A matrigel-free method to generate matured human cerebral organoids using 3D-Printed microwell arrays

被引:62
作者
Chen, Cheng [1 ]
Rengarajan, Venkatakrishnan [1 ]
Kjar, Andrew [1 ]
Huang, Yu [1 ]
机构
[1] Utah State Univ, Dept Biol Engn, Logan, UT 84322 USA
关键词
Cortical wrinkling; Cortical folding; 3D culture; Biomanufacturing; Embryoid body spheroid; Microfabrication; HUMAN BRAIN ORGANOIDS; SELF-ORGANIZATION; MODEL; PDMS; SIZE; NEUROGENESIS; STABILITY; EVOLUTION; CULTURE; SYSTEM;
D O I
10.1016/j.bioactmat.2020.10.003
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The current methods of generating human cerebral organoids rely excessively on the use of Matrigel or other external extracellular matrices (ECM) for cell micro-environmental modulation. Matrigel embedding is problematic for long-term culture and clinical applications due to high inconsistency and other limitations. In this study, we developed a novel micmwell culture platform based on 3D printing. This platform, without using Matrigel or external signaling molecules (i.e., SMAD and Wnt inhibitors), successfully generated matured human cerebral organoids with robust formation of high-level features (i.e., wrinkling/folding, lumens, neuronal layers). The formation and timing were comparable or superior to the current Matrigel methods, yet with improved consistency. The effect of microwell geometries (curvature and resolution) and coating materials (i.e., mPEG, Lipidure, BSA) was studied, showing that mPEG outperformed all other coating materials, while curved-bottom microwells outperformed flat-bottom ones. In addition, high-resolution printing outperformed low-resolution printing by creating faithful, isotropically-shaped microwells. The trend of these effects was consistent across all developmental characteristics, including EB formation efficiency and sphericity, organoid size, wrinkling index, lumen size and thickness, and neuronal layer thickness. Overall, the micmwell device that was mPEG-coated, high-resolution printed, and bottom curved demonstrated the highest efficacy in promoting organoid development. This platform provided a promising strategy for generating uniform and mature human cerebral organoids as an alternative to Matrigel/ECM-embedding methods.
引用
收藏
页码:1130 / 1139
页数:10
相关论文
共 82 条
[11]   The use of brain organoids to investigate neural development and disease [J].
Di Lullo, Elizabeth ;
Kriegstein, Arnold R. .
NATURE REVIEWS NEUROSCIENCE, 2017, 18 (10) :573-584
[12]   Surface modification with BSA blocking based on in situ synthesized gold nanoparticles in poly(dimethylsiloxane) microchip [J].
Fan, Da-He ;
Yuan, Shi-Wei ;
Shen, Yong-Miao .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2010, 75 (02) :608-611
[13]   Three-Dimensional Cell Cultures in Drug Discovery and Development [J].
Fang, Ye ;
Eglen, Richard M. .
SLAS DISCOVERY, 2017, 22 (05) :456-472
[14]   Neural progenitors, neurogenesis and the evolution of the neocortex [J].
Florio, Marta ;
Huttner, Wieland B. .
DEVELOPMENT, 2014, 141 (11) :2182-2194
[15]   Simple Surface Modification of Poly(dimethylsiloxane) via Surface Segregating Smart Polymers for Biomicrofluidics [J].
Gokaltun, Aslihan ;
Kang, Young Bok ;
Yarmush, Martin L. ;
Usta, O. Berk ;
Asatekin, Ayse .
SCIENTIFIC REPORTS, 2019, 9 (1)
[16]   Nonlinear 3D projection printing of concave hydrogel microstructures for long-term multicellular spheroid and embryoid body culture [J].
Hribar, K. C. ;
Finlay, D. ;
Ma, X. ;
Qu, X. ;
Ondeck, M. G. ;
Chung, P. H. ;
Zanella, F. ;
Engler, A. J. ;
Sheikh, F. ;
Vuori, K. ;
Chen, S. C. .
LAB ON A CHIP, 2015, 15 (11) :2412-2418
[17]  
Hribar K.C., 2019, METHOD FABRICATION M
[18]   Spherical microwell arrays for studying single cells and microtissues in 3D confinement [J].
Huang, Cheng-Kuang ;
Paylaga, Giovanni J. ;
Bupphathong, Sasinan ;
Lin, Keng-Hui .
BIOFABRICATION, 2020, 12 (02)
[19]   Microwell-mediated control of embryoid body size regulates embryonic stem cell fate via differential expression of WNT5a and WNT11 [J].
Hwang, Yu-Shik ;
Chung, Bong Geun ;
Ortmann, Daniel ;
Hattori, Nobuaki ;
Moeller, Hannes-Christian ;
Khademhosseini, Ali .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (40) :16978-16983
[20]   Type I Collagen as an Extracellular Matrix for the In Vitro Growth of Human Small Intestinal Epithelium [J].
Jabaji, Ziyad ;
Brinkley, Garrett J. ;
Khalil, Hassan A. ;
Sears, Connie M. ;
Lei, Nan Ye ;
Lewis, Michael ;
Stelzner, Matthias ;
Martin, Martin G. ;
Dunn, James C. Y. .
PLOS ONE, 2014, 9 (09)