; TISSUE ENGINEERING; TISSUE SCAFFOLD;

ALGINATES; BIOPRINTING; CELL PROLIFERATION; CELL SURVIVAL; COLLAGEN; EPITHELIUM, CORNEAL; GELATIN; GLUCURONIC ACID; HEXURONIC ACIDS; HUMANS; HYDROGEL; PRINTING, THREE-DIMENSIONAL; TISSUE ENGINEERING; TISSUE SCAFFOLDS;

EID: 84973370305     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep24474     Document Type: Article

References (48)

1. Derby, B. Printing and prototyping of tissues and scaffolds. Science. 338, 921-926 (2012).
2. Atala, A. Tissue engineering and regenerative medicine: concepts for clinical application. Rejuv. Res. 7, 15-31 (2004).
3. Hollister, S. J. Porous scaffold design for tissue engineering. Nat. mater. 4, 518-524 (2005).
4. Hutmacher, D. W. Scaffolds in tissue engineering bone and cartilage. Biomaterials. 21, 2529-2543 (2000).
5. Reiffel, A. J. et al. High-fidelity tissue engineering of patient-specific auricles for reconstruction of pediatric microtia and other auricular deformities. PloS one. 8, e56506 (2013).
6. Cohen, D. L. et al. Direct freeform fabrication of seeded hydrogels in arbitrary geometries. Tissue Eng. 12, 1325-1335 (2006).
7. Mironov, V. et al. Organ printing: tissue spheroids as building blocks. Biomaterials. 30, 2164-2174 (2009).
8. Mannoor, M. S. et al. 3D printed bionic ears. Nano Lett. 13, 2634-2639 (2013).
9. Norotte, C. et al. Scaffold-free vascular tissue engineering using bioprinting. Biomaterials. 30, 5910-5917 (2009).
10. Ferris, C. J., Gilmore, K. G. & Wallace, G. G. Biofabrication: an overview of the approaches used for printing of living cells. Appl. Microbiol. Biotechnol. 97, 4243-4258 (2013).
11. Pati, F. et al. Printing three-dimensional tissue analogues with decellularized extracellular matrix bioink. Nat. Commun. 5, 3935-3945 (2014).
12. Wang, X. et al. Generation of three-dimensional hepatocyte/gelatin structures with rapid prototyping system. Tissue Egn. 12, 83-90 (2006).
13. Chang, R., Nam, J. & Sun, W. Effects of dispensing pressure and nozzle diameter on cell survival from solid freeform fabricationbased direct cell writing. Tissue Eng Part A. 14, 41-48 (2008).
14. Yan, Y. et al. Direct construction of a three-dimensional structure with cells and hydrogel. J. Bioact. Compat. Polym. 20, 259-269 (2005).
15. Xu, W. et al. Rapid prototyping three-dimensional cell/gelatin/fibrinogen constructs for medical regeneration. J. Bioact. Compat. Polym. 22, 363-377 (2007).
16. Rutz, A. L. et al. A Multimaterial Bioink Method for 3D Printing Tunable, Cell-Compatible Hydrogels. Adv. Mater. 27, 1607-1614 (2015).
17. Cohen, D. L. et al. Improved quality of 3D-printed tissue constructs through enhanced mixing of alginate hydrogels. C. Proceedings of the 19th Solid Freeform Fabrication Symposium. 4-6(2008).
18. Smrdel, P. et al. Characterization of calcium alginate beads containing structurally similar drugs. Drug Dev. Ind. Pharm. 32. 623-633 (2006).
19. Rowley, J. A., Madlambayan, G. & Mooney, D. J. Alginate hydrogels as synthetic extracellular matrix materials. Biomaterials. 20, 45-53 (1999).
20. Lee, K. Y. & Mooney, D. J. Alginate: properties and biomedical applications. Prog. Polym. Sci. 37, 106-126 (2012).
21. Derby, B. Bioprinting: inkjet printing proteins and hybrid cell-containing materials and structures. J. Mater. Chem. 18, 5717-5721 (2008).
22. Grigore, A. et al. Behavior of encapsulated MG-63 cells in RGD and gelatine-modified alginate hydrogels. Tissue Eng Part A. 20, 2140-2150 (2014).
23. Schloßmacher, U. et al. Alginate/silica composite hydrogel as a potential morphogenetically active scaffold for three-dimensional tissue engineering. RSC Adv. 3, 11185-11194 (2013).
24. Shoichet, M. S. et al. Stability of hydrogels used in cell encapsulation: An in vitro comparison of alginate and agarose. Biotechnol. Bioeng. 50, 374-381 (1996).
25. Visser. J. et al. Biofabrication of multi-material anatomically shaped tissue constructs. Biofabrication. 5, 035007 (2013).
26. Kim, G. H. et al. Coaxial structured collagen-alginate scaffolds: fabrication, physical properties, and biomedical application for skin tissue regeneration. J. Mater. Chem. 21, 6165-6172 (2011).
27. Xu, T. et al. Complex heterogeneous tissue constructs containing multiple cell types prepared by inkjet printing technology. Biomaterials, 34, 130-139 (2013).
28. Ortega, I. et al. Combined microfabrication and electrospinning to produce 3-D architectures for corneal repair. Acta Biomater. 9, 5511-5520 (2013).
29. Ghezzi, C. E., Rnjak, K. J. & Kaplan, D. L. Corneal tissue engineering: recent advances and future perspectives. Tissue Eng Part B. 21, 278-287 (2015).
30. Feng, Y. et al. Influence of substrate on corneal epithelial cell viability within ocular surface models. Exp. Eye. Res. 101, 97-103 (2012).
31. Dua, H. S. et al. Limbal epithelial crypts: a novel anatomical structure and a putative limbal stem cell niche. Br. J. Ophthalmol. 89, 529-532 (2005).
32. Mi, S. L. et al. Reconstruction of corneal epithelium with cryopreserved corneal limbal stem cells in a goat model. Mol. Reprod. Dev. 75, 1607-1616 (2008).
33. Qu, L. et al. Reconstruction of corneal epithelium with cryopreserved corneal limbal stem cells in a rabbit model. VET.J. 179, 392-400 (2009).
34. Connon, C. J. et al. Gene expression and immunolocalisation of a calcium-activated chloride channel during the stratification of cultivated and developing corneal epithelium. Cell Tissue Res. 323, 177-182 (2006).
35. Yang, X. et al. Reconstruction of damaged cornea by autologous transplantation of epidermal adult stem cells. Mol. Vis, 14, 1064 (2008).
36. Ouyang, L. L. et al. 3D printing of HEK 293FT cell-laden hydrogel into macroporous constructs with high cell viability and normal biological functions. Biofabrication. 7, 015010 (2015).
37. Zhao, Y. et al. Three-dimensional printing of Hela cells for cervical tumor model in vitro. Biofabrication. 6, 035001 (2014).
38. Araki-Sasaki, K. et al. An SV40-immortalized human corneal epithelial cell line and its characterization. Invest. Ophthalmol. Vis. Sci. 36, 614 (1995).
39. Wright, B., Mi, S. L. & Connon C.J., Towards the use of hydrogels in the treatment of limbal stem cell deficiency. Drug Discov. Today. 18, 79-86 (2013).
40. Xu, M. E. et al. An cell-assembly derived physiological 3D model of the metabolic syndrome, based on adipose-derived stromal cells and a gelatin/alginate/fibrinogen matrix. Biomaterials. 31, 3868-3877 (2010).
41. Duan, B. et al. 3D bioprinting of heterogeneous aortic valve conduits with alginate/gelatin hydrogels. J. Biomed. Mater Res Part A. 101, 1255-1264 (2013).
42. Pati, F. et al. Biomimetic 3D Tissue Printing for Soft Tissue Regeneration. Biomaterials. 62, 164-175 (2015).
43. Das, S. et al. Bioprintable, cell-laden silk fibroin-gelatin hydrogel supporting multilineage differentiation of stem cells for fabrication of three-dimensional tissue constructs. Acta Biomater. 11, 233-246 (2015).
44. Fedorovich, N. E. et al. Three-dimensional fiber deposition of cell-laden, viable, patterned constructs for bone tissue printing. Tissue Eng Part A. 14, 127-33(2008).
45. Loessner, D. et al. Bioengineered 3D platform to explore cell-ECM interactions and drug resistance of epithelial ovarian cancer cells. Biomaterials. 31, 8494-8506 (2010).
46. Amsellem, S. et al. Ex vivo expansion of human hematopoietic stem cells by direct delivery of the HOXB4 homeoprotein. Nat. Med. 9, 1423-1427 (2003).
47. Chayosumrit, M., Tuch, B. & Sidhu, K. Alginate microcapsule for propagation and directed differentiation of hESCs to definitive endoderm. Biomaterials. 31, 505-514 (2010).
48. Hunt, N. C. et al. Encapsulation of fibroblasts causes accelerated alginate hydrogel degradation. Acta Biomater. 6, 3649-3656 (2010).