 |
Glycolipids are a group of amphopathic molecules
consisting of lipids named ceramide and carbohydrates. They exist
abundantly in the nervous system of vertebrates, but are also
present broadly in other tissues and cells. Depending on the
sugar that attaches to the nonreduced end of lactosylceramide,
Gal-Glc-Cer, three synthetic pathways leading to the formation
of lacto-series (neolacto-series), globo-series , and ganglio-series
have been defined. Above all, the ganglio-series glycolipids
contain many sialic acids , and are designted ganglyosides. They
have been considered to be impotant in the functions of the nervous
system.
A number of functions of gangliosides, such as neurotrophic factor-like
actions, have been reported. However, it was difficult to learn
the actual roles of gangliosides, because many studies were conducted
by the observation of effects of exogenous gangliosides on cells
and tissues. Recently, glycosyltransferase genes have been cloned
and their availability has enabled us to remodel the carbohydrate
structures in the levels of cultured cells and experimental animals,
resulting in the elucidation of novel functions of carbohydrates.
In particular, gene knock-out is expected to be a unique approach
to obtaining definite results, although there are some disadvantages.
Among glycosyltransferase genes responsible for the synthesis
of glycolipids, GM2/GD2 synthase and galactosyltransferase (Gal-Cer
synthase) have been knocked out to date. The former was generated
by our group, and the latter was established by K. Suzuki and
W. Stoffel, independently. In GM2/GD2 synthase knock-out mice,
no morphological changes or apparent abnormal behaviors were
observed. Only significantly lowered nerve conductivity was detected.
These results were much less than expected. One possible explanation
is that the remaining simpler gangliosides may compensate for
the functions of the complex gangliosides. The fact that regeneration
after nerve injury was markedly suppressed and degeneration of
the peripheral nerves took place in the knock-out mice may indicate
that complex gangliosides are critical for the maintenance and
repair of nerve tissue. The Most serious phenotype in the knock-out
mice was male infertility due to spermatogenesis, giving rise
to the idea that gangliosides may be involved in testosterone
transport. Moreover, dysfunctions in T lymphocytes were also
reported. All these results indicate that gangliosides are involved
in the systemic regulatory systems.
In the knock-out mice of Gal-Cer synthase, termor, ataxia, and
deficits in nerve conduction were observed, indicating that galactosylceramide
and its sulfated derivatives are impotant in the maintenance
and stabilization of myelin. Therefore, these mutant mice can
not survive for a long time after birth.
If knock-out mice of other glycosyltransferase genes become available,
the precise roles of the individual carbohydrate structures can
be demonstrated. |
|
|
| References |
(1) |
Takamiya K, Yamamoto A, Furukawa K, Yamashiro S, Shin M,
Okada M, Fukumoto S, Haraguchi M, Takeda N, Fujimura K, Sakae
M, Kishikawa M, Shiku H, Furukawa K, Aizawa S: Mice with disrupted
GM2/GD2 synthase gene lack complex gangliosides but exhibit only
subtle defects in their nervous system. Proc. Natl. Acad. Sci.
USA 93, 10662-10667, 1996. |
|
(2) |
Takamiya K, Yamamoto A, Furukawa K, Zhao J, Yamashiro S,
Okada M, Haraguchi M, Shin M, Kishikawa M, Shiku H, Aizawa S,
Furukawa K: Complex gangliosides are essential in spermatogenesis
of mice : Possible roles in the transport of testosterone. Proc.
Natl. Acad. Sci. USA 95, 12147-12152, 1998. |
|
(3) |
Coetzee T, Fujita N, Dupree J, Shi R, Blight A, Suzuki K,
Suzuki K, Popko B: Myelination in the absence of galactocerebroside
and sulfatide: normal structure with abnormal function and regional
instability. Cell 86, 209-219, 1996. |
|
(4) |
Bosio A, Binczek E, Stoffel W: Functional breakdown of the
lipid bilayer of the myelin membrane in central and peripheral
nervous system by disrupted galactocerebroside synthesis. Proc.
Natl. Acad. Sci. USA 93, 13280-13285, 1996. |
|
|
|
|
|