Abstract
Astrocytes promote the formation and function of excitatory synapses in the CNS. However, whether and how astrocytes modulate inhibitory synaptogenesis are essentially unknown. We asked whether astrocytes regulate the formation of inhibitory synapses between hippocampal neurons during maturation in vitro. Neuronal coculture with astrocytes or treatment with astrocyte-conditioned medium (ACM) increased the number of inhibitory presynaptic terminals, the frequency of miniature IPSCs, and the number and synaptic localization of GABA(A) receptor (GABA(A)R) clusters during the first 10 d in vitro. We asked whether neurotrophins, which are potent modulators of inhibitory synaptic structure and function, mediate the effects of astrocytes on inhibitory synapses. ACM from BDNF- or tyrosine receptor kinase B (TrkB)-deficient astrocytes increased inhibitory presynaptic terminals and postsynaptic GABA(A)R clusters in wild-type neurons, suggesting that BDNF and TrkB expression in astrocytes is not required for these effects. In contrast, although the increase in the number of inhibitory presynaptic terminals persisted, no increase was observed in postsynaptic GABA(A)R clusters after ACM treatment of hippocampal neurons lacking BDNF or TrkB. These results suggest that neurons, not astrocytes, are the relevant source of BDNF and are the site of TrkB activation required for postsynaptic GABA(A)R modulation. These data also suggest that astrocytes may modulate postsynaptic development indirectly by stimulating Trk signaling between neurons. Together, these data show that astrocytes modulate inhibitory synapse formation via distinct presynaptic and postsynaptic mechanisms.
Publication types
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Comparative Study
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Research Support, N.I.H., Extramural
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Analysis of Variance
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Animals
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Animals, Newborn
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Astrocytes / cytology
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Astrocytes / physiology*
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Biotinylation / methods
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Blotting, Western / methods
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Brain-Derived Neurotrophic Factor / physiology
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Cell Count / methods
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Cells, Cultured
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Coculture Techniques / methods
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Culture Media, Conditioned / pharmacology
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Electric Stimulation / methods
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Embryo, Mammalian
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Excitatory Postsynaptic Potentials / drug effects
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Excitatory Postsynaptic Potentials / physiology
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Excitatory Postsynaptic Potentials / radiation effects
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Gene Expression Regulation / drug effects
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Glial Fibrillary Acidic Protein / metabolism
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Hippocampus / cytology
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Immunoglobulin G / pharmacology
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Immunohistochemistry / methods
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In Situ Nick-End Labeling / methods
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Mice
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Mice, Knockout
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Microtubule-Associated Proteins / metabolism
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Nerve Growth Factors / pharmacology
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Neural Inhibition / drug effects
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Neural Inhibition / physiology*
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Neurons / cytology
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Neurons / physiology*
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Patch-Clamp Techniques / methods
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Presynaptic Terminals / drug effects
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Presynaptic Terminals / metabolism
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Rats
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Rats, Sprague-Dawley
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Receptor, trkA / deficiency
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Receptor, trkA / immunology
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Receptor, trkA / metabolism*
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Receptors, GABA-A / physiology*
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Synapses / drug effects
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Synapses / physiology*
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Synaptophysin / metabolism
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Time Factors
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Vesicular Glutamate Transport Protein 1 / metabolism
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Vesicular Inhibitory Amino Acid Transport Proteins / metabolism
Substances
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Brain-Derived Neurotrophic Factor
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Culture Media, Conditioned
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Glial Fibrillary Acidic Protein
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Immunoglobulin G
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MAP2 protein, rat
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Microtubule-Associated Proteins
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Nerve Growth Factors
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Receptors, GABA-A
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Slc32a1 protein, rat
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Synaptophysin
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Vesicular Glutamate Transport Protein 1
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Vesicular Inhibitory Amino Acid Transport Proteins
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Receptor, trkA