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Research Article Free access | 10.1172/JCI116839

Interleukin-6 functions as an intracellular growth factor in hairy cell leukemia in vitro.

B Barut, D Chauhan, H Uchiyama, and K C Anderson

Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115.

Find articles by Barut, B. in: JCI | PubMed | Google Scholar

Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115.

Find articles by Chauhan, D. in: JCI | PubMed | Google Scholar

Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115.

Find articles by Uchiyama, H. in: JCI | PubMed | Google Scholar

Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115.

Find articles by Anderson, K. in: JCI | PubMed | Google Scholar

Published November 1, 1993 - More info

Published in Volume 92, Issue 5 on November 1, 1993
J Clin Invest. 1993;92(5):2346–2352. https://doi.org/10.1172/JCI116839.
© 1993 The American Society for Clinical Investigation
Published November 1, 1993 - Version history
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Abstract

The role of interleukin-6 (IL-6) in the growth of B cell derived hairy cell leukemia (HCL) was characterized. Purified hairy cells (HCs) did not increase DNA synthesis in vitro in response to exogenous IL-6; however, they expressed IL-6 receptor (IL-6R) mRNA and bound directly fluorochrome labeled IL-6. IL-6 mRNA was not detectable in tumor cells by Northern blotting, but was evident using PCR amplification. Although intracytoplasmic IL-6 protein was not demonstrable, HCs did secrete low levels of IL-6. Neutralizing antibody to IL-6 did not inhibit HC DNA synthesis. Since tumor necrosis factor (TNF) is a growth factor for HCL, we determined whether the TNF effect could be IL-6-mediated. TNF markedly augmented in vitro DNA synthesis by HCs. TNF did not alter IL-6R expression or IL-6 binding; however, IL-6 mRNA and IL-6 protein were detectable after 3-d culture of HCs with TNF. In addition, IL-6 secretion by HCs was markedly augmented by TNF. Finally, although neither IL-6 nor anti-IL-6 antibody altered TNF-induced DNA synthesis by HCs, IL-6 antisense oligonucleotide inhibited TNF-induced DNA synthesis and IL-6 secretion by HCs. Therefore, IL-6 does not directly affect the growth of HCL, but rather mediates TNF-induced DNA synthesis via an intracytoplasmic mechanism.

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