The tyrosine phosphatase CD45 dephosphorylates the negative regulatory tyrosine of the Src family kinase Lck and plays a positive role in TCR signaling. In this study we demonstrate a negative regulatory role for CD45 in CD44 signaling leading to actin rearrangement and cell spreading in activated thymocytes and T cells. In BW5147 T cells, CD44 ligation led to CD44 and Lck clustering, which generated a reduced tyrosine phosphorylation signal in CD45+ T cells and a more sustained, robust tyrosine phosphorylation signal in CD45− T cells. This signal resulted in F-actin ring formation and round spreading in the CD45+ cells and polarized, elongated cell spreading in CD45− cells. The enhanced signal in the CD45− cells was consistent with enhanced Lck Y394 phosphorylation compared with the CD45+ cells where CD45 was recruited to the CD44 clusters. This enhanced Src family kinase-dependent activity in the CD45− cells led to PI3K and phospholipase C activation, both of which were required for elongated cell spreading. We conclude that CD45 induces the dephosphorylation of Lck at Y394, thereby preventing sustained Lck activation and propose that the amplitude of the Src family kinase-dependent signal regulates the outcome of CD44-mediated signaling to the actin cytoskeleton and T cell spreading.