AI Article Synopsis

  • The most common cause of fungal infections in humans is candidiasis, which is especially deadly in hospital settings and often leads to bloodstream infections with high mortality rates.
  • Research indicates that Nedd4 is crucial for proper signaling through immune receptors Dectin-1 and Dectin-2/3, affecting the immune response against fungal infections.
  • Mice lacking Nedd4 show increased susceptibility to systemic infections and impaired immune responses, indicating that Nedd4 is necessary for effective antifungal immunity by regulating specific signaling pathways in immune cells.

Article Abstract

is the most common cause of fungal infections in humans, and disseminated candidiasis has become one of the leading causes of hospital-acquired bloodstream infections with a high mortality rate. However, little is known about the host-pathogen interactions and the mechanisms of antifungal immunity. Here, we report that Nedd4 (neuronal precursor cell-expressed developmentally downregulated 4) is essential for signaling through Dectin-1 and Dectin-2/3. We showed that mice that lack Nedd4 globally or only in the myeloid compartment are highly susceptible to systemic infection, which correlates with heightened organ fungal burden, defective inflammatory response, impaired leukocyte recruitment to the kidneys, and defective reactive oxygen species expression by granulocytes. At the molecular level, macrophages displayed impaired activation of TGF-β-activating kinase-1 and NF-κB, but normal activation of spleen tyrosine kinase and protein kinase C-δ on yeast and hyphal infections. These data suggest that Nedd4 regulates signaling events downstream of protein kinase C-δ but upstream of or at TGF-β-activating kinase-1.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8324540PMC
http://dx.doi.org/10.4049/jimmunol.2100083DOI Listing

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