Merocytophagy is an integrin-stabilized macrophage response to microbes reliant on Syk signaling

Macrophages and dendritic cells acquire bacteria and cytosolic content from other cells without killing the donor cell through a trogocytosis-associated process termed merocytophagy. While characteristics of this behavior have been partially identified, the mechanism and potential contribution to the response to infection are unclear. Here, we reveal that a wide range of distinct species of bacteria stimulate enhanced merocytophagy in macrophages through pattern recognition receptor (PRR). Further, we found that cell-to-cell transfer in response to <i>Francisella tularensis</i> infection occurs in a predominantly MyD88-independent manner, relying on spleen tyrosine kinase (Syk) activity. Syk signaling during this response also results in increased surface expression of cell-to-cell adhesion proteins integrin α4, integrin β1, ICAM-1 and CD44 at the site of merocytophagy transfer, and depleting these surface molecules impairs merocytophagic cell-to-cell transfer. Altogether, our data demonstrate that merocytophagy is a host response to infection facilitated by tight cell-to-cell binding which molecularly resembles an immunological synapse between macrophages.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-04-17
DOI
https://doi.org/10.3389/fimmu.2025.1565250
Primary Topic
Phagocytosis and Immune Regulation
Type
article
Field-Weighted Citation Impact
0.00

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article

Merocytophagy is an integrin-stabilized macrophage response to microbes reliant on Syk signaling

Thomas H. Kawula, Shannon Whiles, Shaun Steele, Sedelia R Dominguez et al.
Frontiers in Immunology
Phagocytosis and Immune Regulation
article

Merocytophagy is an integrin-stabilized macrophage response to microbes reliant on Syk signaling

Thomas H. Kawula, Shannon Whiles, Shaun Steele, Sedelia R Dominguez, Kelly N. Deobald
article en

Abstract

Macrophages and dendritic cells acquire bacteria and cytosolic content from other cells without killing the donor cell through a trogocytosis-associated process termed merocytophagy. While characteristics of this behavior have been partially identified, the mechanism and potential contribution to the response to infection are unclear. Here, we reveal that a wide range of distinct species of bacteria stimulate enhanced merocytophagy in macrophages through pattern recognition receptor (PRR). Further, we found that cell-to-cell transfer in response to <i>Francisella tularensis</i> infection occurs in a predominantly MyD88-independent manner, relying on spleen tyrosine kinase (Syk) activity. Syk signaling during this response also results in increased surface expression of cell-to-cell adhesion proteins integrin α4, integrin β1, ICAM-1 and CD44 at the site of merocytophagy transfer, and depleting these surface molecules impairs merocytophagic cell-to-cell transfer. Altogether, our data demonstrate that merocytophagy is a host response to infection facilitated by tight cell-to-cell binding which molecularly resembles an immunological synapse between macrophages.

Frontiers in ImmunologyVol. 16
Washington State University (US)
National Institute of General Medical Sciences, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 91%
Phagocytosis and Immune Regulation
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Merocytophagy is an integrin-stabilized macrophage response to microbes reliant on Syk signaling — Thomas H. Kawula, Shannon Whiles, et al. · Frontiers in Immunology (2025) | TGRS Research Map | TGRS