Activation of the extracellular signal-regulated kinases 1 and 2 (ERK1/2) is needed for the TGFβ-induced chondrogenic and osteogenic differentiation of mesenchymal stem cells

被引:45
作者
Arita, Nestor A. [2 ]
Pelaez, Daniel [1 ,2 ]
Cheung, Herman S. [1 ,2 ]
机构
[1] Miami VA Med Ctr, Res Serv, Miami, FL 33125 USA
[2] Univ Miami, Coll Engn, Dept Biomed Engn, Coral Gables, FL 33124 USA
关键词
Mesenchymal stem cells; Chondrogenesis; Osteogenesis; MAPK; PATHWAYS; P38;
D O I
10.1016/j.bbrc.2011.01.068
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
The role of the extracellular signal-regulated kinase 1/2 (ERK1/2) pathway on the osteogenesis of progenitor and stem cells has received a lot of attention due to conflicting results in the literature. ERK1/2 has been reported to be both activating and inhibitory to the osteogenesis of different cell types under varying culture conditions. This study focused specifically on the role of ERK1/2 on the chondrogenesis and osteogenesis of mesenchymal stern cells (MSC) induced by cytokine exposure. Bone marrow-derived MSC were cultured in three-dimensional fibrin gel scaffolds and stimulated down the chondrogenic and osteogenic programs by addition of TGF-beta 3 to and osteogenic buffer media. Cells were cultured under control conditions (no cytokine supplementation), treated with TGF-beta 3 or treated with PD98059 + TGF-beta 3 for 7 days. RT-PCR results show that addition of TGF-beta 3 significantly upregulates the phosphorylation of ERK1/2 and induces the cells down the chondrogenic and osteogenic pathways (as demonstrated by the significant upregulation of aggrecan, sox9, collagen types 1 & 2 gene expressions). Inhibition of ERK1/2 phosphorylation with PD98059 led to the abolishment of the upregulation of chondrogenic and osteogenic-specific gene expressions. These results demonstrate that ERK1/2 is needed for the chondrogenic and osteogenic differentiation of MSC as induced by TGF-beta 3 supplementation. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:564 / 569
页数:6
相关论文
共 30 条
[1]
Therapeutic Potential of the Immunomodulatory Activities of Adult Mesenchymal Stem Cells [J].
Aronin, Caren E. Petrie ;
Tuan, Rocky S. .
BIRTH DEFECTS RESEARCH PART C-EMBRYO TODAY-REVIEWS, 2010, 90 (01) :67-74
[2]
The Regulation of Differentiation in Mesenchymal Stem Cells [J].
Augello, Andrea ;
De Bari, Cosimo .
HUMAN GENE THERAPY, 2010, 21 (10) :1226-1238
[3]
MEK-ERK signaling plays diverse roles in the regulation of facial chondrogenesis [J].
Bobick, BE ;
Kulyk, WM .
EXPERIMENTAL CELL RESEARCH, 2006, 312 (07) :1079-1092
[4]
The association of human mesenchymal stem cells with BMP-7 improves bone regeneration of critical-size segmental bone defects in athymic rats [J].
Burastero, Giorgio ;
Scarfi, Sonia ;
Ferraris, Chiara ;
Fresia, Chiara ;
Sessarego, Nadia ;
Fruscione, Floriana ;
Monetti, Francesco ;
Scarfo, Francesca ;
Schupbach, Peter ;
Podesta, Marina ;
Grappiolo, Guido ;
Zocchi, Elena .
BONE, 2010, 47 (01) :117-126
[5]
Involvement of Gas7 along the ERK1/2 MAP kinase and SOX9 pathway in chondrogenesis of human marrow-derived mesenchymal stem cells [J].
Chang, Y. ;
Ueng, S. W. N. ;
Lin-Chao, S. ;
Chao, C. C. -K. .
OSTEOARTHRITIS AND CARTILAGE, 2008, 16 (11) :1403-1412
[6]
Mesenchymal stem cells as a potential pool for cartilage tissue engineering [J].
Csaki, C. ;
Schneider, P. R. A. ;
Shakibaei, M. .
ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER, 2008, 190 (05) :395-412
[7]
Mechanisms of bone repair and regeneration [J].
Deschaseaux, Frederic ;
Sensebe, Luc ;
Heymann, Dominique .
TRENDS IN MOLECULAR MEDICINE, 2009, 15 (09) :417-429
[8]
FRIEDENSTEIN AJ, 1976, EXP HEMATOL, V4, P267
[9]
Im DD, 2010, TISSUE ENG PT A, V16, P3485, DOI [10.1089/ten.tea.2010.0222, 10.1089/ten.TEA.2010.0222]
[10]
Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases [J].
Johnson, GL ;
Lapadat, R .
SCIENCE, 2002, 298 (5600) :1911-1912