Characterization of a Novel Interleukin-1 Receptor Antagonist from Sheep ().

J Interferon Cytokine Res

Key Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonosis / College of Veterinary Medicine, Jilin University, Changchun, China.

Published: May 2020

AI Article Synopsis

  • Interleukin-1 receptor antagonist (IL-1Ra) blocks IL-1β from activating its receptors, but it does not trigger any cellular responses.
  • Researchers identified the full-length cDNA of the IL-1Ra gene in sheep and submitted it to GenBank, showing a unique structure that includes UTR regions and encodes for a specific protein.
  • The study found that the OaIL-1Ra protein is widely present in various organs and is particularly abundant in the liver and spleen, with its expression significantly increasing in sheep's white blood cells during bacterial infections, indicating its role in immune responses.

Article Abstract

Interleukin-1 receptor antagonist (IL-1Ra) is an antagonist of IL-1β binding IL-1β receptors but does not induce intracellular responses or signal transduction. In this study, the full-length complementary DNA (cDNA) of the gene () was identified from sheep () using rapid amplification of cDNA ends PCR and submitted to GenBank with the accession number KC425613. The cDNA comprised an open reading frame of 525 bp encoding a protein of 19765.8 Da, a 5'-untranslated region (UTR) of 27 bp, and a 3'-UTR of 676 bp with a poly(A) tail. Recombinant OaIL-1Ra with bioactivity was expressed in a prokaryotic expression system, and a monoclonal antibody against native OaIL-1Ra was prepared. Through Western blot analyses, the OaIL-1Ra protein was widely expressed in lung, heart, spleen, liver, kidney, muscle, intestine, lymphonodi, rumen, and white blood cells, with the highest levels in liver and spleen. The expression of OaIL-1Ra in primary cultured white blood cells of sheep were highly induced in a time-dependent manner when challenged with different bacteria. These results implied that is associated with immune responses during bacterial infections.

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http://dx.doi.org/10.1089/jir.2019.0182DOI Listing

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