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
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.