Retrograde propagation of GDNF-mediated signals in sympathetic neurons.

Mol Cell Neurosci

Division of Molecular Neurobiology, Department of Neuroscience, Karolinska Institute, 17177 Stockholm, Sweden.

Published: October 2004

AI Article Synopsis

  • GDNF family ligands are important for the survival and growth of certain neurons, working through specific receptors (GFR alpha and RET) to regulate signals that promote neuronal health.
  • Research using compartmentalized cultures of sympathetic neurons showed that adding GDNF to either the cell bodies or distal axons triggered local signaling, activating important downstream pathways such as AKT and ERK1/2.
  • GDNF addition to distal axons created a retrograde signal that enhanced neuron survival and outgrowth, with evidence of retrograde transport of GDNF and receptors to the cell bodies, but no forward signaling was detected.

Article Abstract

Glial cell line-derived neurotrophic factor (GDNF) family ligands are target-derived trophic factors for several neuronal subpopulations. They promote survival and neurite outgrowth through binding to specific members of the GDNF family receptor alpha (GFR alpha) and subsequent activation of the RET tyrosine kinase receptor. Using compartmentalized cultures of sympathetic neurons, we have studied the mechanism of GDNF retrograde signaling. Our results demonstrate the presence of GDNF receptors RET and GFR alpha 1 in the two cellular compartments, cell bodies and distal axons. Addition of GDNF to either compartment initiated local signaling, including activation of RET and its downstream effectors AKT and ERK1/2. Addition of GDNF to distal axons induced a retrograde signal leading to neuronal survival and neurite outgrowth. Retrograde signaling was associated with retrograde transport of radiolabeled GDNF and GFR alpha 1, as well as activation of RET and AKT, but not of ERK1/2, in cell bodies. No anterograde signal propagation or transport was observed. Our results suggest a general mechanism for retrograde signaling initiated at distal axons through tyrosine kinase receptors.

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Source
http://dx.doi.org/10.1016/j.mcn.2004.06.001DOI Listing

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