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Kinase suppressor of RAS (KSR) amplifies the differentiation signal provided by low concentrations 1,25‐dihydroxyvitamin D 3
Author(s) -
Wang Xuening,
Studzinski George P.
Publication year - 2004
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.10443
Subject(s) - microbiology and biotechnology , mapk/erk pathway , kinase , cellular differentiation , signal transduction , differentiation therapy , chemistry , biology , biochemistry , retinoic acid , acute promyelocytic leukemia , gene
The activity of kinase suppressor of ras (KSR), a kinase or a molecular scaffold upstream from Raf‐1, is involved in the MEK/ERK MAP kinase cascade which can signal cell growth, survival, or differentiation, depending on the cellular context. We provide evidence here that KSR is upregulated in HL60 cells undergoing differentiation induced by low (0.3–3 nM) concentrations of 1,25‐dihydroxyvitamin D 3 (1,25D 3 ), and an antisense oligo (AS), but not a sense oligo, to KSR inhibits this differentiation. The inhibition of differentiation by AS–KSR oligo was less apparent when the concentration of 1,25D 3 was increased, suggesting that at the higher concentrations of 1,25D 3 KSR is not essential for the signaling of the differentiated phenotype. The reduced differentiation of HL60 cells exposed to AS–KSR was paralleled by reduced phosphorylation of Raf‐1 Ser 259, and of p90RSK, used here as read‐out for MAPK cascade activity. Conversely, ectopic expression of Flag‐tagged wild type KSR potentiated the differentiation‐inducing effects of low concentrations of 1,25D 3 . Additional data suggest that the kinase activity of KSR is required for these effects, as transfection of a kinase inactive KSR construct did not significantly increase the 1,25D 3 ‐induced differentiation. Enzyme assays performed with KSR immunoprecipitated from 1,25D 3 ‐treated cells showed kinase activity when recombinant Raf‐1 was used as the substrate, but not when the 1,25D 3 ‐treated cells were pretreated with AS–KSR oligos. Taken together, these data suggest that KSR participates in signaling of monocytic differentiation by augmenting the strength of the signal transmitted through Raf‐1 to downstream targets. J. Cell. Physiol. 198: 333–342, 2004© 2003 Wiley‐Liss, Inc.