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Chondroitin sulfate B exerts its inhibitory effect on secondary lymphoid tissue chemokine (SLC) by binding to the C-terminus of SLC

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BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
卷 1571, 期 3, 页码 219-224

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ELSEVIER SCIENCE BV
DOI: 10.1016/S0304-4165(02)00232-5

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chemokine; secondary lymphoid tissue chemokine (SLC); CC chemokine receptor (CCR) 7; glycosaminoglycan; chondroitin sulfate B; chondroitin sulfate E

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We previously reported that certain glycosaminoglycans (GAGs) bind secondary lymphoid tissue chemokine (SLC, CCL21) and that the SLC-binding GAGs, including chondroitin sulfate B (CS B), negatively modulate the function of SLC, although the mechanism remains unknown [J. Biol. Chem. 276 (2001) 5228]. To gain insight into the mechanism of inhibition, we used a C-terminally truncated SLC (SLC-T) that lacked clusters of basic amino acid residues that have been implicated in GAG binding. While SLC-T failed to bind any GAGs, it induced prominent intracellular Ca2+ mobilization in CC chemokine receptor (CCR) 7-expressing cells, as did wild-type SLC. However, the SLC-T-induced Ca2+ influx was not inhibited by CS B, unlike the SLC-induced Ca2+ influx. These results demonstrate the requirement of the C-terminus of SLC for the inhibition of chemokine responses by CS B; that is, CS B exerts its inhibitory effect by binding to the C-terminus of SLC, thus defining the mode of action of CS B on certain chemokines. (C) 2002 Elsevier Science B.V. All rights reserved.

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