Cell type-specific roles of Jak3 in IL-2-induced proliferative signal transduction
Creators
- 1. Department of Pathology, New York University School of Medicine, 550 First Avenue, MSB-126, New York, NY 10016 (United States)
Description
Binding of interleukin-2 (IL-2) to its specific receptor induces activation of two members of Jak family protein tyrosine kinases, Jak1 and Jak3. An IL-2 receptor (IL-2R)-reconstituted NIH 3T3 fibroblast cell line proliferates in response to IL-2 only when hematopoietic lineage-specific Jak3 is ectopically expressed. However, the mechanism of Jak3-dependent proliferation in the fibroblast cell line is not known. Here, I showed that Jak3 expression is dispensable for IL-2-induced activation of Jak1 and Stat proteins and expression of nuclear proto-oncogenes in the IL-2R-reconstituted fibroblast cell line. Jak3 expression markedly enhanced these IL-2-induced signaling events. In contrast, Jak3 expression was essential for induction of cyclin genes involved in the G1-S transition. These data suggest a critical role of Jak3 in IL-2 signaling in the fibroblast cell line and may provide further insight into the cell type-specific mechanism of cytokine signaling
Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2007.01.067;
- PII
- S0006-291X(07)00119-2;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 354
- Journal Issue
- 3
- Journal Page Range
- p. 825-829
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 39008542
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- CELL PROLIFERATION; FIBROBLASTS; ONCOGENES; PHOSPHOTRANSFERASES; RECEPTORS; TYROSINE
- Descriptors DEC
- AMINO ACIDS; ANIMAL CELLS; CARBOXYLIC ACIDS; CONNECTIVE TISSUE CELLS; ENZYMES; GENES; HYDROXY ACIDS; MEMBRANE PROTEINS; ORGANIC ACIDS; ORGANIC COMPOUNDS; PHOSPHORUS-GROUP TRANSFERASES; PROTEINS; SOMATIC CELLS; TRANSFERASES
Optional Information
- Copyright
- Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.