Molecular cloning, sequencing, and expression of equine interleukin-6

C. E. Swiderski, G. Sobol, D. P. Lunn, D. W. Horohov

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Equine interleukin-6 (IL-6) cDNA was amplified from mitogen-stimulated equine peripheral blood mononuclear cells (PBMC) using consensus sequence primers. The 727 bp amplified cDNA contains the entire coding region for equine IL-6 and includes 118 bases in the 3′ non-translated region. The coding sequence translates to a protein of 208 amino acids with a predicted 28 amino acid leader sequence. The mature protein of 180 amino acids has a predicted molecular mass of 20 471 Da without post-translational modifications. The amino acid sequence of equine IL-6 displays between 46 and 84% similarity to other mammalian IL-6 sequences. Expression of equine IL-6 in Chinese hamster ovary (CHO) cells yielded a supernatant that supported the proliferation of B9 cells in a dose-dependent manner. Treatment of B9 cells with an anti-IL-6 receptor antibody ablated the response to the recombinant equine IL-6.

Original languageEnglish
Pages (from-to)213-220
Number of pages8
JournalVeterinary Immunology and Immunopathology
Volume77
Issue number3-4
DOIs
StatePublished - Dec 29 2000

Bibliographical note

Funding Information:
This work was supported by an NIH Idea award, the Grayson Jockey Club Research Foundation, and the Louisiana State University’s Equine Health Studies Program.

Funding

This work was supported by an NIH Idea award, the Grayson Jockey Club Research Foundation, and the Louisiana State University’s Equine Health Studies Program.

FundersFunder number
National Institutes of Health (NIH)
Grayson Jockey Club Research Foundation Inc
Louisiana State University

    Keywords

    • Equine interleukin-6 (IL-6) cloning expression

    ASJC Scopus subject areas

    • Immunology
    • General Veterinary

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