Role of c-jun N-terminal kinase in the PDGF-induced proliferation and migration of human adipose tissue-derived mesenchymal stem cells

被引:98
作者
Kang, YJ [1 ]
Jeon, ES [1 ]
Song, HY [1 ]
Woo, JS [1 ]
Jung, JS [1 ]
Kim, YK [1 ]
Kim, JH [1 ]
机构
[1] Pusan Natl Univ, Coll Med, Med Res Inst, Dept Physiol, Pusan 602739, South Korea
关键词
mesenchymal stem cells; proliferation; migration; PDGF; JNK;
D O I
10.1002/jcb.20499
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Platelet-derived growth factor (PDGF) is a critical regulator of proliferation and migration for mesenchymal type cells. In this study, we examined the role of mitogen-activated protein (MAP) kinases in the PDGF-BB-incluced proliferation and migration of human adipose tissue-derived mesenchymal stem cells (hATSCs). The PDGF-induced proliferation was prevented by a pretreatment with the c-Jun N-terminal kinase (JNK) inhibitor, SP600125. However, it was not prevented by a pretreatment with a p38 MAP kinase inhibitor, SB202190, and a specific inhibitor of the upstream kinase of extracellular signal-regulated kinase (ERK1/2), U0126. Treatment with PDGF induced the activation of JNK and ERK in hATSCs, and pretreatment with SP600125 specifically inhibited the PDGF-induced activation of JNK. Treatment with PDGF induced the cell cycle transition from the G0/G1 phase to the S phase, the elevated expression of cyclin D1, and the phosphorylation of Rb, which were prevented by a pretreatment with SP600125. In addition, the PDGF-induced migration of hATSCs was completely blocked by a pretreatment with SP600125, but not with U0126 and SB202190. These results suggest that JNK protein kinase plays a key role in the PDGF-induced proliferation and migration of mesenchymal stem cells.
引用
收藏
页码:1135 / 1145
页数:11
相关论文
共 37 条
[1]
ALLEY MC, 1988, CANCER RES, V48, P589
[2]
[Anonymous], 1998, Biochim. Biophys. Acta
[3]
Mesenchymal stem cells: clinical applications and biological characterization [J].
Barry, FP ;
Murphy, JM .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2004, 36 (04) :568-584
[4]
MESENCHYMAL STEM-CELLS [J].
CAPLAN, AI .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1991, 9 (05) :641-650
[5]
Mammalian MAP kinase signalling cascades [J].
Chang, LF ;
Karin, M .
NATURE, 2001, 410 (6824) :37-40
[6]
Signal transduction by the JNK group of MAP kinases [J].
Davis, RJ .
CELL, 2000, 103 (02) :239-252
[7]
Inhibition of cell proliferation and cell cycle progression by specific inhibition of basal JNK activity - Evidence that mitotic Bcl-2 phosphorylation is JNK-independent [J].
Du, LH ;
Lyle, CS ;
Obey, TB ;
Gaarde, WA ;
Muir, JA ;
Bennett, BL ;
Chambers, TC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (12) :11957-11966
[8]
Chondrogenic potential of adipose tissue-derived stromal cells in vitro and in vivo [J].
Erickson, GR ;
Gimble, JM ;
Franklin, DM ;
Rice, HE ;
Awad, H ;
Guilak, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 290 (02) :763-769
[9]
BMP-2, BMP-4, and PDGF-bb stimulate chemotactic migration of primary human mesenchymal progenitor cells [J].
Fiedler, J ;
Röderer, G ;
Günther, KP ;
Brenner, RE .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2002, 87 (03) :305-312
[10]
Extracellular matrix mineralization and osteoblast gene expression by human adipose tissue-derived stromal cells [J].
Halvorsen, YDC ;
Franklin, D ;
Bond, AL ;
Hitt, DC ;
Auchter, C ;
Boskey, AL ;
Paschalis, EP ;
Wilkison, WO ;
Gimble, JM .
TISSUE ENGINEERING, 2001, 7 (06) :729-741