The role of proliferation in the regulation of interferon gamma (IFNγ) expression in foals.
Abstract: Interferon-gamma (IFNγ) plays an important role against viral and intracellular bacterial infections and its production is deficient in foals. Cellular proliferation provides an opportunity for de novo gene expression, though little is known about its role in regulating IFNγ expression in foals. While stimulation of foal peripheral blood mononuclear cells (PBMCs) with concanavalin A (ConA) increased the frequency of IFNγ(+) cells, the overall percentage of IFNγ(+) cells remained below that of adults. By contrast, the proliferative response of foal PBMC was significantly greater than that of the adults. In foals, IFNγ production was predominantly associated with those T cells that underwent proliferation, whereas in adults non-dividing cells also produced IFNγ. While treatment with hydroxyurea inhibited cellular division, it failed to completely block IFNγ production. This residual IFNγ production likely represented memory cells as the proportion of these proliferation-independent IFNγ(+) cells increased with foal age. However, memory cells may not account for all of the IFNγ production as ConA stimulation likely provided additional signals that can control IFNγ expression.
Copyright © 2011 Elsevier Ltd. All rights reserved.
Publication Date: 2011-11-04 PubMed ID: 22079897DOI: 10.1016/j.dci.2011.09.009Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research investigates how cell proliferation, or growth, impacts the production of Interferon-gamma (IFNγ), a protein crucial for combating viral and bacterial infections, in young horses known as foals. The results reveal that most IFNγ in foals is produced by their proliferating T cells, unlike in adults where also non-dividing cells produce this protein.
Study on Interferon-gamma in Foals
- This study examined the key role that cellular proliferation, or growth, plays in the production of a protein called Interferon-gamma (IFNγ) in foals. IFNγ is vital for defending against viral and bacterial infections. However, in foals, its production is deficient.
- The researchers stimulated foal peripheral blood mononuclear cells (PBMCs)—white blood cells that are a critical part of the immune system—with Concanavalin A (ConA). This increased the number of cells that produced IFNγ but not to the same level as adults.
- Interestingly, they found that the act of cellular growth in foal PBMCs was significantly higher than in adults.
The Role of Proliferation in IFNγ Production
- The research revealed that in foals, IFNγ is predominantly produced by T cells that have undergone growth. However, in adult animals, the protein is also produced by non-dividing cells.
- The team also used hydroxyurea, a substance known to suppress cell division, in their study. They found that while it did impede cellular division, it did not entirely prevent production of IFNγ in foals.
- This suggested that the residual IFNγ production might be linked to memory cells—immune cells that remember how to fight off infections they’ve encountered before. The proportion of these independent IFNγ producing cells seemed to increase with foal age. However, memory cells may not be solely responsible for all of the IFNγ production, as the ConA stimulation may have also provided additional signals controlling IFNγ expression.
Implications of the Research
- This study provides new insights into the deficit of the crucial infection-fighting protein, IFNγ, in foals, offering potential pathways to improve their immunity. It highlights the importance of cellular proliferation in the regulation of the protein, presenting a new avenue for possible studies on enhancing IFNγ production through manipulation of cellular growth.
Cite This Article
APA
Sun L, Adams AA, Betancourt A, Stewart JC, Liu C, Horohov DW.
(2011).
The role of proliferation in the regulation of interferon gamma (IFNγ) expression in foals.
Dev Comp Immunol, 36(3), 534-539.
https://doi.org/10.1016/j.dci.2011.09.009 Publication
Researcher Affiliations
- Maxwell H. Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, KY 40546-0099, USA.
MeSH Terms
- Aging / immunology
- Animals
- Cell Proliferation
- Concanavalin A / metabolism
- Gene Expression
- Horses / immunology
- Horses / physiology
- Immunologic Memory
- Interferon-gamma / genetics
- Leukocytes, Mononuclear / cytology
- T-Lymphocytes / cytology
Citations
This article has been cited 1 times.- Tallmadge RL, Miller SC, Parry SA, Felippe MJB. Antigen-specific immunoglobulin variable region sequencing measures humoral immune response to vaccination in the equine neonate.. PLoS One 2017;12(5):e0177831.
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