BIOSYNTHESIS OF GLYCOSPHINGOLIPIDS BY HUMAN MYELOID-LEUKEMIA CELLS

被引:19
作者
BUEHLER, J
QWAN, E
DEGREGORIO, MW
MACHER, BA
机构
[1] UNIV CALIF SAN FRANCISCO, CANC RES INST, SAN FRANCISCO, CA 94143 USA
[2] UNIV CALIF SAN FRANCISCO, DEPT PHARMACEUT CHEM, SAN FRANCISCO, CA 94143 USA
[3] PACIFIC PRESBYTERIAN MED CTR, CHILDRENS CANC RES INST, SAN FRANCISCO, CA 94115 USA
关键词
D O I
10.1021/bi00345a034
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 have performed comparative studies of the neutral glycosphingolipids synthesized by three human myeloid leukemia cell lines, K562, KG1, and HL-60, which were metabolically labeled with [14C]galactose, to evaluate changes in neutral glycosphingolipid synthesis with myeloid cell differentiation. Individual neutral glycosphingolipids containing one to four sugars were purified by a combination of the following methods: diethylaminoethyl-Sephadex column chromatography, acetylation-Florisil column chromatography, and high-performance liquid chromatography using an Iatrobead column. Compounds with one sugar were analyzed by thin-layer chromatography on borate plates. This analysis showed that HL-60 cells synthesize only glucosylceramide, whereas K562 ad KG1 cells synthesize predominately glucosylceramide, but also a small amount of galactosylceramide. Compounds with two to four sugars were characterized by treatment with exo- and endoglycosidases. The results showed that K562 and KG1 cells are similar to cells from patients with acute leukemia in expressing two series (globo and neolacto) of natural glycosphingolipids, whereas the HL-60 cells are similar to mature human myeloid cells in expressing only one series (neolacto). Therefore, human myeloid leukemia cells blocked at different stages of differentiation vary in their ability to synthesize neutral glycosphingolipids.
引用
收藏
页码:6978 / 6984
页数:7
相关论文
共 36 条
[1]   CONTINUOUS GROWTH AND DIFFERENTIATION OF HUMAN MYELOID LEUKEMIC-CELLS IN SUSPENSION CULTURE [J].
COLLINS, SJ ;
GALLO, RC ;
GALLAGHER, RE .
NATURE, 1977, 270 (5635) :347-349
[2]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[3]   IDENTIFICATION BY A MONOCLONAL-ANTIBODY OF A GLYCOLIPID HIGHLY EXPRESSED BY CELLS FROM THE HUMAN MYELOID LINEAGE [J].
GIRARDET, C ;
LADISCH, S ;
HEUMANN, D ;
MACH, JP ;
CARREL, S .
INTERNATIONAL JOURNAL OF CANCER, 1983, 32 (02) :177-183
[4]   MARKER OF PERIPHERAL-BLOOD GRANULOCYTES AND MONOCYTES OF MAN RECOGNIZED BY 2 MONOCLONAL-ANTIBODIES VEP8 AND VEP9 INVOLVES THE TRISACCHARIDE 3-FUCOSYL-N-ACETYLLACTOSAMINE [J].
GOOI, HC ;
THORPE, SJ ;
HOUNSELL, EF ;
RUMPOLD, H ;
KRAFT, D ;
FORSTER, O ;
FEIZI, T .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1983, 13 (04) :306-312
[5]  
HAKOMORI SI, 1971, J BIOL CHEM, V246, P2271
[6]  
HUANG LC, 1983, BLOOD, V61, P1020
[7]   ACCUMULATION OF GLYCOLIPIDS CONTAINING N-ACETYLGLUCOSAMINE IN ERYTHROCYTE STROMA OF PATIENTS WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-2 (HEMPAS) [J].
JOSEPH, KC ;
GOCKERMAN, JP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1975, 65 (01) :146-152
[8]  
KANNAGI R, 1983, BLOOD, V62, P1230
[9]  
KEAN EL, 1966, J LIPID RES, V7, P449
[10]  
KLOCK JC, 1981, J LIPID RES, V22, P1079