Constitutively Activated Jak-STAT Pathway in T Cells Transformed with HTLV-I

Thi‐Sau Migone(National Institutes of Health), Jian‐Xin Lin(National Institutes of Health), Anna Cereseto(National Cancer Institute), James C. Mulloy(National Cancer Institute), John J. O’Shea(National Institutes of Health), Genoveffa Franchini(National Cancer Institute), Warren J. Leonard(National Institutes of Health)
Science
July 7, 1995
Cited by 566

Abstract

Human T cell lymphotropic virus I (HTLV-I) is the etiological agent for adult T cell leukemia and tropical spastic paraparesis (also termed HTLV-I-associated myelopathy). HTLV-I-infected peripheral blood T cells exhibit an initial phase of interleukin-2 (IL-2)-dependent growth; over time, by an unknown mechanism, the cells become IL-2-independent. Whereas the Jak kinases Jak1 and Jak3 and the signal transducer and activator of transcription proteins Stat3 and Stat5 are activated in normal T cells in response to IL-2, this signaling pathway was constitutively activated in HTLV-I-transformed cells. In HTLV-I-infected cord blood lymphocytes, the transition from IL-2-dependent to IL-2-independent growth correlated with the acquisition of a constitutively activated Jak-STAT pathway, which suggests that this pathway participates in HTLV-I-mediated T cell transformation.


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