SOLUBLE MANNAN AND BETA-GLUCAN INHIBIT THE UPTAKE OF MALASSEZIA-FURFUR BY HUMAN MONOCYTIC CELL-LINE, THP-1

Citation
T. Suzuki et al., SOLUBLE MANNAN AND BETA-GLUCAN INHIBIT THE UPTAKE OF MALASSEZIA-FURFUR BY HUMAN MONOCYTIC CELL-LINE, THP-1, FEMS immunology and medical microbiology, 21(3), 1998, pp. 223-230
Citations number
22
Categorie Soggetti
Immunology,Microbiology
ISSN journal
09288244
Volume
21
Issue
3
Year of publication
1998
Pages
223 - 230
Database
ISI
SICI code
0928-8244(1998)21:3<223:SMABIT>2.0.ZU;2-G
Abstract
The uptake of live and heat-killed Malassezia furfur HIC 3321, HIC 334 3 and Candida albicans ATCC 10231 by human monocytic cell line, THP-1, was examined. THP-1 was differentiated by PMA for 7 days before use. The uptake of these yeasts by THP-1 was increased in a concentration-d ependent manner of yeasts, and the uptake reached plateau level at the E/T (yeast/THP-1) ratio 5. In addition, a higher percentage of heat-k illed cells than live cells was taken in THP-1. Yeast mannan and beta- 1, 3-glucan, random coiled conformer, inhibited the uptake of live and heat-killed M. furfur by THP-1, though dextran T-250, that is alpha-g lucan, and schizophyllan (SPG), triple helix conformer of beta-glucan, did not. Interestingly, mannan inhibited the uptake of both types, li ve and heat-killed, of C. albicans, however, laminaran inhibited the u ptake of heat-killed C. albicans alone. Opsonization of these yeasts w ith normal human serum enhanced the uptake of yeasts, although opsoniz ation with heat-inactivated serum, the treatment at 56 degrees C for 3 0 min, did not enhance. These results suggested that live and heat-kil led M. furfur was recognized by THP-1 through mannose receptor, beta-g lucan receptor and complement receptor type 3 via the activation of al ternative pathway of complement. (C) 1998 Federation of European Micro biological Societies. Published by Elsevier Science B.V. All rights re served.