Characterization of a multicomponent receptor for GDNF

• DOI: 10.1038/382080a0
• Publication Date: 2003-08-12T02:05:06Z
• Authors: James J. S. Treanor; Laurie Goodman; Frederic de Sauvage; Donna M. Stone; Kris T. Poulsen; Claus D. Beck; Christa Gray; Mark P. Armanini; Richard A. Pollock; Franz Hefti; Heidi S. Phillips; Audry Goddard; Mark W. Moore; Anna Buj-Bello; Alun M. Davies; Naoya Asai; Masahide Takahashi; Richard Vandlen; Christopher E. He...; Arnon Rosenthal
• Keywords: Proto-Oncogene Proteins c-ret

Glial-cell-line-derived neurotrophic factor (GDNF) is a potent survival factor for central and peripheral neurons, and is essential for the development of kidneys and the enteric nervous system. Despite the potential clinical and physiological importance of GDNF, its mechanism of action is unknown. Here we show that physiological responses to GDNF require the presence of a novel glycosyl-phosphatidylinositol (GPI)-linked protein (designated GDNFR-alpha) that is expressed on GDNF-responsive cells and binds GDNF with a high affinity. We further demonstrate that GDNF promotes the formation of a physical complex between GDNFR-alpha and the orphan tyrosin kinase receptor Ret, thereby inducing its tyrosine phosphorylation. These findings support the hypothesis that GDNF uses a multi-subunit receptor system in which GDNFR-alpha and Ret function as the ligand-binding and signalling components, respectively.