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Published on: June 23, 2013
Polarization of Macrophages in Epidural Inflammation Induced by Canine Intervertebral Disc Herniation
Núria Vizcaíno Revés1, Helga Maria Mogel2, Michael Stoffel2
1Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
Insights
Canine intervertebral disc herniation involves a mixed population of macrophages (M1 and M2), indicating the disease
Area of Science:
- Veterinary Pathology
- Immunology
- Canine Health
Background:
- Intervertebral disc (IVD) herniation in dogs typically presents with macrophages (Mϕ).
- Macrophages exist as distinct phenotypes: M1 (pro-inflammatory) and M2 (anti-inflammatory/healing).
- Understanding Mϕ phenotype in canine IVD disease is crucial for disease characterization.
Purpose of the Study:
- To characterize the macrophage phenotype in naturally occurring canine IVD herniation.
- To investigate the M1/M2 balance in affected intervertebral discs.
Main Methods:
- Immunohistochemistry was used on canine IVD samples from dogs with and without herniation.
- Markers CD14 (Mϕ), MHCII (M1), and CD206 (M2) were utilized.
- Cryostat sections were analyzed for macrophage populations.
Main Results:
- No macrophages were detected in healthy control canine IVD samples.
- Canine IVD herniation samples showed a mixed population of M1 and M2 macrophages.
- Some macrophages exhibited markers for both M1 and M2 phenotypes simultaneously.
Conclusions:
- Canine IVD herniation involves a dynamic and mixed macrophage phenotype.
- This mixed phenotype suggests a chronic component to IVD disease, even with acute clinical signs.
- Macrophage plasticity is evident in the pathogenesis of canine IVD disease.
Abstract:
Introduction: Canine interverterbral disc (IVD), although physiologically acellular, displays an inflammatory cell population consisting almost exclusively of macrophages (Mϕ) when acutely herniated. Mϕ encompass a heterogenous cell population, roughly divided into classically (M1) or alternatively activated (M2)Mϕ. Polarization into M1 Mϕ leads to strong antimicrobial activity and pro-inflammatory response. In contrast, M2Mϕ exibit anti-inflammatory function and regulate wound healing. The purpose of this study was to characterize the phenotype of the Mϕ population present in naturally occurring IVD herniation. Materials and Methods: IVD material of dogs with IVD disease was collected during standard decompressive surgery. A negative control consisting of IVD material of dogs without IVD degeneration and a positive control consisting of canine liver and lymph node samples were also included. All samples were embedded in OCT and shock frozen. Eight micrometer cryostat sections were prepared, air dried and immunostained without prefixation or permeabilization. CD14 was used as marker Mϕ, MHCII for M1Mϕ and CD206 for M2Mϕ. Results: Fifteen samples of dogs with IVD herniation, 10 negative, and 5 positive control samples were obtained. No positive cell was found in the negative control group. The positive control group displayed several MHCII and CD206 positive cells, all of them being simultaneously positive to CD14. All herniated samples displayed a mixed population of M1Mϕ and M2Mϕ, and some sparse Mϕ displaying markers for both M1 and M2Mϕ simultaneously. Conclusion: The mixed phenotype encountered shows the plasticity and dynamism of Mϕ and evidences the chronic component of IVD disease despite its acute clinical presentation.
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Herniated Intervertebral Disc l: Introduction
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