A CERAMIDE ANALOG (PDMP) INHIBITS GLYCOLIPID SYNTHESIS IN FISH EMBRYOS

被引:41
作者
FENDERSON, BA
OSTRANDER, GK
HAUSKEN, Z
RADIN, NS
HAKOMORI, S
机构
[1] BIOMEMBRANE INST,SEATTLE,WA 98119
[2] OKLAHOMA STATE UNIV,DEPT ZOOL,STILLWATER,OK 74078
[3] UNIV MICHIGAN,MENTAL HLTH RES INST,ANN ARBOR,MI 48109
关键词
D O I
10.1016/0014-4827(92)90392-L
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glycolipids were depleted from medaka embryos using 1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP), an inhibitor of glucosylceramide synthetase. Embryos cultured in the presence of 20 μM PDMP exhibited a dramatic decline in glycolipid synthesis and cell surface expression. Metabolic labeling of glucosylceramide declined by 87% on Days 3-6 of development and 72% on Days 7-10 (hatching occurred on Day 10). In parallel, PDMP-treated embryos exhibited a striking loss of several tissue-specific glycolipid antigens, including 9-O-acetyl GD3 from brain and retina, GT3/ GQ1C from brain, neural tube, and retina, and sulfated glycolipid from skin and gut. Despite these changes in glycolipid expression, PDMP-treated embryos were fully viable with no evidence of developmental abnormality. PDMP appears to provide a useful tool for identifying glycolipid antigens in embryos and investigating their role in development. © 1992.
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页码:362 / 366
页数:5
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