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The Journal of Neuroscience, December 1, 2000, 20(23):8597-8603
Growth/Differentiation Factor-15/Macrophage Inhibitory
Cytokine-1 Is a Novel Trophic Factor for Midbrain Dopaminergic
Neurons In Vivo
Jens
Strelau1,
Aideen
Sullivan2,
Martina
Böttner1,
Paul
Lingor1,
Elisabeth
Falkenstein3,
Clemens
Suter-Crazzolara1,
Dagmar
Galter1,
Jozsef
Jaszai1,
Kerstin
Krieglstein4, and
Klaus
Unsicker1
1 Neuroanatomy and Interdisciplinary Center for
Neurosciences, University of Heidelberg, D-69120 Heidelberg, Germany,
2 Department of Anatomy, University College, Cork,
Ireland, 3 Department of Clinical Pharmacology,
Faculty for Clinical Medicine, University of Heidelberg, D-68167
Mannheim, Germany, and 4 Department of Anatomy, University
of the Saarland, D-66421 Homburg, Germany
Transforming growth factor- s (TGF- s) constitute an expanding
family of multifunctional cytokines with prominent roles in development, cell proliferation, differentiation, and repair. We have
cloned, expressed, and raised antibodies against a distant member of
the TGF- s, growth/differentiation factor-15 (GDF-15). GDF-15 is
identical to macrophage inhibitory cytokine-1 (MIC-1). GDF-15/MIC-1
mRNA and protein are widely distributed in the developing and adult CNS
and peripheral nervous systems, including choroid plexus and CSF.
GDF-15/MIC-1 is a potent survival promoting and protective factor for
cultured and iron-intoxicated dopaminergic (DAergic) neurons cultured
from the embryonic rat midbrain floor. The trophic effect of
GDF-15/MIC-1 was not accompanied by an increase in cell proliferation
and astroglial maturation, suggesting that GDF-15/MIC-1 probably acts
directly on neurons. GDF-15/MIC-1 also protects 6-hydroxydopamine
(6-OHDA)-lesioned nigrostriatal DAergic neurons in vivo.
Unilateral injections of GDF-15/MIC-1 into the medial forebrain bundle
just above the substantia nigra (SN) and into the left ventricle (20 µg each) immediately before a 6-OHDA injection (8 µg) prevented
6-OHDA-induced rotational behavior and significantly reduced losses of
DAergic neurons in the SN. This protection was evident for at least 1 month. Administration of 5 µg of GDF-15/MIC-1 in the same paradigm
also provided significant neuroprotection. GDF-15/MIC-1 also promoted
the serotonergic phenotype of cultured raphe neurons but did not
support survival of rat motoneurons. Thus, GDF-15/MIC-1 is a novel
neurotrophic factor with prominent effects on DAergic and serotonergic
neurons. GDF-15/MIC-1 may therefore have a potential for the treatment
of Parkinson's disease and disorders of the serotonergic system.
Key words:
GDF-15/MIC-1; TGF- ; dopaminergic neurons; 6-OHDA; Parkinson's disease; neurotrophic factor
Copyright © 2000 Society for Neuroscience 0270-6474/00/20238597-07$05.00/0
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