Crosstalk Between Autophagy and Hypoxia-Inducible Factor-l[alpha] in Antifungal Immunity

• Published in: Cells (Basel, Switzerland) Vol. 9; no. 10; p. 1
• Main Authors: Quaschling, Tim, Friedrich, Dirk, Deepe, George S., Jr, Rupp, Jan
• Format: Journal Article
• Language: English
• Published: MDPI AG 01.10.2020
• Subjects: Antifungal agents; Autophagy (Cytology); Dosage and administration; Immune response; Observations; Physiological aspects; Transcription factors; Germany
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells9102150

Modern medicine is challenged by several potentially severe fungal pathogens such as Aspergillus fumigatus, Candida albicans, or Histoplasma capsulatum. Though not all fungal pathogens have evolved as primary pathogens, opportunistic pathogens can still cause fatal infections in immuno-compromised patients. After infection with these fungi, the ingestion and clearance by innate immune cells is an important part of the host immune response. Innate immune cells utilize two different autophagic pathways, the canonical pathway and the non-canonical pathway, also called microtubule-associated protein 1A/1B-light chain 3 (LC3) -associated pathway (LAP), to clear fungal pathogens from the intracellular environment. The outcome of autophagy-related host immune responses depends on the pathogen and cell type. Therefore, the understanding of underlying molecular mechanisms of autophagy is crucial for the development and improvement of antifungal therapies. One of those molecular mechanisms is the interaction of the transcription-factor hypoxia-inducible factor 1[alpha] (HIF-1[alpha]) with the autophagic immune response. During this review, we will focus on a comprehensive overview of the role of autophagy and HIF-1[alpha] on the outcome of fungal infections.