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Dual control of neurite outgrowth by STAT3 and MAP kinase in PC12 cells stimulated with interleukin‐6
Author(s) -
Ihara Sayoko,
Nakajima Koichi,
Fukada Toshiyuki,
Hibi Masahiko,
Nagata Satoshi,
Hirano Toshio,
Fukui Yasuhisa
Publication year - 1997
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/16.17.5345
Subject(s) - biology , neurite , microbiology and biotechnology , dual (grammatical number) , stat3 , mitogen activated protein kinase , kinase , signal transduction , biochemistry , in vitro , art , literature
IL‐6 induces differentiation of PC12 cells pretreated with nerve growth factor (NGF). We explored the signals required for neurite outgrowth of PC12 cells by using a series of mutants of a chimeric receptor consisting of the extracellular domain of the granulocyte‐colony stimulating factor (G‐CSF) receptor and the cytoplasmic domain of gp130, a signal‐transducing subunit of the IL‐6 receptor. The mutants incapable of activating the MAP kinase cascade failed to induce neurite outgrowth. Consistently, a MEK inhibitor, PD98059, inhibited neurite outgrowth, showing that activation of the MAP kinase cascade is essential for the differentiation of PC12 cells. In contrast, a mutation that abolished the ability to activate STAT3 did not inhibit, but rather stimulated neurite outgrowth. This mutant did not require NGF pretreatment for neurite outgrowth. Dominant‐negative STAT3s mimicked NGF pretreatment, and NGF suppressed the IL‐6‐induced activation of STAT3, supporting the idea that STAT3 might regulate the differentiation of PC12 cells negatively. These results suggest that neurite outgrowth of PC12 cells is regulated by the balance of MAP kinase and STAT3 signal transduction pathways, and that STAT3 activity can be regulated negatively by NGF.