Species restrictions demonstrated by the stimulation of equine cells with recombinant human interleukin-1.
Abstract: Equine thymocytes, which respond to equine monocyte supernatants, do not respond to stimulation with recombinant human interleukin-1 alpha and beta, and equine synovial fibroblasts show a limited response in the form of prostaglandin E2 production without any evidence of neutral metalloproteinase production. Human interleukin-1 beta was about three to ten times as active on equine synovial cells as human interleukin-1 alpha in terms of prostaglandin E2 production. This preliminary evidence would suggest that there are qualitative and quantitative differences in the way recombinant human interleukin-1 stimulates human cells and the way in which it stimulates equine cells.
Publication Date: 1992-01-31 PubMed ID: 1546442DOI: 10.1016/0165-2427(92)90106-zGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research investigated how the stimulation of horse cells with synthetic human interleukin-1 resulted to distinct outcomes, indicating species-specific reactions. The study highlighted how equine synovial fibroblasts and equine thymocytes responded differently or not at all to these synthetic human proteins.
Explanation of Equine Thymocyte Response
- The study recorded that equine thymocytes, a type of lymphocyte developed within the thymus of horses, didn’t respond to stimulation from synthetic human interleukin-1 alpha and beta. This reaction was in stark contrast to their response to equine monocyte supernatants.
- This suggests that these proteins operates in a species-specific manner with minimal cross-reactivity between species. Hence, understanding this aspect is crucial in the development of targeted immunotherapies or diagnostics for equine diseases.
Response of Equine Synovial Fibroblasts
- Equine synovial fibroblasts, the cells responsible for the maintenance of joint health in horses, showed a limited reaction to the synthetic human interleukin-1 proteins. Their response was observed in the production of prostaglandin E2, a hormone-like compound that plays a role in inflammation and pain. However, these cells did not produce neutral metalloproteinase.
- This contrastingly limited response reflects a qualitative difference in the way equine cells respond to human interleukin-1 proteins, further reaffirming the species-specific nature of these immunological interactions.
Differential Activity of Human Interleukin-1 Alpha and Beta
- It was also noted that human interleukin-1 beta was three to ten times more effective than human interleukin-1 alpha at inducing prostaglandin E2 production in equine synovial cells.
- This shows that not only the species, but also the type of interleukin-1 protein, played a role in determining the extent and nature of the cellular response.
Implications and Conclusions
- This research indicates that the interactions between human interleukin-1 and equine cells demonstrate both qualitative and quantitative differences when compared to the interactions between these proteins and human cells.
- Such insights into species-specific cell responses can help advance medical and veterinary science, potentially leading to the development of better techniques for boosting immune response and treating various diseases and conditions in animals.
Cite This Article
APA
May SA, Hooke RE, Lees P.
(1992).
Species restrictions demonstrated by the stimulation of equine cells with recombinant human interleukin-1.
Vet Immunol Immunopathol, 30(4), 373-384.
https://doi.org/10.1016/0165-2427(92)90106-z Publication
Researcher Affiliations
- Department of Veterinary Basic Sciences, Royal Veterinary College, Hatfield, Herfordshire, UK.
MeSH Terms
- Animals
- Dinoprostone / metabolism
- Fibroblasts / immunology
- Horses / immunology
- Humans
- Interleukin-1 / immunology
- Lymphocyte Activation / immunology
- Recombinant Proteins / immunology
- Species Specificity
- Synovial Fluid / immunology
- T-Lymphocytes / immunology
- Thymus Gland / immunology
Citations
This article has been cited 1 times.- Tung JT, Fenton JI, Arnold C, Alexander L, Yuzbasiyan-Gurkan V, Venta PJ, Peters TL, Orth MW, Richardson DW, Caron JP. Recombinant equine interleukin-1beta induces putative mediators of articular cartilage degradation in equine chondrocytes. Can J Vet Res 2002 Jan;66(1):19-25.
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