Author/Authors :
Guido Hansen، نويسنده , , Timothy R. Hercus، نويسنده , , Barbara J. McClure، نويسنده , , Frank C. Stomski، نويسنده , , Mara Dottore، نويسنده , , Jason Powell، نويسنده , , Hayley Ramshaw، نويسنده , , Joanna M. Woodcock، نويسنده , , Yibin Xu، نويسنده , , Mark Guthridge، نويسنده , , William J. McKinstry، نويسنده , , Angel F. Lopez، نويسنده , , Michael W. Parker، نويسنده ,
Abstract :
Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a pleiotropic cytokine that controls the production and function of blood cells, is deregulated in clinical conditions such as rheumatoid arthritis and leukemia, yet offers therapeutic value for other diseases. Its receptors are heterodimers consisting of a ligand-specific α subunit and a βc subunit that is shared with the interleukin (IL)-3 and IL-5 receptors. How signaling is initiated remains an enigma. We report here the crystal structure of the human GM-CSF/GM-CSF receptor ternary complex and its assembly into an unexpected dodecamer or higher-order complex. Importantly, mutagenesis of the GM-CSF receptor at the dodecamer interface and functional studies reveal that dodecamer formation is required for receptor activation and signaling. This unusual form of receptor assembly likely applies also to IL-3 and IL-5 receptors, providing a structural basis for understanding their mechanism of activation and for the development of therapeutics.
