Signal Transducer and Activator of Transcription (STATs) are important mediators of cytokine and growth factor-induced signal transduction, STAT5A and STAT5B have been shown to play a role in survival and proliferation of hematopoietic cells both in vitro and in viro and to contribute to the growth and viability of cells transformed by the TEL-JAK2 oncoprotein, In this study, we investigated the molecular mechanisms by which constitutively active STAT5 proteins induce cell proliferation and survival of Ba/F3 cell lines expressing either dominant positive STAT5A or STAT5B variants or TEL-JAK2 or TEL-ABL fusion proteins. Our results showed that active STAT5 constitutively interacted with p85, the regulatory subunit of the PT 3-kinase, A constitutive activity of the PI 3-kinase/Akt pathway was observed in these cells and required for their cell cycle progression. In contrast, while activity of the PI 3-kinase/Akt pathway was required for survival of Ba/F3 cells expressing the constitutively active forms of STAT5A or STAT5B, it was dispensable for cells transformed by TEL-JAK2 or TEL-ABL fusion proteins, suggesting that additional survival pathways take place in these transformed cells.