Lymphocytes expressing the common gamma chain can form functional receptors for these cytokine proteins, which transmit
signals from one cell to another and direct programs of
cellular differentiation.
Ligands The γc chain partners with other
ligand-specific receptors to direct lymphocytes to respond to
cytokines including
IL-2,
IL-4,
IL-7,
IL-9,
IL-15 and
IL-21.
Signaling IL2RG has been shown to
interact with
Janus kinase 3. IL2RG plays a critical role in lymphocyte signal transduction in response to
IL-4,
IL-7,
IL-9,
IL-21,
IL-15, and
IL-2. Once either
IL4-Rα,
IL-7Rα,
IL-9Rα,
IL-21Rα,
IL-2R or
IL-15R has bound to their respective ligands, IL2RG is quickly recruited and forms a
heterodimer with the cytoplasmic tail of the opposing receptor. After the heterodimer has formed, IL2RG then activates
JAK3, and the opposing receptor activates
JAK1. JAK1 and JAK3 then
phosphorylate both IL2RG and the opposing receptor's cytoplasmic tail. This phosphorylation allows for IL-2RG and its opposing receptor to recruit a
STAT protein. JAK3 and JAK1 subsequently phosphorylate the recruited STAT, allowing the STAT to form a dimer or
tetramer with other phosphorylated STAT proteins. Finally, these dimer or STATs translocate to the nucleus, bind STAT motifs within the nuclear DNA, and induce transcription within specific genes. ==Clinical significance==