Macrophage depletion by liposome-encapsulated clodronate suppresses seizures but not hippocampal damage after acute viral encephalitis
Viral encephalitis is a major risk factor for the development of seizures and epilepsy, but the underlying mechanisms are only poorly understood. Mouse models such as viral encephalitis induced by intracerebral infection with Theiler's virus in C57BL/6 (B6) mice allow advancing our understandin...
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Published in: | Neurobiology of disease Vol. 110; pp. 192 - 205 |
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Abstract | Viral encephalitis is a major risk factor for the development of seizures and epilepsy, but the underlying mechanisms are only poorly understood. Mouse models such as viral encephalitis induced by intracerebral infection with Theiler's virus in C57BL/6 (B6) mice allow advancing our understanding of the immunological and virological aspects of infection-induced seizures and their treatment. Previous studies using the Theiler's virus model in B6 mice have indicated that brain-infiltrating inflammatory macrophages and the cytokines released by these cells are key to the development of acute seizures and hippocampal damage in this model. However, approaches used to prevent or reduce macrophage infiltration were not specific, so contribution of other mechanisms could not be excluded. In the present study, we used a more selective and widely used approach for macrophage depletion, i.e., systemic administration of clodronate liposomes, to study the contribution of macrophage infiltration to development of seizures and hippocampal damage. By this approach, almost complete depletion of monocytic cells was achieved in spleen and blood of Theiler's virus infected B6 mice, which was associated with a 70% decrease in the number of brain infiltrating macrophages as assessed by flow cytometry. Significantly less clodronate liposome-treated mice exhibited seizures than liposome controls (P<0.01), but the development of hippocampal damage was not prevented or reduced. Clodronate liposome treatment did not reduce the increased Iba1 and Mac3 labeling in the hippocampus of infected mice, indicating that activated microglia may contribute to hippocampal damage. The unexpected mismatch between occurrence of seizures and hippocampal damage is thought-provoking and suggests that the mechanisms involved in degeneration of specific populations of hippocampal neurons in encephalitis-induced epilepsy are more complex than previously thought.
•Theiler's virus can be used to induce seizures and epilepsy in C57BL/6 mice.•Infiltrating macrophages are thought to contribute to seizures and hippocampal damage in this model.•Here, clodronate liposomes were used to minimize macrophage infiltration into the brain.•Macrophage depletion suppressed seizures but not hippocampal damage.•Increased Mac3-immunolabeling indicated that microglia may contribute to hippocampal damage. |
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AbstractList | Viral encephalitis is a major risk factor for the development of seizures and epilepsy, but the underlying mechanisms are only poorly understood. Mouse models such as viral encephalitis induced by intracerebral infection with Theiler's virus in C57BL/6 (B6) mice allow advancing our understanding of the immunological and virological aspects of infection-induced seizures and their treatment. Previous studies using the Theiler's virus model in B6 mice have indicated that brain-infiltrating inflammatory macrophages and the cytokines released by these cells are key to the development of acute seizures and hippocampal damage in this model. However, approaches used to prevent or reduce macrophage infiltration were not specific, so contribution of other mechanisms could not be excluded. In the present study, we used a more selective and widely used approach for macrophage depletion, i.e., systemic administration of clodronate liposomes, to study the contribution of macrophage infiltration to development of seizures and hippocampal damage. By this approach, almost complete depletion of monocytic cells was achieved in spleen and blood of Theiler's virus infected B6 mice, which was associated with a 70% decrease in the number of brain infiltrating macrophages as assessed by flow cytometry. Significantly less clodronate liposome-treated mice exhibited seizures than liposome controls (P<0.01), but the development of hippocampal damage was not prevented or reduced. Clodronate liposome treatment did not reduce the increased Iba1 and Mac3 labeling in the hippocampus of infected mice, indicating that activated microglia may contribute to hippocampal damage. The unexpected mismatch between occurrence of seizures and hippocampal damage is thought-provoking and suggests that the mechanisms involved in degeneration of specific populations of hippocampal neurons in encephalitis-induced epilepsy are more complex than previously thought. Viral encephalitis is a major risk factor for the development of seizures and epilepsy, but the underlying mechanisms are only poorly understood. Mouse models such as viral encephalitis induced by intracerebral infection with Theiler's virus in C57BL/6 (B6) mice allow advancing our understanding of the immunological and virological aspects of infection-induced seizures and their treatment. Previous studies using the Theiler's virus model in B6 mice have indicated that brain-infiltrating inflammatory macrophages and the cytokines released by these cells are key to the development of acute seizures and hippocampal damage in this model. However, approaches used to prevent or reduce macrophage infiltration were not specific, so contribution of other mechanisms could not be excluded. In the present study, we used a more selective and widely used approach for macrophage depletion, i.e., systemic administration of clodronate liposomes, to study the contribution of macrophage infiltration to development of seizures and hippocampal damage. By this approach, almost complete depletion of monocytic cells was achieved in spleen and blood of Theiler's virus infected B6 mice, which was associated with a 70% decrease in the number of brain infiltrating macrophages as assessed by flow cytometry. Significantly less clodronate liposome-treated mice exhibited seizures than liposome controls (P<0.01), but the development of hippocampal damage was not prevented or reduced. Clodronate liposome treatment did not reduce the increased Iba1 and Mac3 labeling in the hippocampus of infected mice, indicating that activated microglia may contribute to hippocampal damage. The unexpected mismatch between occurrence of seizures and hippocampal damage is thought-provoking and suggests that the mechanisms involved in degeneration of specific populations of hippocampal neurons in encephalitis-induced epilepsy are more complex than previously thought. •Theiler's virus can be used to induce seizures and epilepsy in C57BL/6 mice.•Infiltrating macrophages are thought to contribute to seizures and hippocampal damage in this model.•Here, clodronate liposomes were used to minimize macrophage infiltration into the brain.•Macrophage depletion suppressed seizures but not hippocampal damage.•Increased Mac3-immunolabeling indicated that microglia may contribute to hippocampal damage. |
Author | Käufer, Christopher Anjum, Muneeb Löscher, Wolfgang Gerhauser, Ingo Ghita, Luca Kalinke, Ulrich Waltl, Inken Chhatbar, Chintan Bröer, Sonja |
Author_xml | – sequence: 1 givenname: Inken surname: Waltl fullname: Waltl, Inken organization: Department of Pharmacology, Toxicology, and Pharmacy, University of Veterinary Medicine Hannover, Germany – sequence: 2 givenname: Christopher surname: Käufer fullname: Käufer, Christopher organization: Department of Pharmacology, Toxicology, and Pharmacy, University of Veterinary Medicine Hannover, Germany – sequence: 3 givenname: Sonja surname: Bröer fullname: Bröer, Sonja organization: Department of Pharmacology, Toxicology, and Pharmacy, University of Veterinary Medicine Hannover, Germany – sequence: 4 givenname: Chintan surname: Chhatbar fullname: Chhatbar, Chintan organization: Institute for Experimental Infection Research, TWINCORE, Center for Experimental and Clinical Infection Research, a joint venture between the Helmholtz Center for Infection Research, Braunschweig, and the Hannover Medical School, Hannover, Germany – sequence: 5 givenname: Luca surname: Ghita fullname: Ghita, Luca organization: Institute for Experimental Infection Research, TWINCORE, Center for Experimental and Clinical Infection Research, a joint venture between the Helmholtz Center for Infection Research, Braunschweig, and the Hannover Medical School, Hannover, Germany – sequence: 6 givenname: Ingo surname: Gerhauser fullname: Gerhauser, Ingo organization: Department of Pathology, University of Veterinary Medicine Hannover, Germany – sequence: 7 givenname: Muneeb surname: Anjum fullname: Anjum, Muneeb organization: Department of Pharmacology, Toxicology, and Pharmacy, University of Veterinary Medicine Hannover, Germany – sequence: 8 givenname: Ulrich surname: Kalinke fullname: Kalinke, Ulrich organization: Institute for Experimental Infection Research, TWINCORE, Center for Experimental and Clinical Infection Research, a joint venture between the Helmholtz Center for Infection Research, Braunschweig, and the Hannover Medical School, Hannover, Germany – sequence: 9 givenname: Wolfgang surname: Löscher fullname: Löscher, Wolfgang email: wolfgang.loescher@tiho-hannover.de organization: Department of Pharmacology, Toxicology, and Pharmacy, University of Veterinary Medicine Hannover, Germany |
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Keywords | PBS IHC Epilepsy DAPI Neuroinflammation Iba1 TLE TMEV Gr-1 IL-6 Infection B6 ANOVA Mice DA Inflammatory monocytes FJC Hippocampus |
Language | English |
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SubjectTerms | Animals Cardiovirus Infections - complications Cardiovirus Infections - immunology Cardiovirus Infections - pathology Cell Movement - drug effects Clodronic Acid - administration & dosage Encephalitis, Viral - complications Encephalitis, Viral - immunology Encephalitis, Viral - pathology Epilepsy Hippocampus Hippocampus - pathology Infection Inflammatory monocytes Liposomes Macrophages - immunology Macrophages - metabolism Mice Mice, Inbred C57BL Neuroinflammation Seizures - immunology Theilovirus |
Title | Macrophage depletion by liposome-encapsulated clodronate suppresses seizures but not hippocampal damage after acute viral encephalitis |
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