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Molecular and Cellular Biology, August 2008, p. 4851-4861, Vol. 28, No. 15
0270-7306/08/$08.00+0 doi:10.1128/MCB.02178-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.


Department of Immunology and Cell Biology, Research Centre Borstel, D-23845 Borstel, Germany,1 Department of Dermatology, University Hospital Schleswig-Holstein, Campus Lübeck, University of Lübeck, D-23538 Lübeck, Germany2
Received 9 December 2007/ Returned for modification 16 February 2008/ Accepted 19 May 2008
While it is well appreciated that receptors for secreted cytokines transmit ligand-induced signals, little is known about additional roles for cytokine receptor components in the control of ligand transport and secretion. Here, we show that interleukin-15 (IL-15) translocation into the endoplasmic reticulum occurs independently of the presence of IL-15 receptor
(IL-15R
). Subsequently, however, IL-15 is transported through the Golgi apparatus only in association with IL-15R
and then is secreted. This intracellular IL-15/IL-15R
complex already is formed in the endoplasmic reticulum and, thus, enables the further trafficking of complexed IL-15 through the secretory pathway. Just transfecting IL-15R
in cells, which transcribe but normally do not secrete IL-15, suffices to induce IL-15 secretion. Thus, we provide the first evidence of how a cytokine is chaperoned through the secretory pathway by complexing with its own high-affinity receptor and show that IL-15/IL-15R
offers an excellent model system for the further exploration of this novel mechanism for the control of cytokine secretion.
Published ahead of print on 27 May 2008.
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