Specificity of carbohydrate structures of gangliosides in the activity to regenerate the rat axotomized hypoglossal nerve

被引:15
作者
Itoh, M
Fukumoto, S
Iwamoto, T
Mizuno, A
Rokutanda, A
Ishida, HK
Kiso, M
Furukawa, K [1 ]
机构
[1] Nagoya Univ, Sch Med, Dept Biochem 2, Nagoya, Aichi 4660065, Japan
[2] Nagasaki Univ, Sch Dent, Dept Oral & Maxillofacial Surg 1, Nagasaki 8528102, Japan
[3] Nagasaki Univ, Sch Dent, Dept Pediat Dent, Nagasaki 8528102, Japan
[4] Nagasaki Univ, Sch Dent, Dept Oral Anat, Nagasaki 8528102, Japan
[5] Gifu Univ, Fac Agr, Dept Appl Bioorgan Chem, Gifu 5011193, Japan
关键词
gangliosides; hypoglossal nerve; nerve regeneration; ceramide; carbohydrate;
D O I
10.1093/glycob/11.2.125
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
We previously reported that a ganglioside mixture from bovine brain could prevent neuronal death and promote regeneration in rats with hypoglossal nerve resection. In the present study, we have compared the neurotrophic effects of various glycosphingolipids including lactosylceramide, The findings revealed that GT1b had the activity of neuronal death prevention equivalent to a ganglioside mixture or autograft, while other glycolipids exhibited about 60% activity. However, the capability to promote the regeneration varied among glycolipids, that is, GT1b (86%), GD1b (55%), GD1a (35%), GQ1b (34%), GM1 (20%), lactosyl-ceramide (17%) in the number of horseradish peroxidase-positive neurons as an indicator of regeneration. The experiments with oligosaccharides of GT1b or GD1b and ceramide showed that the carbohydrate moiety mainly exerts neurotrophic effects. These findings suggested that fine structures of carbohydrate moiety in gangliosides are critical in the regenerative activity in this hypoglossal nerve regeneration system.
引用
收藏
页码:125 / 130
页数:6
相关论文
共 31 条
[1]   GANGLIOSIDES POTENTIATE INVIVO AND INVITRO EFFECTS OF NERVE GROWTH-FACTOR ON CENTRAL CHOLINERGIC NEURONS [J].
CUELLO, AC ;
GAROFALO, L ;
KENIGSBERG, RL ;
MAYSINGER, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (06) :2056-2060
[2]   GANGLIOSIDES PREVENT GLUTAMATE AND KAINATE NEUROTOXICITY IN PRIMARY NEURONAL CULTURES OF NEONATAL RAT CEREBELLUM AND CORTEX [J].
FAVARON, M ;
MANEV, H ;
ALHO, H ;
BERTOLINO, M ;
FERRET, B ;
GUIDOTTI, A ;
COSTA, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (19) :7351-7355
[3]   GANGLIOSIDES ENHANCE NEURITE OUTGROWTH IN PC12 CELLS [J].
FERRARI, G ;
FABRIS, M ;
GORIO, A .
DEVELOPMENTAL BRAIN RESEARCH, 1983, 8 (2-3) :215-221
[4]   PREVENTION OF APOPTOTIC NEURONAL DEATH BY G(M1) GANGLIOSIDE - INVOLVEMENT OF TRK NEUROTROPHIN RECEPTORS [J].
FERRARI, G ;
ANDERSON, BL ;
STEPHENS, RM ;
KAPLAN, DR ;
GREENE, LA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (07) :3074-3080
[5]   CHARACTERIZATION OF GLIAL TRKB RECEPTORS - DIFFERENTIAL RESPONSE TO INJURY IN THE CENTRAL AND PERIPHERAL NERVOUS SYSTEMS [J].
FRISEN, J ;
VERGE, VMK ;
FRIED, K ;
RISLING, M ;
PERSSON, H ;
TROTTER, J ;
HOKFELT, T ;
LINDHOLM, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :4971-4975
[6]   GD3 synthase gene expression in PC12 cells results in the continuous activation of TrkA and ERK1/2 and enhanced proliferation [J].
Fukumoto, S ;
Mutoh, T ;
Hasegawa, T ;
Miyazaki, H ;
Okada, M ;
Goto, G ;
Furukawa, K ;
Urano, T ;
Furukawa, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (08) :5832-5838
[7]   DIFFERENTIAL EXPRESSION OF MESSENGER-RNAS FOR NEUROTROPHINS AND THEIR RECEPTORS AFTER AXOTOMY OF THE SCIATIC-NERVE [J].
FUNAKOSHI, H ;
FRISEN, J ;
BARBANY, G ;
TIMMUSK, T ;
ZACHRISSON, O ;
VERGE, VMK ;
PERSSON, H .
JOURNAL OF CELL BIOLOGY, 1993, 123 (02) :455-465
[8]  
HAKOMORI SI, 1990, J BIOL CHEM, V265, P18713
[9]   TOTAL SYNTHESIS OF GANGLIOSIDE GQ1B AND THE RELATED POLYSIALOGANGLIOSIDES [J].
ISHIDA, HK ;
ISHIDA, H ;
KISO, M ;
HASEGAWA, A .
TETRAHEDRON-ASYMMETRY, 1994, 5 (12) :2493-2512
[10]   Prevention of the death of the rat axotomized hypoglossal nerve and promotion of its regeneration by bovine brain gangliosides [J].
Itoh, M ;
Fukumoto, S ;
Baba, N ;
Kuga, Y ;
Mizuno, A ;
Furukawa, K .
GLYCOBIOLOGY, 1999, 9 (11) :1247-1252