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Sequence, expression and function of an mRNA encoding a soluble form of the human interleukin-6 receptor (sIL-6R)

  • J. A. Lust(corresponding author)
    ,
  • D. F. Jelinek
    ,
  • K. A. Donovan
    ,
  • L. A. Frederick
    ,
  • B. K. Huntley
    ,
  • J. K. Braaten
*Corresponding author for this work
  • Mayo Clinic Rochester, MN
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Soluble receptors have been shown to be potent immunomodulators of their respective ligands. Since IL-6 is a central growth factor for myeloma cells, as sIL-6R may modulate IL-6 activity. We have previously reported a novel IL-6R mRNA from myeloma cells that exhibits a 94-nt deletion of the entire transmembrane domain from codons 356 (G-TG) to 387 (AG-G). The transmembrane domain deletion results in a shift in the translational reading frame with the insertion of 10 new amino acids followed by a stop codon. Sequence analysis shows the ligand-binding domain of the sIL-6R to be identical to that of the membrane-bound IL-6R up to the transmembrane domain deletion. The sIL-6R cDNA was expressed in QT-6 fibroblasts and PA-1 ovarian cells using the expression vector pCDM8. Supernates were immunoprecipitated with anti-IL-6R antibody and cells transfected with the sIL-6R cDNA produced a single band with a molecular weight of 50-55 kDa. This molecular weight corresponds to the size of the sIL-6R protein observed in normal human urine. Supernates were collected from mock or sIL-6R transfected PA-1 cells after 48 hours and assayed for their ability to stimulate or suppress the growth of an IL-6 dependent cell line, ANBL-6. Soluble IL-6R alone had no effect on the growth of the ANBL-6 cells. However, the growth of ANBL-6 cells by sIL-6R was potentiated in the presence of IL-6 and could be blocked by anti-IL-6 antibody. The above results suggest that, in the presence of IL-6, sIL-6R associates with gp130 leading to signal transduction and cell growth.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 199-206 (8 pages)

Journal (Volume, Issue Number)

Current topics in microbiology and immunology (Volume 194)

Publication milestones

  • Published - 1994

Publication status

Published - 1994

ISSN

0070-217X

Publication IDs

  • Scopus: 0028035051
  • PubMed: 7895493

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Scopus
citations
Fractional count
1
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0.14
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6
Fractional count
0.86
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1
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1

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Citation count
20
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12