electron microscopy;
post-embedding immunogold;
postsynaptic density;
scaffolding protein;
signal transduction;
D O I:
10.1093/cercor/bhi070
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Prefrontal cortical functioning depends on D1 family receptors and their complex signal transduction cascade, including protein phosphatase-1 (PP1). Three PP1 isoforms are prominent in the brain: PP1 alpha, PP1 beta and PP1 gamma 1. PP1 localization by a variety of scaffolding proteins is critical for dopamine-mediated modulation of glutamatergic neurotransmission. We have quantified the subcellular distribution of each isoform in primate prefrontal cortex using immunoelectron microscopy. All three are found in spines, dendrites, axon terminals, axons and glia. However, PP1 alpha and PP1 gamma 1 labeling is enriched in spines, whereas PP1 beta label is enriched in dendrites. Using post-embedding immunogold labeling, we further examined the distribution of PP1 alpha and PP1 gamma 1 within spines. PP1 gamma 1 is highly and specifically concentrated in the postsynaptic density (PSD) of these spines, while PP1 alpha is enriched in the PSD but also found subjacent to the PSD in moderate amounts. Thus, PP1 isoforms are heterogeneously distributed in the cortical neuropil and within spines. These results suggest that each PP1 isoform has access to a different set of substrates and, furthermore, they demonstrate that the composition of signal transduction proteins varies in different parts of the neuron and even in different regions of a dendritic spine in the primate PFC.