Biology Open (Aug 2012)

The intracellular portion of GITR enhances NGF-promoted neurite growth through an inverse modulation of Erk and NF-κB signalling

  • Laura McKelvey,
  • Humberto Gutierrez,
  • Giuseppe Nocentini,
  • Sean J. Crampton,
  • Alun M. Davies,
  • Carlo R. Riccardi,
  • Gerard W. O’keeffe

DOI
https://doi.org/10.1242/bio.20121024
Journal volume & issue
Vol. 1, no. 10
pp. 1016 – 1023

Abstract

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Summary NF-κB transcription factors play a key role in regulating the growth of neural processes in the developing PNS. Although several secreted proteins have been shown to activate NF-κB to inhibit the growth of developing sympathetic neurons, it is unknown how the endogenous level of NF-κB activity present in these neurons is restricted to allow neurite growth to occur during their normal development. Here we show that activation of the glucocorticoid-induced tumour necrosis factor receptor (GITR) inhibits NF-κB activation while promoting the activation of Erk in developing sympathetic neurons. Conversely, inhibition of GITR results in an increase in NF-κB dependent gene transcription and a decrease in Erk activation leading to a reduction in neurite growth. These findings show that GITR signalling can regulate the extent of sympathetic neurite growth through an inverse modulation of Erk and NF-κB signalling, which provides an optimal environment for NGF-promoted growth.

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