2006
DOI: 10.1128/iai.74.1.28-39.2006
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Role of Sphingolipids in Microbial Pathogenesis

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Cited by 196 publications
(173 citation statements)
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References 158 publications
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“…Although synthesis of sphingolipids is highly conserved between mammalian and fungal cells, some structural differences and roles in pathogenesis allow for these molecules to be considered a good target for new drugs [9]. Sphingolipids are abundant components of membranes in eukaryotic cells, playing a variety of roles in fungal cells specifically, such as heat stress response, signal transduction, endocytosis and apoptosis [9][10][11][12]. Particularly, some sphingolipids play an important role in fungal pathogenesis, such as inositolphosphoryl ceramide (IPC) and glucosylceramide (GlcCer).…”
mentioning
confidence: 99%
“…Although synthesis of sphingolipids is highly conserved between mammalian and fungal cells, some structural differences and roles in pathogenesis allow for these molecules to be considered a good target for new drugs [9]. Sphingolipids are abundant components of membranes in eukaryotic cells, playing a variety of roles in fungal cells specifically, such as heat stress response, signal transduction, endocytosis and apoptosis [9][10][11][12]. Particularly, some sphingolipids play an important role in fungal pathogenesis, such as inositolphosphoryl ceramide (IPC) and glucosylceramide (GlcCer).…”
mentioning
confidence: 99%
“…Indeed, even 'non-classic' infectious agents require lipid rafts, as demonstrated by the requirement for the prion proteins which partition into rafts during the conversion of PrP c to infectious PrP sc (Simons & Ehehalt, 2002). Bacteria often favour lipid rafts during host-cell interactions (Heung et al, 2006),. Raft association may provide a platform for colonisation, through signalling, cytoskeleton rearrangements and membrane ruffling (Manes & Martinez, 2004).…”
Section: Defining a New Assay For Lipid Raft Formationmentioning
confidence: 99%
“…Transcriptional studies on symbiotic cnidarians exposed to elevated temperature or high irradiance stress indicate that symbiont removal mechanisms such as host apoptosis, innate immunity and exocytosis are upregulated (DeSalvo et al, 2008;Richier et al, 2006;Starcevic et al, 2010). Modulation of sphingolipids could underlie these changes through activation of phagosomal maturation (Heung et al, 2006) and cell death (Maceyka et al, 2002). The cnidarian sphingosine rheostat has been implicated in symbiosis maintenance (Hemond et al, 2014;Rodriguez-Lanetty et al, 2006), immunity and the HSR (Detournay and Weis, 2011).…”
Section: Introductionmentioning
confidence: 99%
“…Although there have been extensive studies on dysbiosis in a variety of corals and sea anemone model systems (reviewed by Weis, 2008), our understanding of the cellular events preceding symbiont loss is limited. Given that lipids are co-directors of phagocytosis (Heung et al, 2006;Steinberg and Grinstein, 2008), the mode by which Symbiodinium are acquired by hosts, dysbiosis could have significant impacts on lipid signaling, targeting and trafficking events.…”
Section: Introductionmentioning
confidence: 99%