Immunohistochemical and biochemical analyses of GD3, GT1b, and GQ1b gangliosides during neural differentiation of P19 EC cells

被引:11
作者
Osanai, T
Kotani, M
Yuen, CT
Kato, H
Sanai, Y
Takeda, S
机构
[1] Tokyo Metropolitan Org Med Res, Tokyo Metropolitan Inst Med Sci, RINSHOKEN, Dept Biochem Cell Res,Bunkyo Ku, Tokyo 1138613, Japan
[2] Tokyo Metropolitan Org Med Res, Tokyo Metropolitan Inst Med Sci, RINSHOKEN, Dept Clin Genet,Bunkyo Ku, Tokyo 1138613, Japan
[3] Natl Inst Biol Stand & Controls, Mol Struct Lab, Potters Bar EN6 3QG, Herts, England
[4] Leica Microsyst KK, Shinagawa Ku, Tokyo 1410032, Japan
[5] Niigata Neurosurg Hosp, Niigata 9501101, Japan
关键词
ganglioside; sialyltransferase; retinoic acid; neural cell differentiation; confocal laser scanning microscopy;
D O I
10.1016/S0014-5793(03)00083-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In an earlier study, we showed that expressions of GD3, GT1b, and GQ1b gangliosides in P19 embryonic carcinoma (EQ cells were enhanced during their neural differentiation induced by retinoic acid. We now further demonstrated that this increase of the b-series gangliosides is due to an increase in their corresponding synthases (sialyltransferase-II, -IV, and -V) in the Golgi. Of the three gangliosides studied, GQ1b appeared to be the best candidate for monitoring such differentiation process. We also used fluorescence-labeled monoclonal antibodies and confocal fluorescence microscopy to obtain direct visual information about the relationship of gangliosides and neural specific proteins in neuron development. Again, GQ1b is the most interesting as it localizes with synaptophysin and neural cell adhesion molecules (NCAMs) on synaptic boutons or dendritic spines in RA-induced neurons (R/N). This suggests that GQ1b could be used as a marker for synapse formation during construction of the neural network. (C) 2003 Federation of European Biochemical Societies. PubUshed by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:73 / 78
页数:6
相关论文
共 24 条
[1]  
Brown RE, 1998, J CELL SCI, V111, P1
[2]  
Finley MFA, 1996, J NEUROSCI, V16, P1056
[3]   Ganglioside synthesis during the development of neuronal polarity - Major changes occur during axonogenesis and axon elongation, but not during dendrite growth or synaptogenesis [J].
Hirschberg, K ;
Zisling, R ;
vanEchtenDeckert, G ;
Futerman, AH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (25) :14876-14882
[4]   UP-REGULATION OF EMBRYONIC NCAM IN AN EC CELL-LINE BY RETINOIC ACID [J].
HUSMANN, M ;
GORGEN, I ;
WEISGERBER, C ;
BITTERSUERMANN, D .
DEVELOPMENTAL BIOLOGY, 1989, 136 (01) :194-200
[5]   SYNAPSIN-I (PROTEIN-I), A NERVE TERMINAL-SPECIFIC PHOSPHOPROTEIN .3. ITS ASSOCIATION WITH SYNAPTIC VESICLES STUDIED IN A HIGHLY PURIFIED SYNAPTIC VESICLE PREPARATION [J].
HUTTNER, WB ;
SCHIEBLER, W ;
GREENGARD, P ;
DECAMILLI, P .
JOURNAL OF CELL BIOLOGY, 1983, 96 (05) :1374-1388
[6]   SUBSTRATE-SPECIFICITY OF ALPHA-2-]3-SIALYLTRANSFERASES IN GANGLIOSIDE BIOSYNTHESIS OF RAT-LIVER GOLGI [J].
IBER, H ;
VANECHTEN, G ;
SANDHOFF, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1991, 195 (01) :115-120
[7]   FRACTIONATION OF PRIMARY CULTURED CEREBELLAR NEURONS - DISTRIBUTION OF SIALYLTRANSFERASES INVOLVED IN GANGLIOSIDE BIOSYNTHESIS [J].
IBER, H ;
VANECHTEN, G ;
SANDHOFF, K .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (04) :1533-1537
[8]   THE BETA-1,4-GALACTOSYLTRANSFERASE GENE IS POSTTRANSCRIPTIONALLY REGULATED DURING DIFFERENTIATION OF MOUSE F9 TERATOCARCINOMA CELLS [J].
KUDO, T ;
NARIMATSU, H .
GLYCOBIOLOGY, 1995, 5 (04) :397-405
[9]  
LEVINE JM, 1986, J NEUROSCI, V6, P3374
[10]  
Liour SS, 2000, J NEUROSCI RES, V62, P363, DOI 10.1002/1097-4547(20001101)62:3<363::AID-JNR6>3.3.CO