Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/28273
Title: The C-terminus of murine S100A9 inhibits spreading and phagocytic activity of adherent peritoneal cells
Authors: Pagano, R. L.
Sampaio, S. C.
Juliano, L.
Juliano, M. A.
Giorgi, R.
Butantan Inst
Universidade Federal de São Paulo (UNIFESP)
Keywords: S100A9
adherent peritoneal cells
spreading
phagocytosis
zinc
Issue Date: 1-May-2005
Publisher: Birkhauser Verlag Ag
Citation: Inflammation Research. Basel: Birkhauser Verlag Ag, v. 54, n. 5, p. 204-210, 2005.
Abstract: Objective and design: in the present study, the effect of a synthetic peptide (H-92-G(102)) identical to the C-terminus of murine S100A9 (mS100A9p) was investigated on adherent peritoneal cell function.Materials and methods: for in vitro assays, peritoneal cells were obtained from the abdominal cavity of mice and incubated, with the different concentrations of mS100A9p, for 1 h, and then their spreading and phagocytosis activities were evaluated. for ex-vivo assays, cells obtained from animals treated for 1 h with the peptide were submitted to the mannose-receptor phagocytosis assay. Shorter homologue peptides to the C-terminus of mS100A9p were also evaluated on in vitro phagocytosis assays of Candida albicans particles.Results: mS100A9p reduced both the spreading index and phagocytic activity, in vitro and ex-vivo, independent of the receptor evaluated. the homologue peptide corresponding to the H-92-E-97 region of mS100A9p, the zinc-binding motif, was responsible for such an effect.Conclusion: These results suggest a modulator effect of the C-terminus of S100A9 protein on the function of adherent peritoneal cells.
URI: http://repositorio.unifesp.br/handle/11600/28273
ISSN: 1023-3830
Other Identifiers: http://dx.doi.org/10.1007/s00011-005-1344-y
Appears in Collections:Em verificação - Geral

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.