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    Nat Neurosci. 2008 Feb;11(2):135-42. Epub 2008 Jan 6.

    NGF-promoted axon growth and target innervation requires GITRL-GITR signaling.

    O'Keeffe GW, Gutierrez H, Pandolfi PP, Riccardi C, Davies AM.

    School of Biosciences, Biomedical Building, Museum Avenue, Cardiff, CF10 3US, UK.

    Nerve growth factor (NGF) has an important role in regulating sympathetic neuron survival and target field innervation during development. Here we show that glucocorticoid-induced tumor necrosis factor receptor-related protein (GITR), a member of the TNF superfamily, and its ligand (GITRL) are co-expressed in mouse sympathetic neurons when their axons are innervating their targets under the influence of target-derived NGF. In culture, GITRL enhanced NGF-promoted neurite growth from neonatal sympathetic neurons, and preventing GITR-GITRL interaction in these neurons or knocking down GITR inhibited NGF-promoted neurite growth without affecting neuronal survival. Tnfrsf18(-/-) (Gitr) neonates have reduced sympathetic innervation density in vivo compared with Gitr(+/+) littermates. GITR activation is required for the phosphorylation of extracellular signal-regulated kinases 1 and 2 by NGF that is necessary for neurite growth. Our results reveal a previously unknown signaling loop in developing sympathetic neurons that is crucial for NGF-dependent axon growth and target innervation.

    PMID: 18176559 [PubMed - indexed for MEDLINE]

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