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Veterinary immunology and immunopathology2013; 157(3-4); 155-163; doi: 10.1016/j.vetimm.2013.12.001

Isolation and characterization of equine nasal mucosal CD172a + cells.

Abstract: The nasal mucosa surface is continuously confronted with a broad variety of environmental antigens, ranging from harmless agents to potentially harmful pathogens. This area is under rigorous control of professional antigen presenting cells (APCs), such as dendritic cells (DCs) and macrophages. Mucosal APCs play a crucial role in inducing primary immune responses and the establishment of an immunological memory. In the present study, a detailed characterization of CD172a(+) cells, containing the APCs residing in the equine nasal mucosa was performed for the first time. CD172a(+) cells were isolated from collagenase-treated equine nasal mucosa fragments by MACS. Expression of surface markers was determined by flow cytometry and functional analysis was done by measuring the uptake of FITC conjugated ovalbumin (FITC-OVA). Cell surface phenotype of the isolated cells was as follows: 90% CD172a(+), 30% CD1c(+), 46% CD83(+), 42% CD206(+) and 28% MHC II(+). This clearly differs from the phenotype of blood-derived monocytes: 96% CD172a(+), 4% CD1c(+), 11% CD83(+), 9% CD206(+), 72% MHC II(+) and blood monocyte derived DCs: 99% CD172a(+), 13% CD1c(+), 30% CD83(+), 51% CD206(+) and 93% MHC II(+). The CD172a(+) nasal mucosal cells were functionally able to endocytose FITC-OVA but to a lesser degree than monocyte-derived DCs. Together, these results demonstrate that the isolated CD172a(+) nasal mucosal cells resemble immature DCs in the nasal area.
Publication Date: 2013-12-06 PubMed ID: 24370377DOI: 10.1016/j.vetimm.2013.12.001Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research investigates and offers a detailed exploration of CD172a(+) cells, a type of antigen-presenting cells (APCs), which are found in the nasal mucosa of horses. The nature and functionality of these cells are further compared against blood-derived monocytes and dendritic cells (DCs).

Research Methodology

  • The researchers intensely focused on the antigen-presenting cells (APCs) such as macrophages and dendritic cells, found in the nasal mucosa. They identified these cells to play a vital role in generating primary immune responses and the establishment of immunological memory.
  • They isolated CD172a(+) cells from the collagenase-treated equine nasal mucosa fragments using the magnetic-activated cell sorting (MACS) process.
  • They used flow cytometry to ascertain the expression of surface markers. Flow cytometry is a common technique that allows researchers to measure physical and chemical characteristics of a population of cells or particles.
  • The functionality of the cells was then determined by measuring the uptake of FITC–OVA (Ovalbumin conjugated with a Fluorescein isothiocyanate). This measurement provides an understanding of the cell’s capacity to absorb and process antigens.

Research Findings

  • The study found that the cell surface phenotype of the isolated cells were 90% CD172a(+), 30% CD1c(+), 46% CD83(+), 42% CD206(+) and 28% MHC II(+).
  • This phenotype variation was different from that of blood-derived monocytes, which was 96% CD172a(+), 4% CD1c(+), 11% CD83(+), 9% CD206(+), 72% MHC II(+).
  • The phenotype of blood monocyte derived DCs was 99% CD172a(+), 13% CD1c(+), 30% CD83(+), 51% CD206(+) and 93% MHC II(+).
  • The CD172a(+) nasal mucosal cells were functionally capable of endocytosing FITC-OVA, but to a lesser degree than monocyte-derived DCs. Endocytosis is a process where the cells absorb materials from outside their cell membrane.

Conclusion

  • The findings suggest that the characterized CD172a(+) nasal mucosal cells can effectively function as antigen presenting cells (APCs), thus they hold pivotal roles in immune responses.
  • Importantly, these findings denote that the CD172a(+) nasal mucosal cells closely resemble immature dendritic cells in the nasal area. This knowledge improves our understanding of mucosal immunity, particularly in equines.

Cite This Article

APA
Baghi HB, Laval K, Favoreel H, Nauwynck HJ. (2013). Isolation and characterization of equine nasal mucosal CD172a + cells. Vet Immunol Immunopathol, 157(3-4), 155-163. https://doi.org/10.1016/j.vetimm.2013.12.001

Publication

ISSN: 1873-2534
NlmUniqueID: 8002006
Country: Netherlands
Language: English
Volume: 157
Issue: 3-4
Pages: 155-163
PII: S0165-2427(13)00316-4

Researcher Affiliations

Baghi, Hossein Bannazadeh
  • Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium.
Laval, Kathlyn
  • Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium.
Favoreel, Herman
  • Laboratory of Immunology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium.
Nauwynck, Hans J
  • Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium. Electronic address: hans.nauwynck@ugent.be.

MeSH Terms

  • Animals
  • Antigen-Presenting Cells / immunology
  • Antigens, Differentiation / analysis
  • Cell Separation
  • Horses
  • Nasal Mucosa / immunology

Citations

This article has been cited 6 times.
  1. Van Crombrugge E, Vanbeylen E, Van Cleemput J, Van den Broeck W, Laval K, Nauwynck H. Bacterial Toxins from Staphylococcus aureus and Bordetella bronchiseptica Predispose the Horse's Respiratory Tract to Equine Herpesvirus Type 1 Infection. Viruses 2022 Jan 14;14(1).
    doi: 10.3390/v14010149pubmed: 35062352google scholar: lookup
  2. Laval K, Poelaert KCK, Van Cleemput J, Zhao J, Vandekerckhove AP, Gryspeerdt AC, Garré B, van der Meulen K, Baghi HB, Dubale HN, Zarak I, Van Crombrugge E, Nauwynck HJ. The Pathogenesis and Immune Evasive Mechanisms of Equine Herpesvirus Type 1. Front Microbiol 2021;12:662686.
    doi: 10.3389/fmicb.2021.662686pubmed: 33746936google scholar: lookup
  3. Kolyvushko O, Kelch MA, Osterrieder N, Azab W. Equine Alphaherpesviruses Require Activation of the Small GTPases Rac1 and Cdc42 for Intracellular Transport. Microorganisms 2020 Jul 7;8(7).
    doi: 10.3390/microorganisms8071013pubmed: 32645930google scholar: lookup
  4. Lee Y, Kiupel M, Soboll Hussey G. Characterization of respiratory dendritic cells from equine lung tissues. BMC Vet Res 2017 Nov 6;13(1):313.
    doi: 10.1186/s12917-017-1240-zpubmed: 29110660google scholar: lookup
  5. Zhao J, Poelaert KCK, Van Cleemput J, Nauwynck HJ. CCL2 and CCL5 driven attraction of CD172a(+) monocytic cells during an equine herpesvirus type 1 (EHV-1) infection in equine nasal mucosa and the impact of two migration inhibitors, rosiglitazone (RSG) and quinacrine (QC). Vet Res 2017 Feb 27;48(1):14.
    doi: 10.1186/s13567-017-0419-4pubmed: 28241864google scholar: lookup
  6. Negussie H, Li Y, Tessema TS, Nauwynck HJ. Replication characteristics of equine herpesvirus 1 and equine herpesvirus 3: comparative analysis using ex vivo tissue cultures. Vet Res 2016 Jan 15;47:19.
    doi: 10.1186/s13567-016-0305-5pubmed: 26768993google scholar: lookup