Applying macromolecular crowding to enhance extracellular matrix deposition and its remodeling in vitro for tissue engineering and cell-based therapies

被引:146
作者
Chen, Clarice [1 ,3 ]
Loe, Felicia [1 ,3 ]
Blocki, Anna [1 ,3 ]
Peng, Yanxian [1 ]
Raghunath, Michael [1 ,2 ]
机构
[1] Natl Univ Singapore, Fac Engn, Div Bioengn, Singapore 117548, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore 117595, Singapore
[3] Natl Univ Singapore, NUS Grad Sch Engn & Integrat Sci NGS, Singapore 117548, Singapore
基金
英国医学研究理事会;
关键词
Microenvironment; Excluded volume effect; Stem cells; Differentiated cells; Matrix maturation; Collagen assembly; MESENCHYMAL STEM-CELLS; MARROW STROMAL CELLS; FIBROBLAST-GROWTH-FACTOR; BETA BINDING PROTEIN-1; V COLLAGEN FIBRILS; SELF-ASSOCIATION; DEXTRAN SULFATE; CROSS-LINKING; EX-VIVO; INTRACELLULAR ENVIRONMENT;
D O I
10.1016/j.addr.2011.03.003
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
With the advent of multicellular organisms, the exterior of the cells evolved dramatically from highly aqueous surroundings into an extracellular matrix and space crowded with macromolecules. Cell-based therapies require removal of cells from their crowded physiological context and propagating them in dilute culture medium to attain therapeutically relevant numbers whilst preserving their phenotype. However, bereft of their microenvironment, cells under perform and lose functionality. Major efforts currently aim to modify cell culture surfaces and build three dimensional scaffolds to improve this situation. We discuss here alternative strategies that enable cells to re-create their own microenvironment in vitro, using carbohydrate-based macromolecules as culture media additives that create an excluded volume effect at defined fraction volume occupancies. This biophysical approach dramatically enhances extracellular matrix deposition by differentiated cells and stem cells, and boosts progenitor cell differentiation and proliferation. We begin to understand how well cells really can perform ex vivo if given the chance. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:277 / 290
页数:14
相关论文
共 82 条
[1]
Characterization of human fibroblast-derived extracellular matrix components for human pluripotent stem cell propagation [J].
Abraham, Sheena ;
Riggs, Marion J. ;
Nelson, Kristina ;
Lee, Vladimir ;
Rao, Raj R. .
ACTA BIOMATERIALIA, 2010, 6 (12) :4622-4633
[2]
Stable Propagation of Human Embryonic and Induced Pluripotent Stem Cells on Decellularized Human Substrates [J].
Abraham, Sheena ;
Sheridan, Steven D. ;
Miller, Bradley ;
Rao, Raj R. .
BIOTECHNOLOGY PROGRESS, 2010, 26 (04) :1126-1134
[3]
Adult mesenchymal stem cells: characterization, differentiation, and application in cell and gene therapy [J].
Baksh, D ;
Song, L ;
Tuan, RS .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (03) :301-316
[4]
Proliferation kinetics and differentiation potential of ex vivo expanded human bone marrow stromal cells: Implications for their use in cell therapy [J].
Banfi, A ;
Muraglia, A ;
Dozin, B ;
Mastrogiacomo, M ;
Cancedda, R ;
Quarto, R .
EXPERIMENTAL HEMATOLOGY, 2000, 28 (06) :707-715
[5]
BATEMAN JF, 1986, J BIOL CHEM, V261, P4198
[6]
THE INFLUENCE OF MACROMOLECULAR CROWDING ON THERMODYNAMIC ACTIVITY - SOLUBILITY AND DIMERIZATION CONSTANTS FOR SPHERICAL AND DUMBBELL-SHAPED MOLECULES IN A HARD-SPHERE MIXTURE [J].
BERG, OG .
BIOPOLYMERS, 1990, 30 (11-12) :1027-1037
[7]
High-throughput screening: designer screens [J].
Blow, Nathan .
NATURE METHODS, 2009, 6 (01) :105-107
[8]
The effects of scaffold thickness on tissue engineered cartilage in photocrosslinked poly(ethylene oxide) hydrogels [J].
Bryant, SJ ;
Anseth, KS .
BIOMATERIALS, 2001, 22 (06) :619-626
[9]
Scaffolding in tissue engineering: general approaches and tissue-specific considerations [J].
Chan, B. P. ;
Leong, K. W. .
EUROPEAN SPINE JOURNAL, 2008, 17 (Suppl 4) :S467-S479
[10]
The Scar-in-a-Jar: studying potential antifibrotic compounds from the epigenetic to extracellular level in a single well [J].
Chen, C. Z. C. ;
Peng, Y. X. ;
Wang, Z. B. ;
Fish, P. V. ;
Kaar, J. L. ;
Koepsel, R. R. ;
Russell, A. J. ;
Lareu, R. R. ;
Raghunath, M. .
BRITISH JOURNAL OF PHARMACOLOGY, 2009, 158 (05) :1196-1209