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Blood, Vol. 95 No. 8 (April 15), 2000: pp. 2715-2718

BRIEF REPORT


Constitutive activation of LIL-Stat in adult T-cell leukemia cells

Junichi Tsukada, Yoko Toda, Masahiro Misago, Yoshiya Tanaka, Philip E. Auron, and Sumiya Eto

From the First Department of Internal Medicine, School of Medicine, and School of Health Sciences, University of Occupational and Environmental Health, Kitakyushu, Japan; and The New England Baptist Bone & Joint Institute, Beth Israel Deaconess Medical Center and Department of Medicine, Harvard Medical School, Boston, MA.

The activation status of a recently identified STAT (signal transducers and activators of transcription) factor, LIL-Stat (lipopolysaccharide [LPS]/IL-1-inducible Stat) in adult T-cell leukemia (ATL) cells was investigated by electrophoretic mobility shift assays using nuclear extracts of leukemic cells from 7 patients with ATL and a GAS (gamma interferon activation site)-like element termed LILRE (LPS/IL-1-responsive element), which is found in the human prointerleukin 1beta (IL1B) gene. Spontaneous DNA binding of LIL-Stat was observed in all ATL cells examined. However, in normal human peripheral lymphocytes, DNA binding of LIL-Stat was detected only after stimulation with IL-1. These results demonstrated that LIL-Stat is constitutively activated in ATL cells. Furthermore, our transient transfection studies using LILRE chloramphenicol acetyltransferase (CAT) reporters argue that LIL-Stat in ATL cells functions as a transcriptional activator through binding to the LILRE in the IL1B gene.


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