Accepted Preprint (first posted online 28 February 2011)

    GDNF and protection of adult central catecholaminergic neurons

    1. Jose Lopez-Barneo
    1. A Pascual, Hospital Universitario Virgen del Rocio/CSIC/Universidad de Sevilla, Instituto de Biomedicina de Sevilla (IBiS), Seville, Spain
    2. M Hidalgo-Figueroa, Hospital Universitario Virgen del Rocio/CSIC/Universidad de Sevilla, Instituto de Biomedicina de Sevilla (IBiS), Seville, Spain
    3. R Gomez-Diaz, Hospital Universitario Virgen del Rocio/CSIC/Universidad de Sevilla, Instituto de Biomedicina de Sevilla (IBiS), Seville, Spain
    4. J Lopez-Barneo, Instituto de Biomedicina de Sevilla, Edificio de Laboratorios, 2a planta, Hospital Universitario Virgen del Rocío, Avenida Manuel Siurot s/n, 41013-Sevilla, Spain,
    1. Correspondence: Alberto Pascual, Email: apascual{at}ibis-sevilla.es

    Abstract

    Neurotrophic factors are small proteins necessary for neuron survival and maintenance of phenotype. They are considered as promising therapeutic tools for neurodegenerative diseases. The glial cell line-derived neurotrophic factor (GDNF) protects catecholaminergic cells from toxic insults, thus its potential therapeutic applicability in Parkinson's disease has been intensely investigated. In recent years, there have been major advances in the analysis of GDNF signaling pathways in peripheral neurons and embryonic dopamine mesencephalic cells. However, the actual physiologic role of GDNF in maintaining catecholaminergic central neurons during adulthood is only starting to be unraveled, and the mechanisms whereby GDNF protects central brain neurons are poorly known. Here, we review the current knowledge of GDNF expression, signaling, and function in adult brain, with special emphasis on the genetic animal models with deficiency in the GDNF-dependent pathways.

    • Received 31 August 2010
    • Revision received 23 February 2011
    • Accepted 28 February 2011
    • Accepted Preprint first posted online on 28 February 2011

    This Article

    1. J Mol Endocrinol JME-10-0125
    1. Abstract
    2. All Versions of this Article:
      1. JME-10-0125v1
      2. 46/3/R83 most recent