Efficient generation of hPSC-derived midbrain dopaminergic neurons in a fully defined, scalable, 3D biomaterial platform

被引:46
作者
Adil, Maroof M. [1 ]
Rodrigues, Gonalo M. C. [1 ]
Kulkarni, Rishikesh U. [2 ]
Rao, Antara T. [1 ]
Chernavsky, Nicole E. [1 ]
Miller, Evan W. [2 ,3 ,4 ]
Schaffer, David V. [1 ,3 ,4 ,5 ]
机构
[1] Univ Calif Berkeley, Dept Biomol & Chem Engn, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Mol & Cell Biol, 229 Stanley Hall, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA
[5] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
关键词
EMBRYONIC STEM-CELLS; HUMAN ES; SUSPENSION-CULTURE; RAT MODEL; DIFFERENTIATION; EXPANSION; PROGENITORS; VOLTAGE; GRAFTS; SYSTEM;
D O I
10.1038/srep40573
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Pluripotent stem cells (PSCs) have major potential as an unlimited source of functional cells for many biomedical applications; however, the development of cell manufacturing systems to enable this promise faces many challenges. For example, there have been major recent advances in the generation of midbrain dopaminergic (mDA) neurons from stem cells for Parkinson's Disease (PD) therapy; however, production of these cells typically involves undefined components and difficult to scale 2D culture formats. Here, we used a fully defined, 3D, thermoresponsive biomaterial platform to rapidly generate large numbers of action-potential firing mDA neurons after 25 days of differentiation (similar to 40% tyrosine hydroxylase (TH) positive, maturing into 25% cells exhibiting mDA neuron-like spiking behavior). Importantly, mDA neurons generated in 3D exhibited a 30-fold increase in viability upon implantation into rat striatum compared to neurons generated on 2D, consistent with the elevated expression of survival markers FOXA2 and EN1 in 3D. A defined, scalable, and resource-efficient cell culture platform can thus rapidly generate high quality differentiated cells, both neurons and potentially other cell types, with strong potential to accelerate both basic and translational research.
引用
收藏
页数:11
相关论文
共 53 条
[1]
Midbrain dopamine neuron differentiation: Factors and fates [J].
Abeliovich, Asa ;
Hammond, Rachel .
DEVELOPMENTAL BIOLOGY, 2007, 304 (02) :447-454
[2]
Dynamic suspension culture for scalable expansion of undifferentiated human pluripotent stem cells [J].
Amit, Michal ;
Laevsky, Ilana ;
Miropolsky, Yael ;
Shariki, Kohava ;
Peri, Meital ;
Itskovitz-Eldor, Joseph .
NATURE PROTOCOLS, 2011, 6 (05) :572-579
[3]
Transcriptional control of midbrain dopaminergic neuron development [J].
Ang, Siew-Lan .
DEVELOPMENT, 2006, 133 (18) :3499-3506
[4]
[Anonymous], 2014, Stem Cells
[5]
[Anonymous], 1995, Psychopharmacology
[6]
How to make a midbrain dopaminergic neuron [J].
Arenas, Ernest ;
Denham, Mark ;
Villaescusa, J. Carlos .
DEVELOPMENT, 2015, 142 (11) :1918-1936
[7]
Small functional groups for controlled differentiation of hydrogel-encapsulated human mesenchymal stem cells [J].
Benoit, Danielle S. W. ;
Schwartz, Michael P. ;
Durney, Andrew R. ;
Anseth, Kristi S. .
NATURE MATERIALS, 2008, 7 (10) :816-823
[8]
Transcriptome analysis reveals transmembrane targets on transplantable midbrain dopamine progenitors [J].
Bye, Chris R. ;
Jonsson, Marie E. ;
Bjorklund, Anders ;
Parish, Clare L. ;
Thompson, Lachlan H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (15) :E1946-E1955
[9]
Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling [J].
Chambers, Stuart M. ;
Fasano, Christopher A. ;
Papapetrou, Eirini P. ;
Tomishima, Mark ;
Sadelain, Michel ;
Studer, Lorenz .
NATURE BIOTECHNOLOGY, 2009, 27 (03) :275-280
[10]
Temporal application of topography to increase the rate of neural differentiation from human pluripotent stem cells [J].
Chan, Lesley Y. ;
Birch, William R. ;
Yim, Evelyn K. F. ;
Choo, Andre B. H. .
BIOMATERIALS, 2013, 34 (02) :382-392