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Role of Cellular Metabolism during Candida-Host Interactions
Kings Coll London, Fac Dent, Ctr Host Microbiome Interact, Oral & Craniofacial Sci, London, England..
Kings Coll London, Fac Dent, Ctr Host Microbiome Interact, Oral & Craniofacial Sci, London, England..
Kings Coll London, Fac Dent, Ctr Host Microbiome Interact, Oral & Craniofacial Sci, London, England..
Kings Coll London, Fac Dent, Ctr Host Microbiome Interact, Oral & Craniofacial Sci, London, England..
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2022 (engelsk)Inngår i: Pathogens, E-ISSN 2076-0817, Vol. 11, nr 2, artikkel-id 184Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Microscopic fungi are widely present in the environment and, more importantly, are also an essential part of the human healthy mycobiota. However, many species can become pathogenic under certain circumstances, with Candida spp. being the most clinically relevant fungi. In recent years, the importance of metabolism and nutrient availability for fungi-host interactions have been highlighted. Upon activation, immune and other host cells reshape their metabolism to fulfil the energy-demanding process of generating an immune response. This includes macrophage upregulation of glucose uptake and processing via aerobic glycolysis. On the other side, Candida modulates its metabolic pathways to adapt to the usually hostile environment in the host, such as the lumen of phagolysosomes. Further understanding on metabolic interactions between host and fungal cells would potentially lead to novel/enhanced antifungal therapies to fight these infections. Therefore, this review paper focuses on how cellular metabolism, of both host cells and Candida, and the nutritional environment impact on the interplay between host and fungal cells.

sted, utgiver, år, opplag, sider
MDPI AG , 2022. Vol. 11, nr 2, artikkel-id 184
Emneord [en]
immunometabolism, metabolism, macrophages, epithelial cells, glycolysis, glucose, moonlighting proteins, Candida albicans
HSV kategori
Identifikatorer
URN: urn:nbn:se:kth:diva-310586DOI: 10.3390/pathogens11020184ISI: 000771749300001PubMedID: 35215128Scopus ID: 2-s2.0-85123979623OAI: oai:DiVA.org:kth-310586DiVA, id: diva2:1649884
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QC 20220405

Tilgjengelig fra: 2022-04-05 Laget: 2022-04-05 Sist oppdatert: 2022-06-25bibliografisk kontrollert

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