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The JAK-STAT Signaling Pathway: Input and Output Integration
Author(s) -
Peter J. Murray
Publication year - 2007
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.178.5.2623
Subject(s) - socs3 , stat , jak stat signaling pathway , janus kinase 1 , cytokine receptor , suppressor of cytokine signaling 1 , signal transduction , suppressor of cytokine signalling , receptor , socs5 , biology , socs6 , microbiology and biotechnology , cytokine , janus kinase , socs2 , cancer research , stat3 , suppressor , immunology , gene , genetics , receptor tyrosine kinase
Universal and essential to cytokine receptor signaling, the JAK-STAT pathway is one of the best understood signal transduction cascades. Almost 40 cytokine receptors signal through combinations of four JAK and seven STAT family members, suggesting commonality across the JAK-STAT signaling system. Despite intense study, there remain substantial gaps in understanding how the cascades are activated and regulated. Using the examples of the IL-6 and IL-10 receptors, I will discuss how diverse outcomes in gene expression result from regulatory events that effect the JAK1-STAT3 pathway, common to both receptors. I also consider receptor preferences by different STATs and interpretive problems in the use of STAT-deficient cells and mice. Finally, I consider how the suppressor of cytokine signaling (SOCS) proteins regulate the quality and quantity of STAT signals from cytokine receptors. New data suggests that SOCS proteins introduce additional diversity into the JAK-STAT pathway by adjusting the output of activated STATs that alters downstream gene activation.

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