4.8 Article

GFR alpha-mediated localization of RET to lipid rafts is required for effective downstream signaling, differentiation, and neuronal survival

期刊

NEURON
卷 25, 期 3, 页码 611-623

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CELL PRESS
DOI: 10.1016/S0896-6273(00)81064-8

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  1. NATIONAL INSTITUTE ON AGING [R01AG013729, R01AG013730] Funding Source: NIH RePORTER
  2. NIA NIH HHS [AG-13730, AG-13729] Funding Source: Medline

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The GDNF family ligands (GFLs: GDNF, neurturin, persephin, and artemin) signal through RET and a glycosyl-phosphatidylinositol (GPI)-anchored coreceptor (GFR alpha 1-alpha 4) that binds ligand with high affinity and provides specificity. The importance of the GPI anchor is not fully understood; however, GPI-linked proteins cluster into lipid rafts, structures that may represent highly specialized signaling organelles. Here, we report that GPI-anchored GFR alpha 1 recruits RET to lipid rafts after GDNF stimulation and results in RET/Src association. Disruption of RET localization using either transmembrane-anchored or soluble GFR alpha 1 results in RET phosphorylation, but GDNF-induced intracellular signaling events are markedly attenuated as are neuronal differentiation and survival responses. Therefore, proper membrane localization of RET via interaction with a raft-localized, GPI-linked coreceptor is of fundamental importance in GFL signaling.

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