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Systemic inflammation modulates Fc receptor expression on microglia during chronic neurodegeneration

Systemic inflammation modulates Fc receptor expression on microglia during chronic neurodegeneration
Systemic inflammation modulates Fc receptor expression on microglia during chronic neurodegeneration
Chronic neurodegeneration is a major worldwide health problem, and it has been suggested that systemic inflammation can accelerate the onset and progression of clinical symptoms. A possible explanation is that systemic inflammation “switches” the phenotype of microglia from a relatively benign to a highly aggressive and tissue damaging phenotype. The current study investigated the molecular mechanism underlying this microglia phenotype “switching.” We show in mice with chronic neurodegeneration (ME7 prion model) that there is increased expression of receptors that have a key role in macrophage activation and associated signaling pathways, including TREM-2, Siglec-F, CD200R, and IgG Fc receptors (FcgRs). Systemic inflammation induced by LPS further increased protein levels of the activating FcgRIII and FcgRIV, but not of other microglial receptors, including the inhibitory FcgRII. In addition to these changes in receptor expression, IgG levels in the brain parenchyma were increased during chronic neurodegeneration, and these IgG levels further increased after systemic inflammation. g Chain–deficient mice show modified proinflammatory cytokine expression in the brain after systemic inflammation. We conclude that systemic inflammation during chronic neurodegeneration increases the expression levels of activating FcgR on microglia and thereby lowers the signaling threshold for Ab-mediated cell activation. At the same time, IgG influx into the brain could provide a cross linking ligand resulting in excessive microglia activation that is detrimental to neurons already under threat by misfolded protein.
0022-1767
7215-7224
Lunnon, Katie
c28c4d27-24b2-4f2a-8c25-f32b11fc29f7
Teeling, Jessica L.
fcde1c8e-e5f8-4747-9f3a-6bdb5cd87d0a
Tutt, Alison L.
46ce577b-aea1-412d-84ea-fc4dab794469
Cragg, Mark S.
ec97f80e-f3c8-49b7-a960-20dff648b78c
Glennie, Martin J.
9f6f0eff-4560-48c2-80cd-0ec116110ded
Perry, V. Hugh
8f29d36a-8e1f-4082-8700-09483bbaeae4
Lunnon, Katie
c28c4d27-24b2-4f2a-8c25-f32b11fc29f7
Teeling, Jessica L.
fcde1c8e-e5f8-4747-9f3a-6bdb5cd87d0a
Tutt, Alison L.
46ce577b-aea1-412d-84ea-fc4dab794469
Cragg, Mark S.
ec97f80e-f3c8-49b7-a960-20dff648b78c
Glennie, Martin J.
9f6f0eff-4560-48c2-80cd-0ec116110ded
Perry, V. Hugh
8f29d36a-8e1f-4082-8700-09483bbaeae4

Lunnon, Katie, Teeling, Jessica L., Tutt, Alison L., Cragg, Mark S., Glennie, Martin J. and Perry, V. Hugh (2011) Systemic inflammation modulates Fc receptor expression on microglia during chronic neurodegeneration. Journal of Immunology, 186 (12), 7215-7224. (doi:10.4049/jimmunol.0903833).

Record type: Article

Abstract

Chronic neurodegeneration is a major worldwide health problem, and it has been suggested that systemic inflammation can accelerate the onset and progression of clinical symptoms. A possible explanation is that systemic inflammation “switches” the phenotype of microglia from a relatively benign to a highly aggressive and tissue damaging phenotype. The current study investigated the molecular mechanism underlying this microglia phenotype “switching.” We show in mice with chronic neurodegeneration (ME7 prion model) that there is increased expression of receptors that have a key role in macrophage activation and associated signaling pathways, including TREM-2, Siglec-F, CD200R, and IgG Fc receptors (FcgRs). Systemic inflammation induced by LPS further increased protein levels of the activating FcgRIII and FcgRIV, but not of other microglial receptors, including the inhibitory FcgRII. In addition to these changes in receptor expression, IgG levels in the brain parenchyma were increased during chronic neurodegeneration, and these IgG levels further increased after systemic inflammation. g Chain–deficient mice show modified proinflammatory cytokine expression in the brain after systemic inflammation. We conclude that systemic inflammation during chronic neurodegeneration increases the expression levels of activating FcgR on microglia and thereby lowers the signaling threshold for Ab-mediated cell activation. At the same time, IgG influx into the brain could provide a cross linking ligand resulting in excessive microglia activation that is detrimental to neurons already under threat by misfolded protein.

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More information

Published date: 15 June 2011
Organisations: Cancer Sciences, Clinical Neurosciences, Biological Sciences

Identifiers

Local EPrints ID: 185569
URI: http://eprints.soton.ac.uk/id/eprint/185569
ISSN: 0022-1767
PURE UUID: a5879c0a-a86d-4eb6-947f-959ea1656289
ORCID for Jessica L. Teeling: ORCID iD orcid.org/0000-0003-4004-7391
ORCID for Mark S. Cragg: ORCID iD orcid.org/0000-0003-2077-089X

Catalogue record

Date deposited: 10 May 2011 15:14
Last modified: 15 Mar 2024 03:21

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Contributors

Author: Katie Lunnon
Author: Alison L. Tutt
Author: Mark S. Cragg ORCID iD
Author: V. Hugh Perry

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