The activation and subsequent proliferation of peripheral T cells requires
the engagement of the T cell and a cytokine receptor, typically the IL-2 or
IL-4 receptors. Critical to understanding the regulation of peripheral T c
ells is the knowledge of the unique contributions of each receptor to full
T cell activation and cell cycle progression. Mice deficient in Stat5a and
Stat5b have demonstrated the essential role that these highly related prote
ins play in cell cycle progression following peripheral T cell activation.
Here we demonstrate that activation of the Stat5 proteins by tyrosine phosp
horylation is uniquely contributed by cytokine receptor signaling and speci
fically does not occur through the T cell receptor complex.