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Parasite immunology1987; 9(2); 195-204; doi: 10.1111/j.1365-3024.1987.tb00500.x

Inhibition of equine neutrophil chemotaxis and chemokinesis by a Taenia taeniaeformis proteinase inhibitor, taeniaestatin.

Abstract: Taeniaestatin, a recently isolated Taenia taeniaeformis proteinase inhibitor, was used to inhibit equine neutrophil migration. Taeniaestatin itself was not chemotactic when used as a chemotactic factor but taeniaestatin did inhibit neutrophil chemokinesis when tested in a Zigmond-Hirsch checkerboard assay. A dose-dependent inhibition of both chemokinesis and chemotaxis was observed when zymosan activated bovine sera (ZABS) was used as the chemotactic factor. This inhibition was greater than 95% when 5 mu of taeniaestatin was present on both the cell and chemotactic factor side of the chambers. Equine neutrophils gave dose- and time-dependent migration responses to purified bovine C5a with an ED50 of 1.04 X 10(-7)M. Taeniaestatin inhibited the C5a-mediated chemotactic and chemokinetic neutrophil responses (51% using 1 mu and greater than 95% with 5 mu of taeniaestatin). The inhibition of leucocyte motility by taeniaestatin was reversible and without cytotoxicity at the highest doses of taeniaestatin tested.
Publication Date: 1987-03-01 PubMed ID: 3574975DOI: 10.1111/j.1365-3024.1987.tb00500.xGoogle Scholar: Lookup
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  • Comparative Study
  • Journal Article
  • Research Support
  • U.S. Gov't
  • P.H.S.

Summary

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This research aims to understand how Taeniaestatin, a proteinase inhibitor from the parasite Taenia taeniaeformis, can inhibit the migration of equine (horse) neutrophils, a type of white blood cell.

Research Context

  • The research revolves around studying the effect of Taeniaestatin, a proteinase inhibitor present in the Taenia taeniaeformis parasite. The primary aim was to evaluate the impact of this protein on the migration of neutrophils, a type of white blood cell, in horses.
  • Proteinase inhibitors like Taeniaestatin are molecules that help decrease or block the action of proteases, which are enzymes that break down proteins. They are commonly found in different living organisms, including parasitic flatworms like the Taenia taeniaeformis.
  • Neutrophil migration refers to how these white blood cells move in response to different signals in their environment. This process is a key factor in the immune response as neutrophils seek out and destroy threats to the body.

Key Methods and Findings

  • Taeniaestatin was used in multiple experiments to analyze its effect on equine neutrophil migration. Experiments such as the Zigmond-Hirsch checkerboard assay were used and it was found that Taeniaestatin itself did not act as a stimulant for neutrophil movement (was not “chemotactic”). However, it did demonstrably hinder neutrophil movement.
  • It was noted that the presence of Taeniaestatin showed a dose-dependent inhibitory impact on both chemokinesis (random neutrophil movement) and chemotaxis (directed movement in response to a stimulus).
  • When taeniaestatin was introduced to both the neutrophils and a stimulus (zikosan activated bovine sera – ZABS), inhibition of chemokinesis and chemotaxis increased to over 95% efficiency when 5 microunits of taeniaestatin were used.
  • In response to another stimulus, bovine C5a, neutrophils exhibited dose- and time-dependent migration. But the presence of taeniaestatin still produced considerable inhibitory effects – 51% inhibition with 1 microunit, and over 95% inhibition with 5 microunits of taeniaestatin.
  • Lastly, the research established that the effect of Taeniaestatin on leukocyte (white blood cell) motility was reversible and it was not toxic to the cells, even at the highest concentrations used.

Implications

  • The results confirmed that Taeniaestatin has a significant inhibitory effect on equine neutrophil migration even without causing any cytotoxicity or cell damage.
  • This research could have wide implications, most notably in the field of immunology, for understanding how parasites, like Taenia taeniaeformis, may evade or disrupt host immune responses. It highlights a mechanism by which the parasites could potentially hinder the body’s immune response to infection.
  • The researched reversible inhibition suggests potential therapeutic applications where selective and temporary moderation of the immune response is desired, such as in autoimmune diseases or inflammatory disorders.

Cite This Article

APA
Leid RW, Grant RF, Suquet CM. (1987). Inhibition of equine neutrophil chemotaxis and chemokinesis by a Taenia taeniaeformis proteinase inhibitor, taeniaestatin. Parasite Immunol, 9(2), 195-204. https://doi.org/10.1111/j.1365-3024.1987.tb00500.x

Publication

ISSN: 0141-9838
NlmUniqueID: 7910948
Country: England
Language: English
Volume: 9
Issue: 2
Pages: 195-204

Researcher Affiliations

Leid, R W
    Grant, R F
      Suquet, C M

        MeSH Terms

        • Animals
        • Chemotactic Factors / pharmacology
        • Chemotaxis, Leukocyte / drug effects
        • Dose-Response Relationship, Drug
        • Helminth Proteins
        • Horses
        • Invertebrate Hormones / pharmacology
        • L-Lactate Dehydrogenase / metabolism
        • Neutrophils / drug effects
        • Neutrophils / metabolism
        • Taenia / physiology

        Grant Funding

        • 17913 / PHS HHS

        Citations

        This article has been cited 6 times.
        1. Garcia HH, Gonzalez AE, Gilman RH. Taenia solium Cysticercosis and Its Impact in Neurological Disease.. Clin Microbiol Rev 2020 Jun 17;33(3).
          doi: 10.1128/CMR.00085-19pubmed: 32461308google scholar: lookup
        2. Evans H, Killoran KE, Mitre BK, Morris CP, Kim SY, Mitre E. Ten Weeks of Infection with a Tissue-Invasive Helminth Protects against Local Immune Complex-Mediated Inflammation, but Not Cutaneous Type I Hypersensitivity, in Previously Sensitized Mice.. J Immunol 2015 Oct 1;195(7):2973-84.
          doi: 10.4049/jimmunol.1500081pubmed: 26324775google scholar: lookup
        3. Rees-Roberts D, Mullen LM, Gounaris K, Selkirk ME. Inactivation of the complement anaphylatoxin C5a by secreted products of parasitic nematodes.. Int J Parasitol 2010 Apr;40(5):527-32.
          doi: 10.1016/j.ijpara.2009.10.006pubmed: 19874826google scholar: lookup
        4. Robinson P, Atmar RL, Lewis DE, White AC Jr. Granuloma cytokines in murine cysticercosis.. Infect Immun 1997 Jul;65(7):2925-31.
        5. Matsubara S, Yamamoto T, Tsuruta T, Takagi K, Kambara T. Complement C4-derived monocyte-directed chemotaxis-inhibitory factor. A molecular mechanism to cause polymorphonuclear leukocyte-predominant infiltration in rheumatoid arthritis synovial cavities.. Am J Pathol 1991 May;138(5):1279-91.
          pubmed: 2024711
        6. Blackburn CC, Selkirk ME. Inactivation of platelet-activating factor by a putative acetylhydrolase from the gastrointestinal nematode parasite Nippostrongylus brasiliensis.. Immunology 1992 Jan;75(1):41-6.
          pubmed: 1537601