Overlapping and distinct actions of the neurotrophins BDNF, NT-3, and NT-4/5 on cultured dopaminergic and GABAergic neurons of the ventral mesencephalon

• Published in: The Journal of neuroscience Vol. 14; no. 1; pp. 335 - 347
• Main Authors: Hyman, C, Juhasz, M, Jackson, C, Wright, P, Ip, NY, Lindsay, RM
• Format: Journal Article
• Language: English
• Published: Washington, DC Soc Neuroscience 01.01.1994; Society for Neuroscience
• Subjects: Animals; Biological and medical sciences; Brain-Derived Neurotrophic Factor; Cell physiology; Cells, Cultured; Dopamine - metabolism; Fundamental and applied biological sciences. Psychology; gamma-Aminobutyric Acid - metabolism; Mesencephalon - cytology; Mesencephalon - drug effects; Mesencephalon - metabolism; Molecular and cellular biology; Nerve Growth Factors - pharmacology; Nerve Tissue Proteins - pharmacology; Neurons - drug effects; Neurons - metabolism; Neurotrophin 3; Rats; Receptor Protein-Tyrosine Kinases - metabolism; Receptor, trkC; Receptors, Growth Factor - metabolism; Responses to growth factors, tumor promotors, other factors; Substantia Nigra - metabolism; Tissue Distribution; Neurotrophin; Vertebrata; Mammalia; Rat; Rodentia; Central nervous system; Dopaminergic neuron; Brain derived neurotrophic factor; In vitro; Survival; Gabaergic neurone; Brain (vertebrata)
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/JNEUROSCI.14-01-00335.1994

The neurotrophins brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), and neurotrophin-4/5 (NT-4/5) were compared for their effects in promoting the survival and/or regulation of expression of phenotypic markers of dopaminergic and GABAergic neurons in cultures derived from embryonic rat ventral mesencephalon. Dopaminergic neuron number and phenotypic expression were monitored by tyrosine hydroxylase (TH) immunocytochemistry, and measurement of high-affinity dopamine uptake activity and dopamine content, respectively. High-affinity GABA uptake, glutamic acid decarboxylase (GAD) activity, and endogenous GABA content were used to detect GABAergic neurons. Seven days of treatment with either BDNF or NT-3 resulted in dose-dependent increases in the number of TH-positive neurons, with maximal responses of 3-fold and 2.3-fold, respectively. Dopamine uptake activity and dopamine content were similarly increased. The effects of BDNF and NT-3 on dopamine uptake activity showed no additivity. NT-4/5 treatment elicited the greatest increase (7-fold) in the number of TH-positive neurons, as well as a 2.6-fold increase in dopamine content. In marked contrast to BDNF or NT-3, NT-4/5 had no effect on dopamine uptake capacity. BDNF, NT-3, or NT-4/5 also produced dose-dependent elevations of 2-3-fold in GABA uptake activity. These effects were not additive. GAD activity was increased by BDNF (1.8-fold) and NT-3 (threefold) treatment, but not by NT-4/5, whereas GABA content was increased to a similar extent by all three neurotrophins. NGF had no effect on any of the parameters measured in this study. Northern analyses indicated that the mRNAs encoding TrkB and TrkC, the functional high-affinity receptors for BDNF and NT-4/5, and NT-3, respectively, are expressed in the substantia nigra of adult rat brain, as well as in cultures of developing ventral mesencephalon. Taken together, our results indicate that BDNF and NT-3 have broadly similar effects in promoting the survival and differentiated phenotype of both dopaminergic and GABAergic neurons of the developing substantia nigra. Although BDNF and NT-4/5 are thought to act through the same high-affinity receptor, TrkB, it is evident that these two neurotrophins have distinct as well as overlapping actions toward mesencephalic dopaminergic or GABAergic neurons.