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1.
Carbohydr Res ; 328(4): 459-66, 2000 Oct 06.
Artigo em Inglês | MEDLINE | ID: mdl-11093701

RESUMO

The major glycosphingolipid in pig vascular endothelium is the ceramide pentasaccharide Gal alpha(1 --> 3)Gal beta(1 --> 4)GlcNAc beta(1 --> 3)Gal beta(1 --> 4)Glc beta(1 --> 0)Cer (1), which binds specifically to human anti-Gal antibody and is involved in the hyperacute rejection response in xenotransplantation from pig to man. The synthesis of 1 and its methyl glycoside 2 is described.


Assuntos
Antígenos Heterófilos/biossíntese , Glicoesfingolipídeos/síntese química , Rejeição de Enxerto/imunologia , Oligossacarídeos/síntese química , Transplante Heterólogo/imunologia , Animais , Anticorpos Heterófilos/imunologia , Antígenos Heterófilos/efeitos adversos , Antígenos Heterófilos/química , Configuração de Carboidratos , Sequência de Carboidratos , Endotélio Vascular/química , Galactose/imunologia , Glicoesfingolipídeos/imunologia , Humanos , Dados de Sequência Molecular , Suínos , Transplante Heterólogo/efeitos adversos
3.
Chemistry ; 6(1): 111-22, 2000 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-10747394

RESUMO

Sialyl Lewis X (sLeX)/selectin-mediated leukocyte rolling along endothelial cells has recently gained wide interest. In this paper the influence of the spacer length of laterally clustered neoglycolipids 1a-d on cell rolling in a dynamic test system is investigated. The required di-O-hexadecyl glycerols with none, and with three, six, or nine ethylene glycol units as spacer groups (compounds 4a-d) could be readily obtained. The synthesis of 1-O-thexyldimethylsilyl-protected sLeX 24 was based on sialylation of 2,3,4-O-unprotected galactose derivative 11 with sialyl phosphite 8 as donor; this afforded the desired disaccharide 12, which was transformed into trichloroacetimidate 14 as disaccharide donor. Reaction of 3-O-unprotected glucosamine derivative 18 with fucosyl donor 20 afforded disaccharide 21, which was transformed into the 4-O-unprotected derivative 23. Reaction of 14 with 23 furnished the desired tetrasaccharide 24 in good yield. Transformation of 24 into the trichloroacetimidate 26 as donor, followed by the reaction with 4a-d as acceptor gave, after deprotection, the target molecules 1a-d. For comparison, 4d was also connected with a sialyl residue (-->31) and with an N-acetylglucosamine residue (-->34). Compounds 1c and 1d with a hexaethylene glycol and a nonaethylene glycol spacer, respectively, were much more efficient in mediating selectin-dependent cell rolling in the dynamic test system than compounds 1a and 1b, which had no spacer (1a), or only a triethylene glycol spacer (1b).


Assuntos
Glicolipídeos/química , Glicolipídeos/metabolismo , Antígenos CD15/química , Oligossacarídeos/química , Selectinas/metabolismo , Animais , Células CHO/metabolismo , Sequência de Carboidratos , Adesão Celular , Cricetinae , Epitopos/química , Glicolipídeos/síntese química , Antígenos CD15/imunologia , Dados de Sequência Molecular , Oligossacarídeos/imunologia , Antígeno Sialil Lewis X , Relação Estrutura-Atividade
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