IMPAIRED GLYCOSYLATION OF GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHOR SYNTHESIS IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA LEUKOCYTES

被引:32
作者
HIDAKA, M
NAGAKURA, S
HORIKAWA, K
KAWAGUCHI, T
IWAMOTO, N
KAGIMOTO, T
TAKATSUKI, K
NAKAKUMA, H
机构
[1] KUMAMOTO UNIV,SCH MED,DEPT INTERNAL MED 2,BIOMEMBRANE RES LAB,KUMAMOTO 860,JAPAN
[2] KUMAMOTO UNIV,COLL MED SCI,KUMAMOTO 862,JAPAN
关键词
D O I
10.1006/bbrc.1993.1256
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
Metabolic labeling with [3H]sugars in vivo or [3H]sugar nucleotides in vitro of glycosylphosphatidylinositol (GPI)-anchor precursors in peripheral blood granulocytes and cultured T lymphocytes of paroxysmal nocturnal hemoglobinuria (PNH) patients showed a synthetic defect in the GPI-anchor. Among the GPI-anchor precursors, phosphatidylinositol (PI) was normally synthesized, while the synthesis of glucosaminylphosphatidylinositol (GlcN-PI) and subsequent mannosylation of GlcN-PI were inhibited in affected cells. The defect in the GPI-anchor synthesis in PNH is thus attributed to interrupted glycosylation at plural sites in the synthesis of the common carbohydrate structure of the anchor. © 1993 Academic Press.
引用
收藏
页码:571 / 579
页数:9
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