TY - JOUR
T1 - Environment Matters: Synaptic Properties of Neurons Born in the Epileptic Adult Brain Develop to Reduce Excitability.
AU - Jakubs, Katherine
AU - Nanobashvili, Avtandil
AU - Bonde, Sara
AU - Ekdahl Clementson, Christine
AU - Kokaia, Zaal
AU - Kokaia, Merab
AU - Lindvall, Olle
N1 - The information about affiliations in this record was updated in December 2015.
The record was previously connected to the following departments: Stem Cell Center (013041110), Restorative Neurology (0131000160), Neurology, Lund (013027000), Epilepsy Center (013230801)
PY - 2006
Y1 - 2006
N2 - Neural progenitors in the adult dentate gyrus continuously produce new functional granule cells. Here we used whole-cell patch-clamp recordings to explore whether a pathological environment influences synaptic properties of new granule cells labeled with a GFP-retroviral vector. Rats were exposed to a physiological stimulus, i.e., running, or a brain insult, i.e., status epilepticus, which gave rise to neuronal death, inflammation, and chronic seizures. Granule cells formed after these stimuli exhibited similar intrinsic membrane properties. However, the new neurons born into the pathological environment differed with respect to synaptic drive and short-term plasticity of both excitatory and inhibitory afferents. The new granule cells formed in the epileptic brain exhibited functional connectivity consistent with reduced excitability. We demonstrate a high degree of plasticity in synaptic inputs to adult-born new neurons, which could act to mitigate pathological brain function.
AB - Neural progenitors in the adult dentate gyrus continuously produce new functional granule cells. Here we used whole-cell patch-clamp recordings to explore whether a pathological environment influences synaptic properties of new granule cells labeled with a GFP-retroviral vector. Rats were exposed to a physiological stimulus, i.e., running, or a brain insult, i.e., status epilepticus, which gave rise to neuronal death, inflammation, and chronic seizures. Granule cells formed after these stimuli exhibited similar intrinsic membrane properties. However, the new neurons born into the pathological environment differed with respect to synaptic drive and short-term plasticity of both excitatory and inhibitory afferents. The new granule cells formed in the epileptic brain exhibited functional connectivity consistent with reduced excitability. We demonstrate a high degree of plasticity in synaptic inputs to adult-born new neurons, which could act to mitigate pathological brain function.
U2 - 10.1016/j.neuron.2006.11.004
DO - 10.1016/j.neuron.2006.11.004
M3 - Article
SN - 0896-6273
VL - 52
SP - 1047
EP - 1059
JO - Neuron
JF - Neuron
IS - 6
ER -