Mesenchymal Stem Cell Stimulation of Tissue Growth Depends on Differentiation State

被引:22
作者
Rothenberg, Ashley R. [1 ]
Ouyang, Lee [1 ]
Elisseeff, Jennifer H. [1 ]
机构
[1] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21218 USA
基金
美国国家卫生研究院;
关键词
MARROW STROMAL CELLS; IN-VITRO; OSTEOGENIC DIFFERENTIATION; BONE-MARROW; MORPHOGENETIC SIGNALS; ARTICULAR-CARTILAGE; ZONAL ORGANIZATION; SUBCHONDRAL BONE; CHONDROCYTES; EXPRESSION;
D O I
10.1089/scd.2010.0097
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The osteochondral microenvironment involves a complex milieu of cues that facilitate proper tissue development, homeostasis, and repair. This environment is disrupted in disease states such as osteoarthritis. Mesenchymal stem cells (MSCs) are under clinical investigation for the treatment of osteoarthritis given their capacity to differentiate into chondrocytes as well as to secrete a wide array of biologically active factors that support cell proliferation and tissue formation. In fact, the therapeutic action of these cells in many clinical applications is now thought to be at least partially dependent on their secretory capacity. Previous work demonstrated that MSCs were capable of stimulating chondrocyte growth and tissue production, whereas tissue-derived osteoblasts were not stimulatory. This study investigated the stimulatory capacity of MSCs during osteogenesis and the impact of MSC phenotype on cartilage stimulation. Cell interactions were examined in 3 coculture systems to confirm that trends were not dependent on material: traditional cell culture insert coculture, bilayered poly(ethylene glycol) gels, and a scaffold comprised of a layer of poly(ethylene glycol) polymerized onto a poly(lactic-co-glycolic) acid-based scaffold. Results demonstrated that MSCs predifferentiated toward an osteogenic phenotype for 3 days exhibited enhanced stimulation of chondrocyte extracellular matrix production, whereas longer periods of predifferentiation decreased the magnitude of observed stimulation. Further, tissue formation by the MSCs themselves showed greater dependence on the coculture system than the presence of other cells or length of predifferentiation.
引用
收藏
页码:405 / 414
页数:10
相关论文
共 45 条
[31]   Repair of large bone defects with the use of autologous bone marrow stromal cells [J].
Quarto, R ;
Mastrogiacomo, M ;
Cancedda, R ;
Kutepov, SM ;
Mukhachev, V ;
Lavroukov, A ;
Kon, E ;
Marcacci, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (05) :385-386
[32]   Enhanced expression of interleukin-6, matrix metalloproteinase-13, and receptor activator of NF-κB ligand in cells derived from osteoarthritic subchondral bone [J].
Sakao, Kei ;
Takahashi, Kenji A. ;
Mazda, Osam ;
Arai, Yuji ;
Tonomura, Hitoshi ;
Inoue, Atsuo ;
Saito, Masazumi ;
Fujioka, Mikihiro ;
Takamiya, Hisatake ;
Imanishi, Jiro ;
Kubo, Toshikazu .
JOURNAL OF ORTHOPAEDIC SCIENCE, 2008, 13 (03) :202-210
[33]   In vitro secreting profile of human mesenchymal stem cells [J].
Schinkothe, Timo ;
Bloch, Wilhelm ;
Schmidt, Annette .
STEM CELLS AND DEVELOPMENT, 2008, 17 (01) :199-205
[34]   Tissue engineering of a small hand phalanx with a porously casted polylactic acid-polyglycolic acid copolymer [J].
Sedrakyan, Sargis ;
Zhou, Zhao Yi ;
Perin, Laura ;
Leach, Kent ;
Mooney, David ;
Kim, Tae Ho .
TISSUE ENGINEERING, 2006, 12 (09) :2675-2683
[35]   Designing zonal organization into tissue-engineered cartilage [J].
Sharma, Blanka ;
Williams, Christopher G. ;
Kim, Tae Kyun ;
Sun, Dongning ;
Malik, Athar ;
Khan, Mehnaz ;
Leong, Kam ;
Elisseeff, Jennifer H. .
TISSUE ENGINEERING, 2007, 13 (02) :405-414
[36]  
Tetlow LC, 2001, ARTHRITIS RHEUM-US, V44, P585, DOI 10.1002/1529-0131(200103)44:3<585::AID-ANR107>3.3.CO
[37]  
2-3
[38]  
Thomsen J. S., 2008, Journal of Musculoskeletal & Neuronal Interactions, V8, P22
[39]   Human mesenchymal progenitor cell-based tissue engineering of a single-unit osteochondral construct [J].
Tuli, R ;
Nandi, S ;
Li, WJ ;
Tuli, S ;
Huang, XX ;
Manner, PA ;
Laquerriere, P ;
Nöth, U ;
Hall, DJ ;
Tuan, RS .
TISSUE ENGINEERING, 2004, 10 (7-8) :1169-1179
[40]   Bioresponsive phosphoester hydrogels for bone tissue engineering [J].
Wang, DA ;
Williams, CG ;
Yang, F ;
Cher, N ;
Lee, H ;
Elisseeff, JH .
TISSUE ENGINEERING, 2005, 11 (1-2) :201-213