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Glyco-tuftsin derivatives modulate interleukin-1 and tumor necrosis factor production.

作者信息

Rocchi R, Biondi L, Filira F, Tzehoval E, Dagan S, Fridkin M

机构信息

Department of Organic Chemistry, University of Padova, Italy.

出版信息

Int J Pept Protein Res. 1991 Mar;37(3):161-6. doi: 10.1111/j.1399-3011.1991.tb00265.x.

DOI:10.1111/j.1399-3011.1991.tb00265.x
PMID:1869367
Abstract

Six Thr1 (O-glyco)-derivatives of the "phagocytosis stimulating peptide" tuftsin, H-Thr-Lys-Pro-Arg-OH and the N-glycosylated undecapeptide H-Thr-Lys-Pro-Arg-Glu-Gln-Gln-Tyr-Asn(beta-D-GlcNAc)-Ser-Thr-OH, which correspond to the "tuftsin-region" at the Fc-domain of immunoglobulin G (amino acid residues 289-299), were evaluated in comparison with tuftsin and rigin, H-Gly-Gln-Pro-Arg-OH, for their capacity to evoke the release of interleukin-1 and tumor necrosis factor from mouse peritoneal macrophages and from human monocytes. Several glycosylated tuftsin derivatives were found to modulate, in a rather dose-dependent manner, the release of the two cytokines from both cell types.

摘要

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