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Deciphering adaptor specificity in GFL‐dependent RET‐mediated proliferation and neurite outgrowth
Author(s) -
Gustin Jason A.,
Yang Mao,
Johnson Eugene M.,
Milbrandt Jeffrey
Publication year - 2007
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2007.04624.x
Subject(s) - glial cell line derived neurotrophic factor , neurite , gdnf family of ligands , biology , signal transducing adaptor protein , microbiology and biotechnology , proto oncogene proteins c ret , neurotrophic factors , receptor tyrosine kinase , proto oncogene tyrosine protein kinase src , tyrosine kinase , signal transduction , growth factor , receptor , cancer research , genetics , in vitro
Glial cell derived neurotrophic factor (GDNF)‐dependent receptor tyrosine kinase RET activity is required for proper development of the nervous system and genitourinary tract. Loss‐of‐function mutations in RET are associated with enteric nervous system abnormalities (Hirschsprung disease) and renal deficits (Potter’s syndrome), whereas activating mutations lead to hereditary cancer syndromes (multiple endocrine neoplasia type 2A and type 2B). RET activation is crucial for the proper regulation of a variety of cellular processes including cell migration, proliferation and neurite outgrowth. By analyzing a series of RET mutants we found that Y1062 was critical for stimulating GDNF‐mediated proliferation as well as proliferation stimulated by GDNF‐independent oncogenic forms of RET. Studies using small interfering RNA driven by lentivirus to knock‐down expression of particular adaptor proteins that interact with RET phospho‐Y1062, demonstrated that only Src‐homology 2 and growth factor receptor binding protein 2 were necessary for RET‐mediated proliferation by wild type and oncogenic forms of RET. Interestingly, we discovered that Y1062 was also required for GDNF‐stimulated neurite outgrowth. However, small interfering RNAs to either Src‐homology 2 or growth factor receptor binding protein 2 or a panel of other adaptor proteins known to interact with RET Y1062 were incapable of blocking GDNF‐stimulated neurite formation, indicating that differential use of intracellular adaptors is responsible for regulating alternative RET‐stimulated cellular events such as proliferation versus a differentiation response like neurite outgrowth.