Abstract

Recently, glycosphingolipids have been attracting attention due to their role on biological systems as second messengers or modulators of signal transduction, affecting several events, which range from apoptosis to regulation of the cell cycle. In pathogenic fungi, glycolipids are expressed in two classes: neutral monohexosylceramides (glucosyl-or galactosylceramide) and acidic glycosylinositol phosphorylceramides (the latter class carries longer glycan chains). It is worth to mention that monohexosylceramides exhibit significant structural differences in their lipid moieties compared to their mammalian counterparts, whereas the glycosylinositol phosphorylceramides exhibit remarkable structural differences in their carbohydrate moieties in comparison to mammal glycosphingolipids counterpart. We observed that glycosylinositol phosphorylceramides are capable of promoting immune response in infected humans. In addition, inhibiting fungal glycosphingolipid biosynthetic pathways leads to an inhibition of colony formation, spore germination, cell cycle, dimorphism and hyphal growth. Other pathogens, such as trypanosomatids, also present unique glycolipids, which may have an important role for the parasite development and/or disease establishment. Regarding host-pathogen interaction, cell membrane rafts, which are enriched in sphingolipids and sterols, participate in parasite/fungal infection. In this review, it is discussed the different biological roles of (glyco) (sphingo)lipids of pathogenic/opportunistic fungi and trypanosomatids.

Highlights

  • This review is part of the celebration on the 75 years of Escola Paulista de Medicina/Universidade Federal de São Paulo

  • Several glycosylinositol phosphorylceramides (GIPCs) present long glycan moieties, which are built up, for example, on core “iii” (Scheme 1, Product 7), as it was described for P. brasiliensis, H. capsulatum, S. schenckii, A. fumigatus, A. nidulans, C. albicans and Cr. neoformans

  • The remarkable structural diversity of GIPCs observed in fungi is built up from three different cores: GlcNα12Ins, Manα1-2Ins and Manα1-6Ins

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Summary

Introduction

This review is part of the celebration on the 75 years of Escola Paulista de Medicina/Universidade Federal de São Paulo. Several GIPCs present long glycan moieties, which are built up, for example, on core “iii” (Scheme 1, Product 7), as it was described for P. brasiliensis, H. capsulatum, S. schenckii, A. fumigatus, A. nidulans, C. albicans and Cr. neoformans.

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