The influence of hydrogel modulus on the proliferation and differentiation of encapsulated neural stem cells

被引:521
作者
Banerjee, Akhilesh [1 ]
Arha, Manish [1 ]
Choudhary, Soumitra [2 ]
Ashton, Randolph S. [3 ,4 ]
Bhatia, Surita R. [2 ]
Schaffer, David V. [3 ,4 ]
Kane, Ravi S. [1 ]
机构
[1] Rensselaer Polytech Inst, Howard P Isermann Dept Chem & Biol Engn, Troy, NY 12180 USA
[2] Univ Massachusetts, Dept Chem Engn, Amherst, MA 01003 USA
[3] Univ Calif Berkeley, Dept Chem Engn, Dept Bioengn, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA
关键词
Alginate; Hydrogel; Modulus; Stem cells; Proliferation; Differentiation; SPINAL-CORD-INJURY; ALGINATE HYDROGELS; PHYSICAL-PROPERTIES; IN-VITRO; MATRIX; SUBSTRATE; MICROENVIRONMENTS; RESPONSES; CULTURE; BEADS;
D O I
10.1016/j.biomaterials.2009.05.050
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
There has been an increasing interest in understanding how the mechanical properties of the microenvironment influence stem cell fate. We describe studies of the proliferation and differentiation neural stem cells (NSCs) encapsulated within three-dimensional scaffolds - alginate hydrogels - whose elastic moduli were varied over two orders of magnitude. The rate of proliferation of neural stem cells decreased with increase in the modulus of the hydrogeis. Moreover, we observed the enhancement in expression of the neuronal marker beta-tubulin III within the softest hydrogels, which had an elastic modulus comparable to that of brain tissues. To our knowledge, this work represents the first demonstration of the influence of modulus on NSC differentiation in three-dimensional scaffolds. Three-dimensional scaffolds that control stem cell fate would be broadly useful for applications in regenerative medicine and tissue engineering. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4695 / 4699
页数:5
相关论文
共 41 条
[1]   Development of quantitative PCR methods to analyse neural progenitor cell culture state [J].
Abranches, E ;
O'Neill, A ;
Robertson, MJ ;
Schaffer, DV ;
Cabral, JMS .
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2006, 44 :1-8
[2]   Scaffolds based on degradable alginate hydrogels and poly(lactide-co-glycolide) microspheres for stem cell culture [J].
Ashton, Randolph S. ;
Banerjee, Akhilesh ;
Punyani, Supriya ;
Schaffer, David V. ;
Kane, Ravi S. .
BIOMATERIALS, 2007, 28 (36) :5518-5525
[3]  
Brehm Michael, 2006, Nat Clin Pract Cardiovasc Med, V3 Suppl 1, pS101
[4]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[5]   In vitro tubulogenesis of endothelial cells by relaxation of the coupling extracellular matrix-cytoskeleton [J].
Deroanne, CF ;
Lapiere, CM ;
Nusgens, BV .
CARDIOVASCULAR RESEARCH, 2001, 49 (03) :647-658
[6]   PERIVASCULAR AND INTRAVENOUS ADMINISTRATION OF BASIC FIBROBLAST GROWTH-FACTOR - VASCULAR AND SOLID ORGAN DEPOSITION [J].
EDELMAN, ER ;
NUGENT, MA ;
KARNOVSKY, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (04) :1513-1517
[7]   Substrate compliance versus ligand density in cell on gel responses [J].
Engler, A ;
Bacakova, L ;
Newman, C ;
Hategan, A ;
Griffin, M ;
Discher, D .
BIOPHYSICAL JOURNAL, 2004, 86 (01) :617-628
[8]   Matrix elasticity directs stem cell lineage specification [J].
Engler, Adam J. ;
Sen, Shamik ;
Sweeney, H. Lee ;
Discher, Dennis E. .
CELL, 2006, 126 (04) :677-689
[9]   Myotubes differentiate optimally on substrates with tissue-like stiffness:: pathological implications for soft or stiff microenvironments [J].
Engler, AJ ;
Griffin, MA ;
Sen, S ;
Bönnetnann, CG ;
Sweeney, HL ;
Discher, DE .
JOURNAL OF CELL BIOLOGY, 2004, 166 (06) :877-887
[10]   Neurite branching on deformable substrates [J].
Flanagan, LA ;
Ju, YE ;
Marg, B ;
Osterfield, M ;
Janmey, PA .
NEUROREPORT, 2002, 13 (18) :2411-2415