Macrophages use sub-micron actin ridges in phagocytosis of encapsulated fungal pathogens

Ingestion and killing of pathogens by phagocytic cells is a key aspect of animal immunity. Cryptococcus neoformans is a major pathogen of AIDS patients that has a polysaccharide capsule that is critical for virulence. Phagocytic function is necessary for normal immunity to cryptococcal infection, and we sought to determine how Cryptococcus capsule prevents phagocytosis. In doing so, we discovered a new sub-micron actin structure, the ridge, that is present on macrophages, neutrophils and amoebae. Macrophages preferentially bind cryptococci via ridges and suppression of ridges is sufficient to prevent phagocytosis. Ridges are present on macrophages in vivo and are lost in interleukin 10 stimulated macrophages. The discovery and functional description of macrophage surface ridges fills a critical gap in our understanding of how phagocytes ingest encapsulated fungal pathogens, a crucial step in treating infection.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-02
DOI
https://doi.org/10.64898/2026.10.30.763038
Primary Topic
Fungal Infections and Studies
Type
preprint
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preprint

Macrophages use sub-micron actin ridges in phagocytosis of encapsulated fungal pathogens

Jason King, Heather L. Wilson, Simon Andrew Johnston, Lynne R. Prince et al.
bioRxiv (Cold Spring Harbor Laboratory)
Fungal Infections and Studies
preprint

Macrophages use sub-micron actin ridges in phagocytosis of encapsulated fungal pathogens

Jason King, Heather L. Wilson, Simon Andrew Johnston, Lynne R. Prince, Yin Xin Ho, Endré Kiss-Toth, James R. Bradford, Mahrukh Shameem, Taghreed Shumrani, Laura Campesino, Rhoda L Hawkins, Jaime Canedo
preprint en

Abstract

Ingestion and killing of pathogens by phagocytic cells is a key aspect of animal immunity. Cryptococcus neoformans is a major pathogen of AIDS patients that has a polysaccharide capsule that is critical for virulence. Phagocytic function is necessary for normal immunity to cryptococcal infection, and we sought to determine how Cryptococcus capsule prevents phagocytosis. In doing so, we discovered a new sub-micron actin structure, the ridge, that is present on macrophages, neutrophils and amoebae. Macrophages preferentially bind cryptococci via ridges and suppression of ridges is sufficient to prevent phagocytosis. Ridges are present on macrophages in vivo and are lost in interleukin 10 stimulated macrophages. The discovery and functional description of macrophage surface ridges fills a critical gap in our understanding of how phagocytes ingest encapsulated fungal pathogens, a crucial step in treating infection.

bioRxiv (Cold Spring Harbor Laboratory)
University of Sheffield (GB)
Good health and well-being
Fungal Infections and Studies
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