Signalling molecules and growth factors for tissue engineering of cartilage - What can we learn from the growth plate?

被引:29
作者
Brochhausen, Christoph [1 ]
Lehmann, Meike [1 ]
Halstenberg, Sven [1 ]
Meurer, Andrea [2 ]
Klaus, Guenter [3 ]
Kirkpatrick, C. James [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, REPAIR Lab, Inst Pathol, D-55101 Mainz, Germany
[2] Goethe Univ Frankfurt, Orthopaed Clin, D-60590 Frankfurt, Germany
[3] Univ Marburg, Dept Paediat, D-35043 Marburg, Germany
关键词
growth plate; signalling molecules; growth factors; tissue engineering; development; articular cartilage; regenerative medicine; LONGITUDINAL BONE-GROWTH; ACTIVATING TRANSCRIPTION FACTOR-2; CHONDROCYTE DIFFERENTIATION; GENE-EXPRESSION; IN-VITRO; HYPERTROPHIC CHONDROCYTES; DEVELOPMENTAL REGULATION; EPIPHYSEAL PLATE; EAR CHONDROCYTES; INDIAN HEDGEHOG;
D O I
10.1002/term.192
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Modern tissue engineering concepts integrate cells, scaffolds, signalling molecules and growth factors. For the purposes of regenerative medicine, fetal development is of great interest because it is widely accepted that regeneration recapitulates in part developmental processes. In tissue engineering of cartilage the growth plate of the long bone represents an interesting, well-organized developmental structure with a spatial distribution of chondrocytes in different proliferation and differentiation stages, embedded in a scaffold of extracellular matrix components. The proliferation and differentiation of these chondrocytes is regulated by various hormonal and paracrine factors. Thus, members of the TGF beta superfamily, the parathyroid hormone-related peptide-Indian hedgehog loop and a number of transcription factors, such as Sox and Runx, are involved in the regulation of chondrocyte proliferation and differentiation. Furthermore, adhesion molecules, homeobox genes, metalloproteinases and prostaglandins play a role in the complex regulation mechanisms. The present paper summarizes the morphological organization of the growth plate and provides a short but not exhaustive overview of the regulation of growth plate development, giving interesting insights for tissue engineering of cartilage. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:416 / 429
页数:14
相关论文
共 146 条
[1]   The role of the resting zone in growth plate chondrogenesis [J].
Abad, V ;
Meyers, JL ;
Weise, M ;
Gafni, RI ;
Barnes, KM ;
Nilsson, O ;
Bacher, JD ;
Baron, J .
ENDOCRINOLOGY, 2002, 143 (05) :1851-1857
[2]  
Aberle H, 1996, J CELL BIOCHEM, V61, P514, DOI 10.1002/(SICI)1097-4644(19960616)61:4<514::AID-JCB4>3.0.CO
[3]  
2-R
[4]   Growth plate cartilage as developmental model in osteoarthritis research - Potentials and limitations [J].
Aigner, T. ;
Gerwin, N. .
CURRENT DRUG TARGETS, 2007, 8 (02) :377-385
[5]   Functional genomics of osteoarthritis - On the way to evaluate disease hypotheses [J].
Aigner, T ;
Bartnik, E ;
Sohler, F ;
Zimmer, R .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2004, (427) :S138-S143
[6]   Functional genomics of osteoarthritis [J].
Aigner, T ;
Bartnik, E ;
Zien, A ;
Zimmer, R .
PHARMACOGENOMICS, 2002, 3 (05) :635-650
[7]   MATRIX METALLOPROTEINASE-2 IS AN INTERSTITIAL COLLAGENASE - INHIBITOR-FREE ENZYME CATALYZES THE CLEAVAGE OF COLLAGEN FIBRILS AND SOLUBLE NATIVE TYPE-I COLLAGEN GENERATING THE SPECIFIC 3/4-LENGTH AND 1/4-LENGTH FRAGMENTS [J].
AIMES, RT ;
QUIGLEY, JP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :5872-5876
[8]   The transcrintion factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6 [J].
Akiyama, H ;
Chaboissier, MC ;
Martin, JF ;
Schedl, A ;
de Crombrugghe, B .
GENES & DEVELOPMENT, 2002, 16 (21) :2813-2828
[9]   Regulation of biomechanical signals by NF-κB transcription factors in chondrocytes [J].
Anghelina, Mirela ;
Sjostrom, Danen ;
Perera, Priyangi ;
Nam, Jin ;
Knobloch, Thomas ;
Agarwal, Sudha .
BIORHEOLOGY, 2008, 45 (3-4) :245-256
[10]   PGE2 signal through EP2 promotes the growth of articular chondrocytes [J].
Aoyama, T ;
Liang, BJ ;
Okamoto, T ;
Matsusaki, T ;
Nishijo, K ;
Ishibe, T ;
Yasura, K ;
Nagayama, S ;
Nakayama, T ;
Nakamura, T ;
Toguchida, J .
JOURNAL OF BONE AND MINERAL RESEARCH, 2005, 20 (03) :377-389