4.7 Article

Interleukin 11 signaling in 3T3-L1 adipocytes

Journal

JOURNAL OF CELLULAR PHYSIOLOGY
Volume 202, Issue 1, Pages 160-166

Publisher

WILEY
DOI: 10.1002/jcp.20100

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Funding

  1. NIDDK NIH HHS [DK55169] Funding Source: Medline

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Intuleukin 11 (IL-11) is an anti-inflammatory cytokine with receptors located on most cell types and tissues throughout the body. Its anti-inflammatory properties are mediated through suppression of cytokine synthesis, in large part by prevention of NF-kappaB activation. As adipose tissue synthesizes and secretes cytokines involved in establishing insulin resistance and due to the ability of IL-11 to suppress cytokine synthesis, we initiated an investigation to determine the signal transduction pathways initiated by IL-11 in adipose tissue. Using the 3T3-L1 adipocyte cell culture model we demonstrate the rapid activation of the p44/42MAP kinase, P13-kinase, and STATs 1 and 3. Activation of MAP kinase is demonstrated to lead to the downstream activation of p90 RSK (ribosomal S6 kinase) as well as ATF-1 and CREB. P13-kinase appears to activate the downstream target of p70 S6 kinase resulting in phosphorylation of ribosomal protein S6. STAT phosphorylation appears to be initiated through P13-kinase and to a lesser degree through p44/42 MAP kinase. These studies demonstrate the activation of three major signaling pathways and support a role for IL-11 in the regulation of both transcription and protein synthesis in fully differentiated adipocytes. (C) 2004 Wiley-Liss, Inc.

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