TY - JOUR
T1 - Constitutively active STAT5 variants induce growth and survival of hematopoietic cells through a PI 3-kinase/Akt dependent pathway
AU - Santos, Susana Constantino Rosa
AU - Lacronique, Virginie
AU - Bouchaert, Isabelle
AU - Monni, Richard
AU - Bernard, Olivier
AU - Gisselbrecht, Sylvie
AU - Gouilleux, Fabrice
N1 - Funding Information:
The authors would like to thank Drs Tosio Kitamura for providing the STAT5A1*6 and STAT5B 1*6 cDNAs, P Mayeux for the Ba/F3Epo-R cell, S Fichelson for the human erythroid progenitors and the Faculdade de Farm-ácia at Lisbon. This work was supported by ARC (Association de Recherche contre le Cancer) and Fonda-tion de France. SC Rosa Santos is supported by Praxis XXI.
PY - 2001/4/19
Y1 - 2001/4/19
N2 - 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 vivo 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 PI 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.
AB - 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 vivo 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 PI 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.
KW - PI 3-kinase
KW - STAT5
KW - Survival
KW - TEL-JAK2
UR - http://www.scopus.com/inward/record.url?scp=0035912097&partnerID=8YFLogxK
U2 - 10.1038/sj.onc.1204308
DO - 10.1038/sj.onc.1204308
M3 - Article
C2 - 11360192
AN - SCOPUS:0035912097
SN - 0950-9232
VL - 20
SP - 2080
EP - 2090
JO - Oncogene
JF - Oncogene
IS - 17
ER -