Bo. Choi et al., DELETION OF COMPLEX GANGLIOSIDES OF HUMAN GLIOMA-CELLS DURING MITOTICCELL-DIVISION, Journal of neuro-oncology, 34(3), 1997, pp. 211-219
Glycolipid compositions of the human glioma cell line T98G were studie
d during each phase of the cell cycle to see if those cell surface mol
ecules are concerned with cell proliferation. In vitro cultured nonsyn
chronized T98G cells are composed of ceramidemonohexoside (CMH), ceram
idedihexoside (CDH), ceramidetrihexoside (CTH) and neolactotetraosylce
ramide (nLc(4)Cer) as neutral glycolipids, and of sulfatide (CS), gang
liosides GM3, GM2, GD1a and several other gangliosides as acidic ones.
While total glycolipid content per cellular weight was shown to be in
creased during the M phase, deletion of complex gangliosides particula
rly b-series gangliosides was recognized (p < 0.05). The glycolipid pr
ofile in other phases was fairly consistent, and there was no glycolip
id molecule specific to a certain phase of the cell cycle. Relative en
hancement of simple gangliosides with a decrease of complex ones durin
g mitotic division may imply the functional involvement of complex gan
gliosides in cell-cell or cell-matrix attachment, which may have to be
abandoned during the process of detachment from the matrix or cellula
r cleavage.