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Calreticulin and Galectin-3 Opsonise Bacteria for Phagocytosis by Microglia

Accepted version
Peer-reviewed

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Type

Article

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Authors

Cockram, Tom OJ 
Puigdellívol, Mar 
Brown, Guy C 

Abstract

Opsonins are soluble, extracellular proteins, released by activated immune cells, and when bound to a target cell, can induce phagocytes to phagocytose the target cell. There are three known classes of opsonin: antibodies, complement factors and secreted pattern recognition receptors, but these have limited access to the brain. We identify here two novel opsonins of bacteria, calreticulin, and galectin-3 (both lectins that can bind lipopolysaccharide), which were released by microglia (brain-resident macrophages) when activated by bacterial lipopolysaccharide. Calreticulin and galectin-3 both bound to Escherichia coli, and when bound increased phagocytosis of these bacteria by microglia. Furthermore, lipopolysaccharide-induced microglial phagocytosis of E. coli bacteria was partially inhibited by: sugars, an anti-calreticulin antibody, a blocker of the calreticulin phagocytic receptor LRP1, a blocker of the galectin-3 phagocytic receptor MerTK, or simply removing factors released from the microglia, indicating this phagocytosis is dependent on extracellular calreticulin and galectin-3. Thus, calreticulin and galectin-3 are opsonins, released by activated microglia to promote clearance of bacteria. This innate immune response of microglia may help clear bacterial infections of the brain.

Description

Keywords

LRP1, MerTK, bacteria, calreticulin, galectin-3, microglia, opsonin, Animals, Brain, Calreticulin, Escherichia coli, Escherichia coli Infections, Galectin 3, Immunity, Innate, Mice, Microglia, Opsonin Proteins, Phagocytosis, Rats

Journal Title

Frontiers in Immunology

Conference Name

Journal ISSN

1664-3224
1664-3224

Volume Title

10

Publisher

Frontiers Media SA

Rights

All rights reserved
Sponsorship
Medical Research Council (MR/L010593/1)
Biotechnology and Biological Sciences Research Council (1645643)
This work was funded by the Biotechnology & Biological Sciences Research Council UK and the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement No. 115976 (PHAGO consortium).