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Article
Nature Neuroscience  3, 1085 - 1090 (2000)
doi:10.1038/80598

Reduction of endogenous transforming growth factors bold beta prevents ontogenetic neuron death

Kerstin Krieglstein1, Sandra Richter2, Lilla Farkas2, Norbert Schuster1, Nicole Dünker1, Ronald W. Oppenheim3 & Klaus Unsicker2

1  Department of Anatomy, Medical Faculty, University of Saarland at Homburg/Saar, Building 61, D-66421 Homburg/Saar , Germany

2  Department of Neuroanatomy, Interdisciplinary Center for Neuroscience, University of Heidelberg, INF 307, D-69120 Heidelberg, Germany

3  Neuroscience Program and Department of Neurobiology and Anatomy, Wake Forest University School of Medicine, Winston Salem, North Carolina 27157, USA

Correspondence should be addressed to Kerstin Krieglstein ankkri@med-rz.uni-sb.de
We show that following immunoneutralization of endogenous transforming growth factors beta (TGF-beta) in the chick embryo, ontogenetic neuron death of ciliary, dorsal root and spinal motor neurons was largely prevented, and neuron losses following limb bud ablation were greatly reduced. Likewise, preventing TGF-beta signaling by treatment with a TbetaR-II fusion protein during the period of ontogenetic cell death in the ciliary ganglion rescued all neurons that normally die. TUNEL staining revealed decreased numbers of apoptotic cells following antibody treatment. Exogenous TGF-beta rescued the TGF-beta-deprived phenotype. We conclude that TGF-beta is critical in regulating ontogenetic neuron death as well as cell death following neuronal target deprivation.

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Nature Neuroscience
ISSN: 1097-6256
EISSN: 1546-1726
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