Distribution, gene expression, and functional role of EphA4 during ossification

被引:28
作者
Kuroda, Chisa [1 ,2 ]
Kubota, Satoshi [1 ]
Kawata, Kazumi [1 ]
Aoyama, Eriko [3 ]
Sumiyoshi, Kumi [1 ]
Oka, Morihiko [2 ]
Inoue, Miho [3 ]
Minagi, Shogo [3 ]
Takigawa, Masaharu [1 ,3 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Biochem & Mol Dent, Okayama 7008525, Japan
[2] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Occlusal & Oral Funct Rehabil, Sch Dent, Okayama 7008525, Japan
[3] Okayama Univ, Sch Dent, Biodent Res Ctr, Okayama 7008525, Japan
基金
日本学术振兴会;
关键词
EphA4; Eph family; calcification; chondrocyte; osteoblast;
D O I
10.1016/j.bbrc.2008.06.089
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
EphA4 receptor tyrosine kinase has been shown to be critically involved in neural tissue development. Here, we found EphA4 was also distributed among hypertrophic chondrocytes and osteoblasts in the growth plate of developing mouse long bones. In vitro evaluation revealed that ephA4 expression was elevated Upon hypertrophic differentiation of chondrocytes and that markedly stronger expression was observed in osteoblastic SaOS-2 than chondrocytic HCS-2/8 cells. Of note, RNAi-mediated silencing of ephA4 in SaOS-2 cells resulted in the repression of osteocalcin gene expression and alkaline phosphatase activity. Interestingly, confocal laser-scanning Microscopic analysis revealed the presence of EphA4 molecules in the nucleus as well as on the surface of SaOS-2 cells. These findings are the first indication of a critical role of EphA4 in ossification, especially at the final stage in which osteoblasts and hypertrophic chondrocytes play major roles. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:22 / 27
页数:6
相关论文
共 26 条
[1]
[Anonymous], 1997, Cell, V90, P403
[2]
BESSEY OA, 1946, J BIOL CHEM, V164, P321
[3]
EphA4 (Sek1) receptor tyrosine kinase is required for the development of the corticospinal tract [J].
Dottori, M ;
Hartley, L ;
Galea, M ;
Paxinos, G ;
Polizzotto, M ;
Kilpatrick, T ;
Bartlett, PF ;
Murphy, M ;
Köntgen, F ;
Boyd, AW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13248-13253
[4]
The ephrins and Eph receptors in neural development [J].
Flanagan, JG ;
Vanderhaeghen, P .
ANNUAL REVIEW OF NEUROSCIENCE, 1998, 21 :309-345
[5]
Eph receptors and ligands comprise two major specificity subclasses and are reciprocally compartmentalized during embryogenesis [J].
Gale, NW ;
Holland, SJ ;
Valenzuela, DM ;
Flenniken, A ;
Pan, L ;
Ryan, TE ;
Henkemeyer, M ;
Strebhardt, K ;
Hirai, H ;
Wilkinson, DG ;
Pawson, T ;
Davis, S ;
Yancopoulos, GD .
NEURON, 1996, 17 (01) :9-19
[6]
Growth factors acting via endothelial cell-specific receptor tyrosine kinases: VEGFs, angiopoietins, and ephrins in vascular development [J].
Gale, NW ;
Yancopoulos, GD .
GENES & DEVELOPMENT, 1999, 13 (09) :1055-1066
[7]
Rac-GAP α-chimerin regulates motor-circuit formation as a key mediator of EphrinB3/EphA4 forward signaling [J].
Iwasato, Takuji ;
Katoh, Hironori ;
Nishimaru, Hiroshi ;
Ishikawa, Yukio ;
Inoue, Haruhisa ;
Saito, Yoshikazu M. ;
Ando, Reiko ;
Iwama, Mizuho ;
Takahashi, Ryosuke ;
Negishi, Manabu ;
Itohara, Shigeyoshi .
CELL, 2007, 130 (04) :742-753
[8]
Possible role of LRP1, a CCN2 receptor, in chondrocytes [J].
Kawata, Kazumi ;
Eguchi, Takanori ;
Kubota, Satoshi ;
Kawaki, Harumi ;
Oka, Morihiko ;
Minagi, Shogo ;
Takigawa, Masaharu .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 345 (02) :552-559
[9]
Novel mode of processing and secretion of connective tissue growth factor/ecogenin (CTGF/Hcs24) in chondrocytic HCS-2/8 cells [J].
Kubota, S ;
Eguchi, T ;
Shimo, T ;
Nishida, T ;
Hattori, T ;
Kondo, S ;
Nakanishi, T ;
Takigawa, M .
BONE, 2001, 29 (02) :155-161
[10]
CCN family proteins and angiogenesis: From embryo to adulthood [J].
Kubota S. ;
Takigawa M. .
Angiogenesis, 2007, 10 (1) :1-11