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The Journal of Neuroscience, July 1, 2000, 20(13):4992-5000

GFRalpha 1 Is Required for Development of Distinct Subpopulations of Motoneuron

A. Garcès1, G. Haase1, M. S. Airaksinen2, J. Livet1, P. Filippi1, and O. deLapeyrière1

1 Institut National de la Santé et de la Recherche Médicale (INSERM) U.382, Developmental Biology Institute of Marseille (Centre National de la Recherche Scientifique-INSERM-Université de la Méditerranée, AP de Marseille), Campus de Luminy, 13288 Marseille Cedex 09, France, and 2 Institute of Biotechnology, Viikki Biocenter, University of Helsinki, Helsinki FIN-00014, Finland

Glial cell-line derived neurotrophic factor (GDNF) and its relative neurturin (NTN) are potent trophic factors for motoneurons. They exert their biological effects by activating the RET tyrosine kinase in the presence of a glycosyl-phosphatidylinositol-linked co-receptor, either GFRalpha 1 or GFRalpha 2. By whole-mount in situ hybridization on embryonic mouse spinal cord, we demonstrate that whereas Ret is expressed by nearly all motoneurons, Gfra1 and Gfra2 exhibit complex and distinct patterns of expression. Most motoneurons purified from Gfra1 null mutant mice had lost their responsiveness to both GDNF and NTN. However, a minority of them (~25%) retained their ability to respond to both factors, perhaps because they express GFRalpha 2. Surprisingly, Gfra2-/- motoneurons showed normal survival responses to both GDNF and NTN. Thus, GFRalpha 1, but not GFRalpha 2, is absolutely required for the survival response of a majority of motoneurons to both GDNF and NTN. In accordance with the phenotype of the mutant motoneurons observed in culture we found the loss of distinct groups of motoneurons, identified by several markers, in the Gfra1-/- spinal cords but no gross defects in the Gfra2-/- mutant. During their natural programmed cell death period, motoneurons in the Gfra1-/- mutant mice undertook increased apoptosis. Taken together these findings support the existence of subpopulations of motoneuron with different trophic requirements, some of them being dependent on the GDNF family.

Key words: motoneuron subpopulations; motoneuron survival; neurotrophic factors; GDNF; NTN; Ret; Gfra1; Gfra2; in situ hybridization; mutant mice


Copyright © 2000 Society for Neuroscience  0270-6474/00/20134992-09$05.00/0


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