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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1994-12-12
pubmed:abstractText
The biosynthesis of neolacto glycosphingolipids is thought to proceed via reactions catalysed by the two enzymes beta 1-3-N-acetylglucosaminyltransferase (beta 1,3GlcNAcT) and beta 1-4 galactosyltransferase (beta 1,4GalT). In general, only the products of the latter enzyme have been isolated from tissues and structurally characterized. Among the GlcNAc beta 1-3-R glycosphingolipids, only lactotrioasylceramide (Lc3Cer, the initial product in the biosynthesis of neolacto glycosphingolipids) has been isolated and structurally characterized. Longer-chain glycosphingolipids with a terminal GlcNAc-beta 1-3-R structure are considered to be intermediates in the synthesis of complex neolacto glycosphingolipids. We have detected a series of GlcNAc beta 1-3-R glycosphingolipids in extracts obtained from human leukocytes isolated from patients with leukaemia using a monoclonal antibody (TE5) which specifically recognizes these compounds. The structures of three of these compounds purified from chronic myelocytic leukaemia (CML) cells have been determined using a combination of enzymatic, immunostaining and chemical methods. The compounds were found to have the following structures: GlcNAc beta 1-3Gal beta 1-4Glc beta 1-1Cer (Lc3Cer) GlcNAc beta 1-3Gal beta 1-4GlcNAc beta 1-3Gal beta 1-4Glc beta 1-1Cer (nLc5Cer) GlcNAc beta 1-3Gal beta 1-4GlcNAc beta 1-3Gal beta 1-4GlcNAc beta 1-3Gal beta 1-4Glc beta 1-1Cer (nLc7Cer) A longer-chain compound, apparently nLc9Cer, was also detected. TLC immunostaining analysis of glycosphingolipids isolated from cells obtained from patients with various leukaemias demonstrated that GlcNAc beta 1-3-R glycosphingolipids have a distribution that depends on the stage of differentiation and lineage of the cell population.(ABSTRACT TRUNCATED AT 250 WORDS)
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0959-6658
pubmed:author
pubmed:issnType
Print
pubmed:volume
4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
251-7
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:7949652-Carbohydrate Sequence, pubmed-meshheading:7949652-Cell Differentiation, pubmed-meshheading:7949652-Galactosyltransferases, pubmed-meshheading:7949652-Glycosphingolipids, pubmed-meshheading:7949652-Humans, pubmed-meshheading:7949652-Leukemia, pubmed-meshheading:7949652-Leukemia, Lymphocytic, Chronic, B-Cell, pubmed-meshheading:7949652-Leukemia, Myelogenous, Chronic, BCR-ABL Positive, pubmed-meshheading:7949652-Leukemia, Myeloid, Acute, pubmed-meshheading:7949652-Leukemia, Myelomonocytic, Acute, pubmed-meshheading:7949652-Methylation, pubmed-meshheading:7949652-Molecular Sequence Data, pubmed-meshheading:7949652-N-Acetylglucosaminyltransferases, pubmed-meshheading:7949652-Precursor Cell Lymphoblastic Leukemia-Lymphoma, pubmed-meshheading:7949652-Tumor Cells, Cultured
pubmed:year
1994
pubmed:articleTitle
Structural characterization of intermediates in the biosynthetic pathway of neolacto glycosphingolipids: differential expression in human leukaemia cells.
pubmed:affiliation
Department of Chemistry and Biochemistry, San Francisco State University, CA 94132.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.