Bioreactors to influence stem cell fate: Augmentation of mesenchymal stem cell signaling pathways via dynamic culture systems

被引:96
作者
Yeatts, Andrew B. [1 ]
Choquette, Daniel T. [1 ]
Fisher, John P. [1 ]
机构
[1] Univ Maryland, Fischell Dept Bioengn, College Pk, MD 20742 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2013年 / 1830卷 / 02期
基金
美国国家卫生研究院;
关键词
Bioreactor; Mesenchymal stem cell; Cell signaling; Shear; Oxygen tension; ACTIVATED PROTEIN-KINASE; MARROW STROMAL CELLS; GROWTH-FACTOR-BETA; HYPOXIA-INDUCIBLE FACTOR; TISSUE-ENGINEERED BONE; MINERALIZED MATRIX DEPOSITION; REDUCED OXYGEN-TENSION; FLOW PERFUSION CULTURE; INDUCED SHEAR-STRESS; OSTEOGENIC DIFFERENTIATION;
D O I
10.1016/j.bbagen.2012.06.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Background: Mesenchymal stem cells (MSCs) are a promising cell source for bone and cartilage tissue engineering as they can be easily isolated from the body and differentiated into osteoblasts and chondrocytes. A cell based tissue engineering strategy using MSCs often involves the culture of these cells on three-dimensional scaffolds; however the size of these scaffolds and the cell population they can support can be restricted in traditional static culture. Thus dynamic culture in bioreactor systems provides a promising means to culture and differentiate MSCs in vitro. Scope of review: This review seeks to characterize key MSC differentiation signaling pathways and provides evidence as to how dynamic culture is augmenting these pathways. Following an overview of dynamic culture systems, discussion will be provided on how these systems can effectively modify and maintain important culture parameters including oxygen content and shear stress. Literature is reviewed for both a highlight of key signaling pathways and evidence for regulation of these signaling pathways via dynamic culture systems. Major conclusions: The ability to understand how these culture systems are affecting MSC signaling pathways could lead to a shear or oxygen regime to direct stem cell differentiation. In this way the efficacy of in vitro culture and differentiation of MSCs on three-dimensional scaffolds could be greatly increased. General significance: Bioreactor systems have the ability to control many key differentiation stimuli including mechanical stress and oxygen content. The further integration of cell signaling investigations within dynamic culture systems will lead to a quicker realization of the promise of tissue engineering and regenerative medicine. This article is part of a Special Issue entitled Biochemistry of Stem Cells. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:2470 / 2480
页数:11
相关论文
共 150 条
[1]
Evidence for a role of MSK1 in transforming growth factor-β-mediated responses through p38α and Smad signaling pathways [J].
Abécassis, L ;
Rogier, E ;
Vazquez, A ;
Atfi, A ;
Bourgeade, MF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (29) :30474-30479
[2]
Shear-induced cyclooxygenase-2 via a JNK2/c-Jun-dependent pathway regulates prostaglandin receptor expression in chondrocytic cells [J].
Abulencia, JP ;
Gaspard, R ;
Healy, ZR ;
Gaarde, WA ;
Quackenbush, J ;
Konstantopoulos, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (31) :28388-28394
[3]
Smad function and intranuclear targeting share a Runx2 motif required for osteogenic lineage induction and BMP2 responsive transcription [J].
Afzal, F ;
Pratap, J ;
Ito, K ;
Ito, Y ;
Stein, JL ;
Van Winen, AJ ;
Stein, GS ;
Lian, JB ;
Javed, A .
JOURNAL OF CELLULAR PHYSIOLOGY, 2005, 204 (01) :63-72
[4]
Interactions between Sox9 and β-catenin control chondrocyte differentiation [J].
Akiyama, H ;
Lyons, JP ;
Mori-Akiyama, Y ;
Yang, XH ;
Zhang, R ;
Zhang, ZP ;
Deng, JM ;
Taketo, MM ;
Nakamura, T ;
Behringer, RR ;
McCrea, PD ;
de Crombrugghe, B .
GENES & DEVELOPMENT, 2004, 18 (09) :1072-1087
[5]
Chondrogenic differentiation of human bone marrow mesenchymal stem cells in chitosan-based scaffolds using a flow-perfusion bioreactor [J].
Alves da Silva, M. L. ;
Martins, A. ;
Costa-Pinto, A. R. ;
Correlo, V. M. ;
Sol, P. ;
Bhattacharya, M. ;
Faria, S. ;
Reis, R. L. ;
Neves, N. M. .
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2011, 5 (09) :722-732
[6]
Regulation of bone morphogenetic protein-2 expression by endogenous prostaglandin E2 in human mesenchymal stem cells [J].
Arikawa, T ;
Omura, K ;
Morita, I .
JOURNAL OF CELLULAR PHYSIOLOGY, 2004, 200 (03) :400-406
[7]
Non-Canonical Wnt Signaling and N-Cadherin Related β-Catenin Signaling Play a Role in Mechanically Induced Osteogenic Cell Fate [J].
Arnsdorf, Emily J. ;
Tummala, Padmaja ;
Jacobs, Christopher R. .
PLOS ONE, 2009, 4 (04)
[8]
Design of a flow perfusion bioreactor system for bone tissue-engineering applications [J].
Bancroft, GN ;
Sikavitsas, VI ;
Mikos, AG .
TISSUE ENGINEERING, 2003, 9 (03) :549-554
[9]
Fluid flow increases mineralized matrix deposition in 3D perfusion culture of marrow stromal osteloblasts in a dose-dependent manner [J].
Bancroft, GN ;
Sikavitsast, VI ;
van den Dolder, J ;
Sheffield, TL ;
Ambrose, CG ;
Jansen, JA ;
Mikos, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12600-12605
[10]
Long term culture of mesenchymal stem cells in hypoxia promotes a genetic program maintaining their undifferentiated and multipotent status [J].
Basciano, Leticia ;
Nemos, Christophe ;
Foliguet, Bernard ;
de Isla, Natalia ;
de Carvalho, Marcelo ;
Nguyen Tran ;
Dalloul, Ali .
BMC CELL BIOLOGY, 2011, 12