Is activation of GDNF/RET signaling the answer for successful treatment of Parkinson's disease? A discussion of data from the culture dish to the clinic

James A. Conway, Edgar R. Kramer*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

8 Downloads (Pure)

Abstract

The neurotrophic signaling of glial cell line-derived neurotrophic factor (GDNF) with its canonical receptor, the receptor tyrosine kinase RET, coupled together with the GDNF family receptor alpha 1 is important for dopaminergic neuron survival and physiology in cell culture experiments and animal models. This prompted the idea to try GDNF/RET signaling as a therapeutic approach to treat Parkinson's disease with the hallmark of dopaminergic cell death in the substantia nigra of the midbrain. Despite several clinical trials with GDNF in Parkinson's disease patients, which mainly focused on optimizing the GDNF delivery technique, benefits were only seen in a few patients. In general, the endpoints did not show significant improvements. This suggests that it will be helpful to learn more about the basic biology of this fascinating but complicated GDNF/RET signaling system in the dopaminergic midbrain and about recent developments in the field to facilitate its use in the clinic. Here we will refer to the latest publications and point out important open questions in the field.

Original languageEnglish
Pages (from-to)1462-1467
Number of pages6
JournalNeural Regeneration Research
Volume17
Issue number7
DOIs
Publication statusPublished - 10 Dec 2021

ASJC Scopus subject areas

  • Developmental Neuroscience

Keywords

  • Clinical trials
  • Dopaminergic neurons
  • GFRα1
  • Glial cell line-derived neurotrophic factor
  • Gut-brain axis
  • Nedd4
  • Parkin
  • Parkinson's disease
  • RET
  • α-synuclein

Fingerprint

Dive into the research topics of 'Is activation of GDNF/RET signaling the answer for successful treatment of Parkinson's disease? A discussion of data from the culture dish to the clinic'. Together they form a unique fingerprint.

Cite this