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Veterinary research2004; 35(1); 39-51; doi: 10.1051/vetres:2003041

Immunophenotypic characterization and depletion of pulmonary intravascular macrophages of horses.

Abstract: Pulmonary intravascular macrophages (PIMs) are present in horses and are believed to increase their sensitivity to endotoxin-induced cardio-pulmonary shock. However, owing to a lack of a marker for PIMs and the inability to isolate them, their precise contributions in the horse remain unknown. We designed this study to identify an immuno-phenotypic marker for PIMs and to develop a protocol for their transient depletion with gadolinium chloride (GC). GC is a lanthanide that has been used to deplete liver and lung macrophages. The horses (N = 15) were divided into control (n = 5) and GC-treated (n = 10) groups and the lung samples were examined by routine and immunocytochemical light and electron microscopy. GC-treated horses were euthanized at 48 h (n = 6) and 72 h (n = 4) post-treatment. The PIMs reacted with MAC-387 but not with ED-1 and CD-68 anti-macrophage antibodies. GC reduced the number of PIMs in horses at 48 and 72 h compared with the control (p < 0.05). There were increased intravascular TUNEL-positive cells in GC-treated horses and electron microscopy showed apoptotic PIMs in these horses. These data show that MAC-387 is a reliable marker for PIMs and GC is a safe tool to reduce the number of PIMs.
Publication Date: 2004-04-22 PubMed ID: 15099502DOI: 10.1051/vetres:2003041Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research focuses on identifying a marker for pulmonary intravascular macrophages (PIMs) in horses, cells believed to make them more susceptible to severe reactions from endotoxins. They found that MAC-387 serves as a reliable marker and that a lanthanide group substance, gadolinium chloride (GC), can safely reduce the number of these macrophages.

Background and Objective

The researchers wanted to explore PIMs in horses, as their role was largely unknown due to past difficulties in isolating and identifying these cells. Their objective was to identify a specific marker for PIMs and establish a procedure for decreasing PIM numbers using GC, which has been demonstrated to deplete macrophages in liver and lung tissues.

Methodology

  • A total of 15 horses were divided into two sets: a control group of 5 horses and a GC-treated group of 10 horses.
  • Samples of lung tissue were taken from all participating animals and examined with light and electron microscopy both in ordinary and immunocytochemical settings.
  • The horses treated with GC were euthanized at either 48 hours (6 horses) or 72 hours (4 horses) following treatment.

Findings

  • The PIMs in the horses reacted to the MAC-387 antibody but not to the ED-1 or CD-68 anti-macrophage antibodies, designating MAC-387 as a legitimate marker for these cells.
  • The researchers observed a statistically significant decrease in the number of PIMs at both 48 and 72 hours post-treatment with GC, compared to the control group.
  • There was an observed increase in TUNEL-positive cells within the blood vessels of GC-treated horses, which is indicative of cellular apoptosis or programmed cell death.
  • Apoptotic PIMs were observed in GC-treated horses via electron microscopy.

Conclusion

The findings suggest that MAC-387 can be used as a reliable marker for identifying PIMs in horses. Additionally, gadolinium chloride or GC is a safe and effective tool to reduce the number of these PIMs. These findings provide a foundation for further research into the role of PIMs and their contribution to the sensitivity of horses to endotoxins and may also potentially lead to the development of treatments reducing the severity of endotoxin-induced shock in horses.

Cite This Article

APA
Parbhakar OP, Duke T, Townsend HG, Singh B. (2004). Immunophenotypic characterization and depletion of pulmonary intravascular macrophages of horses. Vet Res, 35(1), 39-51. https://doi.org/10.1051/vetres:2003041

Publication

ISSN: 0928-4249
NlmUniqueID: 9309551
Country: England
Language: English
Volume: 35
Issue: 1
Pages: 39-51

Researcher Affiliations

Parbhakar, Om P
  • Department of Veterinary Biomedical Sciences, Western College of Veterinary Medicine, 52 Campus Drive, University of Saskatchewan, Saskatoon, SK S7N 5B4, Canada.
Duke, Tanya
    Townsend, Hugh G G
      Singh, Baljit

        MeSH Terms

        • Animals
        • Anti-Inflammatory Agents / pharmacology
        • Apoptosis / drug effects
        • Biomarkers
        • Contrast Media / pharmacology
        • Gadolinium / pharmacology
        • Horses / immunology
        • Immunohistochemistry / veterinary
        • Immunophenotyping / veterinary
        • In Situ Nick-End Labeling / veterinary
        • Lung / cytology
        • Lung / pathology
        • Lung / ultrastructure
        • Macrophages, Alveolar / immunology
        • Macrophages, Alveolar / ultrastructure
        • Microscopy, Electron / methods
        • Microscopy, Electron / veterinary
        • Microscopy, Immunoelectron / veterinary
        • Random Allocation

        Citations

        This article has been cited 7 times.
        1. Townsend M, Fowler B, Aulakh GK, Singh B. Expression of pentraxin 3 in equine lungs and neutrophils.. Can J Vet Res 2023 Jan;87(1):9-16.
          pubmed: 36606044
        2. Bocking T, Singh B. Light and electron-microscopic localization of CD9 and surfactant protein A and D in normal lungs of the horse.. Can J Vet Res 2021 Jul;85(3):170-176.
          pubmed: 34248260
        3. Bocking T, Johnson L, Singh A, Desai A, Aulakh GK, Singh B. Research article expression of surfactant protein-A and D, and CD9 in lungs of 1 and 30 day old foals.. BMC Vet Res 2021 Jul 5;17(1):236.
          doi: 10.1186/s12917-021-02943-5pubmed: 34225699google scholar: lookup
        4. Le NPK, Gerdts V, Singh B. Integrin alpha-v/beta3 expression in equine lungs and jejunum.. Can J Vet Res 2020 Oct;84(4):245-251.
          pubmed: 33012972
        5. Schneberger D, Caldwell S, Kanthan R, Singh B. Expression of Toll-like receptor 9 in mouse and human lungs.. J Anat 2013 May;222(5):495-503.
          doi: 10.1111/joa.12039pubmed: 23521717google scholar: lookup
        6. Schneberger D, Lewis D, Caldwell S, Singh B. Expression of toll-like receptor 9 in lungs of pigs, dogs and cattle.. Int J Exp Pathol 2011 Feb;92(1):1-7.
        7. Gill SS, Suri SS, Janardhan KS, Caldwell S, Duke T, Singh B. Role of pulmonary intravascular macrophages in endotoxin-induced lung inflammation and mortality in a rat model.. Respir Res 2008 Oct 24;9(1):69.
          doi: 10.1186/1465-9921-9-69pubmed: 18950499google scholar: lookup