MicroRNA-140 Expression During Chondrogenic Differentiation of Equine Cord Blood-Derived Mesenchymal Stromal Cells

被引:43
作者
Buechli, Midori E. [1 ]
LaMarre, Jonathan [1 ]
Koch, Thomas G. [1 ,2 ]
机构
[1] Univ Guelph, Ontario Vet Coll, Dept Biomed Sci, Guelph, ON N1G 2W1, Canada
[2] Aarhus Univ, Dept Clin Med, Orthopaed Res Lab, Aarhus, Denmark
基金
加拿大自然科学与工程研究理事会;
关键词
COLLAGEN-INDUCED ARTHRITIS; BONE-MARROW; STEM-CELLS; IN-VITRO; CHONDROCYTE PROLIFERATION; HUMAN FIBROBLASTS; ADIPOSE-TISSUE; CARTILAGE; TARGETS; GROWTH;
D O I
10.1089/scd.2012.0411
中图分类号
Q813 [细胞工程];
学科分类号
摘要
MicroRNAs are a class of short noncoding RNAs that are involved in various biological processes, including differentiation. MicroRNA-140 (miR-140) has been identified as a cartilage-specific microRNA with several targets involved in cartilage development and homeostasis. The aim of this study was to investigate the expression of miR-140 during chondrogenic differentiation of equine cord blood-derived mesenchymal stromal cells (eCB-MSCs). We demonstrate both that miR-140 is highly expressed in normal equine articular cartilage and that eCB-MSCs express significantly higher levels of this microRNA after 14 days of chondrogenic differentiation. Furthermore, miR-140 expression closely paralleled that of the cartilage-specific transcription factor Sox9, suggesting that miR-140 may be under the transcriptional regulation of Sox9 in these cells. The expression patterns of miR-140 targets the chemokine (CXC motif) ligand 12 (CXCL12), A disintegrin and metalloproteinase with thrombosponin motifs (ADAMTS)-5 and insulin growth factor binding protein 5 (IGFBP5) were also determined; however, only CXCL12 and ADAMTS-5 were repressed while miR-140 expression was upregulated. Together, these studies suggest that miR-140 is an important regulator of cartilage development and homeostasis in eCB-MSCs that may act, in part, through the regulation of CXCL12 and ADAMTS-5.
引用
收藏
页码:1288 / 1296
页数:9
相关论文
共 49 条
[1]   Direct Reprogramming of Adult Human Fibroblasts to Functional Neurons under Defined Conditions [J].
Ambasudhan, Rajesh ;
Talantova, Maria ;
Coleman, Ronald ;
Yuan, Xu ;
Zhu, Saiyong ;
Lipton, Stuart A. ;
Ding, Sheng .
CELL STEM CELL, 2011, 9 (02) :113-118
[2]  
Bailey C J, 1999, Vet Rec, V145, P487
[3]   Chondrogenic potential of mesenchymal stromal cells derived from equine bone marrow and umbilical cord blood [J].
Berg, L. C. ;
Koch, T. G. ;
Heerkens, T. ;
Besonov, K. ;
Thomsen, P. D. ;
Betts, D. H. .
VETERINARY AND COMPARATIVE ORTHOPAEDICS AND TRAUMATOLOGY, 2009, 22 (05) :363-370
[4]   MicroRNAs modulate hematopoietic lineage differentiation [J].
Chen, CZ ;
Li, L ;
Lodish, HF ;
Bartel, DP .
SCIENCE, 2004, 303 (5654) :83-86
[5]   Cloning and expression of ADAM-related metalloproteases in equine laminitis [J].
Coyne, Michael J. ;
Cousin, Helene ;
Loftus, John P. ;
Johnson, Philip J. ;
Belknap, James K. ;
Gradil, Carlos M. ;
Black, Samuel J. ;
Alfandari, Dominique .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2009, 129 (3-4) :231-241
[6]   Expression of CXC chemokines and their receptors is modulated during chondrogenic differentiation of human mesenchymal stem cells grown in three-dimensional scaffold: Evidence in native cartilage [J].
Cristino, Sandra ;
Piacentini, Anna ;
Manferdini, Cristina ;
Codeluppi, Katia ;
Grassi, Francesco ;
Facchini, Andrea ;
Lisignoli, Gina .
TISSUE ENGINEERING PART A, 2008, 14 (01) :97-105
[7]   Smad Proteins Bind a Conserved RNA Sequence to Promote MicroRNA Maturation by Drosha [J].
Davis, Brandi N. ;
Hilyard, Aaron C. ;
Nguyen, Peter H. ;
Lagna, Giorgio ;
Hata, Akiko .
MOLECULAR CELL, 2010, 39 (03) :373-384
[8]   Pro-inflammatory properties of stromal cell-derived factor-1 (CXCL12) in collagen-induced arthritis [J].
De Klerck, B ;
Geboes, L ;
Hatse, S ;
Kelchtermans, H ;
Meyvis, Y ;
Vermeire, K ;
Bridger, G ;
Billiau, A ;
Schols, D ;
Matthys, P .
ARTHRITIS RESEARCH & THERAPY, 2005, 7 (06) :R1208-R1220
[9]   microPrimer: The biogenesis and function of microRNA [J].
Du, TT ;
Zamore, PD .
DEVELOPMENT, 2005, 132 (21) :4645-4652
[10]   Deletion of active ADAMTS5 prevents cartilage degradation in a murine model of osteoarthritis [J].
Glasson, SS ;
Askew, R ;
Sheppard, B ;
Carito, B ;
Blanchet, T ;
Ma, HL ;
Flannery, CR ;
Peluso, D ;
Kanki, K ;
Yang, ZY ;
Majumdar, MK ;
Morris, EA .
NATURE, 2005, 434 (7033) :644-648