» Articles » PMID: 19917081

The C5a Anaphylatoxin Receptor CD88 is Expressed in Presynaptic Terminals of Hippocampal Mossy Fibres

Overview
Publisher Biomed Central
Date 2009 Nov 18
PMID 19917081
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Background: In the periphery, C5a acts through the G-protein coupled receptor CD88 to enhance/maintain inflammatory responses. In the brain, CD88 can be expressed on astrocytes, microglia and neurons. Previous studies have shown that the hippocampal CA3 region displays CD88-immunolabelling, and CD88 mRNA is present within dentate gyrus granule cells. As granule cells send dense axonal projections (mossy fibres) to CA3 pyramidal neurons, CD88 expression could be expressed on mossy fibres. However, the cellular location of CD88 within the hippocampal CA3 region is unknown.

Methods: The expression of CD88 within the hippocampal CA3 region was characterized using dual-immunolabelling of hippocampal sections prepared from Wistar rats. Immunolabelling for CD88, using a monoclonal antibody, was combined with immunolabelling for markers of astrocytes (GFAP), microglia (IBA1), presynaptic proteins (synaptophysin and synapsin-1) and preterminal axons (neurofilament). In addition, electron microscopy was performed on peroxidase-visualized CD88-immunolabelling to determine its cellular localisation within the CA3 region.

Results: Dense CD88-immunolabelling was observed within the stratum lucidum of the CA3, consistent with the presence of CD88 on mossy fibres. Labelling for CD88 rarely co-localized with astrocytes or microglia, but was highly co-localized with presynaptic proteins. Electron microscopy revealed CD88-immunolabelling was localized to large presynaptic terminals within the stratum lucidum.

Conclusion: These results demonstrate that CD88 is expressed on presynaptic terminals of mossy fibres within the CA3 region of the hippocampus. Although the role of CD88 on mossy fibres remains to be established, their involvement in synaptic/cellular plasticity, and in cognitive disorders such as Alzheimer's disease deserves investigation.

Citing Articles

Epigenetic mechanisms of alveolar macrophage activation in chemical-induced acute lung injury.

Ahmad S, Nasser W, Ahmad A Front Immunol. 2024; 15:1488913.

PMID: 39582870 PMC: 11581858. DOI: 10.3389/fimmu.2024.1488913.


Complement C5a Implication in Axonal Growth After Injury.

Cotten A, Jeanneau C, Decherchi P, About I Cells. 2024; 13(20.

PMID: 39451247 PMC: 11506376. DOI: 10.3390/cells13201729.


Glial Cells as Key Regulators in Neuroinflammatory Mechanisms Associated with Multiple Sclerosis.

Theophanous S, Sargiannidou I, Kleopa K Int J Mol Sci. 2024; 25(17).

PMID: 39273535 PMC: 11395575. DOI: 10.3390/ijms25179588.


Complement C5a Receptor Signaling Alters Stress Responsiveness and Modulates Microglia Following Chronic Stress Exposure.

Chen H, Spiers J, Lerskiatiphanich T, Parker S, Lavidis N, Fung J Biol Psychiatry Glob Open Sci. 2024; 4(3):100306.

PMID: 38628385 PMC: 11019103. DOI: 10.1016/j.bpsgos.2024.100306.


C5aR1 signaling promotes region- and age-dependent synaptic pruning in models of Alzheimer's disease.

Gomez-Arboledas A, Fonseca M, Kramar E, Chu S, Schartz N, Selvan P Alzheimers Dement. 2024; 20(3):2173-2190.

PMID: 38278523 PMC: 10984438. DOI: 10.1002/alz.13682.


References
1.
Ilschner S, Nolte C, Kettenmann H . Complement factor C5a and epidermal growth factor trigger the activation of outward potassium currents in cultured murine microglia. Neuroscience. 1996; 73(4):1109-20. DOI: 10.1016/0306-4522(96)00107-8. View

2.
Farkas I, Takahashi M, Fukuda A, Yamamoto N, Akatsu H, Baranyi L . Complement C5a receptor-mediated signaling may be involved in neurodegeneration in Alzheimer's disease. J Immunol. 2003; 170(11):5764-71. DOI: 10.4049/jimmunol.170.11.5764. View

3.
Mukherjee P, Pasinetti G . The role of complement anaphylatoxin C5a in neurodegeneration: implications in Alzheimer's disease. J Neuroimmunol. 2000; 105(2):124-30. DOI: 10.1016/s0165-5728(99)00261-1. View

4.
Sudhof T, Jahn R . Proteins of synaptic vesicles involved in exocytosis and membrane recycling. Neuron. 1991; 6(5):665-77. DOI: 10.1016/0896-6273(91)90165-v. View

5.
Klos A, Tenner A, Johswich K, Ager R, Reis E, Kohl J . The role of the anaphylatoxins in health and disease. Mol Immunol. 2009; 46(14):2753-66. PMC: 2725201. DOI: 10.1016/j.molimm.2009.04.027. View