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Cell surface sialylation and fucosylation are regulated by the cell recognition molecule L1 via PLCgamma and cooperate to modulate embryonic stem cell survival and proliferation.

Authors :
Li YL
Wu GZ
Zeng L
Dawe GS
Sun L
Loers G
Tilling T
Cui SS
Schachner M
Xiao ZC
Source :
FEBS letters [FEBS Lett] 2009 Feb 18; Vol. 583 (4), pp. 703-10. Date of Electronic Publication: 2009 Jan 21.
Publication Year :
2009

Abstract

Cell surface glycosylation patterns are markers of cell type and status. However, the mechanisms regulating surface glycosylation patterns remain unknown. Using a panel of carbohydrate markers, we have shown that cell surface sialylation and fucosylation are upregulated in L1-transfected embryonic stem cells (L1-ESCs). Consistently, the mRNA levels of sialyltransferase ST6Gal1 and ST3Gal4, and fucosyltransferase FUT9 were significantly increased in L1-transfected ESCs. Activation of L1 signaling promoted cell survival and inhibited cell proliferation. ShRNAs knocking down FUT9, ST6Gal1 and ST3Gal4 blocked these effects. A phospholipase Cgamma (PLCgamma) inhibitor and shRNA reduced ST6Gal1, ST3Gal4 and FUT9 mRNA levels in the L1-ESCs. Thus, embryonic stem cell surface sialylation and fucosylation are regulated via PLCgamma by L1, with which they cooperate to modulate cell survival and proliferation.

Details

Language :
English
ISSN :
1873-3468
Volume :
583
Issue :
4
Database :
MEDLINE
Journal :
FEBS letters
Publication Type :
Academic Journal
Accession number :
19166842
Full Text :
https://doi.org/10.1016/j.febslet.2009.01.013