N-acetylglucosaminyltransferase III expression is regulated by cell-cell adhesion via the E-cadherin-catenin-actin complex

被引:30
作者
Akama, Ryota [1 ]
Sato, Yuya [1 ]
Kariya, Yoshinobu [1 ]
Isaji, Tomoya [1 ]
Fukuda, Tomohiko [1 ]
Lu, Lianghao [1 ]
Taniguchi, Naoyuki [2 ]
Ozawa, Masayuki [3 ]
Gu, Jianguo [1 ]
机构
[1] Tohoku Pharmaceut Univ, Div Regulatory Glycobiol, Aoba Ku, Sendai, Miyagi 9818558, Japan
[2] Osaka Univ, Dept Dis Glyc, Inst Microbial Dis, Ctr Adv Sci & Innovat, Osaka, Japan
[3] Kagoshima Univ, Fac Med, Dept Biochem, Kagoshima 890, Japan
基金
日本科学技术振兴机构;
关键词
cell adhesion; E-cadherin; glycosylation; GnT-III; regulation;
D O I
10.1002/pmic.200800038
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recently, our research group investigated the effects of cell-cell interactions on N-linked oligosaccharides (N-glycans). We found that N-acetylglucosaminyltransferase III (GnT-III) activity, and thus, the enzyme product-bisected N-glycans were induced in cells cultured under dense condition in an E-cadherin-dependent manner [26]. To further explore the underlying molecular mechanism, we examined the effects of a-catenin, which is a component of the E-cadherin-catenin complex that can bind to actin cytoskeleton, on the regulation of GnT-III expression in the human colon carcinoma DLD-1 cells. GnT-III activity was not substantially increased in cells cultured under dense conditions, compared with those cultured under sparse conditions. However, restoration of of.-catenin gene to DLD-1 cells resulted in a significant increase in GnT-III activity and in production of the bisected N-glycans, which were detected by E-4-PHA, suggesting that the E-cadherin-catenin complex is required for the induction. Moreover, treatment with cytochalasin D, an inhibitor of F-actin polymerization, completely blocked the upregulation of GnT-III expression in the dense culture. Taken together, these results strongly suggest that GnT-III expression is tightly regulated by cell-cell adhesion via the E-cadherin-catenin complex and actin cytoskeleton formation.
引用
收藏
页码:3221 / 3228
页数:8
相关论文
共 46 条
[1]  
[Anonymous], BIOCH SOC S
[2]  
[Anonymous], BIOCH BIOPHYS ACTA
[3]  
Asada M, 1997, CANCER RES, V57, P1073
[4]   Rac activation upon cell-cell contact formation is dependent on signaling from the epidermal growth factor receptor [J].
Betson, M ;
Lozano, E ;
Zhang, JK ;
Braga, VMM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (40) :36962-36969
[5]  
Dennis JW, 1999, BIOESSAYS, V21, P412, DOI 10.1002/(SICI)1521-1878(199905)21:5<412::AID-BIES8>3.0.CO
[6]  
2-5
[7]  
DWEK RA, 1995, BIOCHEM SOC T, V23, P1
[8]   Roles of mucin-type O-glycans in cell adhesion [J].
Fukuda, M .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2002, 1573 (03) :394-405
[9]  
Granovsky M, 2000, NAT MED, V6, P306
[10]   β1,4-N-Acetylglucosaminyltransferase III down-regulates neurite outgrowth induced by costimulation of epidermal growth factor and integrins through the Ras/ERK signaling pathway in PC12 cells [J].
Gu, JG ;
Zhao, YY ;
Isaji, T ;
Shibukawa, Y ;
Ihara, H ;
Takahashi, M ;
Ikeda, Y ;
Miyoshi, E ;
Honke, K ;
Taniguchi, N .
GLYCOBIOLOGY, 2004, 14 (02) :177-186