Direct 3D bioprinting of perfusable vascular constructs using a blend bioink

被引:674
作者
Jia, Weitao [1 ,2 ,3 ]
Gungor-Ozkerim, P. Selcan [1 ,2 ]
Zhang, Yu Shrike [1 ,2 ,4 ]
Yue, Kan [1 ,2 ]
Zhu, Kai [1 ,2 ,5 ]
Liu, Wanjun [1 ,2 ]
Pi, Qingment [1 ,2 ]
Byambaa, Batzaya [1 ,2 ]
Dokmeci, Mehmet Remzi [1 ,2 ,4 ]
Shin, Su Ryon [1 ,2 ,4 ]
Khademhosseini, Ali [1 ,2 ,4 ,6 ,7 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Div Biomed Engn, Biomat Innovat Res Ctr,Dept Med, Cambridge, MA 02139 USA
[2] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[3] Shanghai Jiao Tong Univ, Peoples Hosp 6, Dept Orthoped Surg, Shanghai 200233, Peoples R China
[4] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
[5] Fudan Univ, Shanghai Inst Cardiovasc Dis, Zhongshan Hosp, Dept Cardiac Surg, Shanghai 200032, Peoples R China
[6] Konkuk Univ, Dept Bioind Technol, Coll Anim Biosci & Technol, Seoul 143701, South Korea
[7] King Abdulaziz Univ, Dept Phys, Jeddah 21569, Saudi Arabia
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
3D Bioprinting; Perfusable hollow tube; Bioink; Endothelial cells; Mesenchymal stem cells; MESENCHYMAL STEM-CELLS; TISSUE CONSTRUCTS; HYDROGELS; NETWORKS; EXPRESSION; STRATEGIES; SCAFFOLDS;
D O I
10.1016/j.biomaterials.2016.07.038
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Despite the significant technological advancement in tissue engineering, challenges still exist towards the development of complex and fully functional tissue constructs that mimic their natural counterparts. To address these challenges, bioprinting has emerged as an enabling technology to create highly organized three-dimensional (3D) vascular networks within engineered tissue constructs to promote the transport of oxygen, nutrients, and waste products, which can hardly be realized using conventional microfabrication techniques. Here, we report the development of a versatile 3D bioprinting strategy that employs biomimetic biomaterials and an advanced extrusion system to deposit perfusable vascular structures with highly ordered arrangements in a single-step process. In particular, a specially designed cell-responsive bioink consisting of gelatin methacryloyl (GelMA), sodium alginate, and 4-arm poly( ethylene glycol)-tetra-acrylate (PEGTA) was used in combination with a multilayered coaxial extrusion system to achieve direct 3D bioprinting. This blend bioink could be first ionically crosslinked by calcium ions followed by covalent photocrosslinking of GelMA and PEGTA to form stable constructs. The rheological properties of the bioink and the mechanical strengths of the resulting constructs were tuned by the introduction of PEGTA, which facilitated the precise deposition of complex multilayered 3D perfusable hollow tubes. This blend bioink also displayed favorable biological characteristics that supported the spreading and proliferation of encapsulated endothelial and stem cells in the bioprinted constructs, leading to the formation of biologically relevant, highly organized, perfusable vessels. These characteristics make this novel 3D bioprinting technique superior to conventional microfabrication or sacrificial templating approaches for fabrication of the perfusable vasculature. We envision that our advanced bioprinting technology and bioink formulation may also have significant potentials in engineering large-scale vascularized tissue constructs towards applications in organ transplantation and repair. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:58 / 68
页数:11
相关论文
共 66 条
  • [11] Microfl uidic Bioprinting of Heterogeneous 3D Tissue Constructs Using Low-Viscosity Bioink
    Colosi, Cristina
    Shin, Su Ryon
    Manoharan, Vijayan
    Massa, Solange
    Costantini, Marco
    Barbetta, Andrea
    Dokmeci, Mehmet Remzi
    Dentini, Mariella
    Khademhosseini, Ali
    [J]. ADVANCED MATERIALS, 2016, 28 (04) : 677 - 684
  • [12] 3D Bioprinting of heterogeneous aortic valve conduits with alginate/gelatin hydrogels
    Duan, Bin
    Hockaday, Laura A.
    Kang, Kevin H.
    Butcher, Jonathan T.
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2013, 101 (05) : 1255 - 1264
  • [13] Dvir T, 2011, NAT NANOTECHNOL, V6, P13, DOI [10.1038/nnano.2010.246, 10.1038/NNANO.2010.246]
  • [14] Elucidating the Role of Matrix Stiffness in 3D Cell Migration and Remodeling
    Ehrbar, M.
    Sala, A.
    Lienemann, P.
    Ranga, A.
    Mosiewicz, K.
    Bittermann, A.
    Rizzi, S. C.
    Weber, F. E.
    Lutolf, M. P.
    [J]. BIOPHYSICAL JOURNAL, 2011, 100 (02) : 284 - 293
  • [15] Accordion-like honeycombs for tissue engineering of cardiac anisotropy
    Engelmayr, George C., Jr.
    Cheng, Mingyu
    Bettinger, Christopher J.
    Borenstein, Jeffrey T.
    Langer, Robert
    Freed, Lisa E.
    [J]. NATURE MATERIALS, 2008, 7 (12) : 1003 - 1010
  • [16] Physiological aspects of cardiac tissue engineering
    Eschenhagen, Thomas
    Eder, Alexandra
    Vollert, Ingra
    Hansen, Arne
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2012, 303 (02): : H133 - H143
  • [17] Advanced Material Strategies for Tissue Engineering Scaffolds
    Freed, Lisa E.
    Engelmayr, George C., Jr.
    Borenstein, Jeffrey T.
    Moutos, Franklin T.
    Guilak, Forshid
    [J]. ADVANCED MATERIALS, 2009, 21 (32-33) : 3410 - 3418
  • [18] Vascular endothelial growth factor principally acts as the main angiogenic factor in the early stage of human osteoblastogenesis
    Furumatsu, T
    Shen, ZN
    Kawai, A
    Nishida, K
    Manabe, H
    Oohashi, T
    Inoue, H
    Ninomiya, Y
    [J]. JOURNAL OF BIOCHEMISTRY, 2003, 133 (05) : 633 - 639
  • [19] Coaxial nozzle-assisted 3D bioprinting with built-in microchannels for nutrients delivery
    Gao, Qing
    He, Yong
    Fu, Jian-zhong
    Liu, An
    Ma, Liang
    [J]. BIOMATERIALS, 2015, 61 : 203 - 215
  • [20] Endothelial-pericyte interactions in angiogenesis
    Gerhardt, H
    Betsholtz, C
    [J]. CELL AND TISSUE RESEARCH, 2003, 314 (01) : 15 - 23