Pityriarubins, novel highly selective inhibitors of respiratory burst from cultures of the yeast Malassezia furfur:: Comparison with the bisindolylmaleimide arcyriarubin A

被引:35
作者
Krämer, HJ
Kessler, D
Hipler, UC
Irlinger, B
Hort, W
Bödeker, RH
Steglich, W
Mayser, P
机构
[1] Univ Giessen, Ctr Androl & Dermatol, D-35385 Giessen, Germany
[2] Univ Jena, Dept Dermatol & Allergol, D-07740 Jena, Germany
[3] Univ Munich, Dept Chem, D-81377 Munich, Germany
[4] Justus Liebig Univ, Inst Med Informat, D-35585 Giessen, Germany
关键词
amino acids; granulocytes; Malassezia furfur; natural products; signalling;
D O I
10.1002/cbic.200500163
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pityriasis versicolor is the most common skin mycosis in humans worldwide. Yeasts of the genus Malassezia, particularly M. furfur a saprophyte occurring widely on human skin, are generally regarded as the causative agents. M. furfur is able to convert tryptophan into a variety of indole alkaloids, some of them showing biological properties that correlate well with certain clinical features of pityriasis versicolor. This suggests a possible role for these compounds in the pathophysiology of the disease. We here report that the novel pityriarubins A, B and C, isolated from cultures of the yeast, inhibit respiratory burst in human neutrophils, activated by various agents, in a highly selective, unexpected manner. The release of 5-lipoxygenose products after challenge of neutrophils with the calcium ionophore A23187 is also inhibited in a dose-dependent manner. These activities reflect the close structural relationship of pityriarubins to bisindolylmaleimides, which have recently gained great interest as protein kinase inhibitors.
引用
收藏
页码:2290 / 2297
页数:8
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