Light microscopic identification and immunocytochemical characterization of glutamatergic synapses in brain sections
- 14 October 2005
- journal article
- research article
- Published by Wiley in Journal of Comparative Neurology
- Vol. 492 (4) , 495-509
- https://doi.org/10.1002/cne.20743
Abstract
Presynaptic proteins are readily identified by light microscopic immunocytochemistry, but immunodetection of postsynaptic proteins in brain sections proves difficult. We performed immunofluorescent double labeling for the NR1 subunit of theN‐methyl‐D‐aspartate receptor (NMDAR) and the vesicular glutamate transporter 1 (VGLUT1). In material fixed with 4% paraformaldehyde, NMDAR staining in somatosensory cortex was restricted to the section surface, whereas presynaptic staining extended deeper into the tissue. Staining for postsynaptic proteins was enhanced in weakly fixed material and in tissue treated with pepsin, as previously reported, but tissue quality was impaired. Staining was also markedly enhanced, and without impairment of tissue quality, by treatment during perfusion with a mixture of inhibitors of proteases and the ubiquitin/proteosome system. We performed quantitative analysis of confocal images to study how immunostaining varies with depth into the tissue. Virtually all puncta immunopositive for VGLUT1 colocalized with synaptophysin puncta; these presynaptic puncta were most numerous 1–2 μm beneath the section surface. In contrast, puncta immunopositive for the NR1 subunit were most numerous at the surface, as were puncta immunopositive for the NR2 subunit, SynGAP, and CaMKII. Punctate staining for all postsynaptic proteins, but not presynaptic markers, was substantially enhanced in material pretreated with antiproteolytic agents. The large majority of NR1‐positive puncta at the surface associated with VGLUT1 in this material are likely to represent synaptic contacts. Approximately eighty‐five percent of VGLUT1‐positive puncta in layers II–III of SI are associated with NR1‐positive puncta, and ∼80% are associated with NR2, SynGAP, and CaMKII. This approach may permit systematic analysis of the chemistry of glutamatergic synapses with light microscopic immunocytochemistry. J. Comp. Neurol. 492:495–509, 2005.Keywords
This publication has 70 references indexed in Scilit:
- Identification and Verification of Novel Rodent Postsynaptic Density ProteinsMolecular & Cellular Proteomics, 2004
- Targeting of calcium/calmodulin-dependent protein kinase IIBiochemical Journal, 2004
- Alterations in regional brain metabolism in genetic and pharmacological models of reduced NMDA receptor functionBrain Research, 2002
- The molecular basis of CaMKII function in synaptic and behavioural memoryNature Reviews Neuroscience, 2002
- Improved immunohistochemical detection of postsynaptically located PSD-95/SAP90 protein family by protease section pretreatment: A study in the adult mouse brainJournal of Comparative Neurology, 2000
- Colocalization of multiple GABAA receptor subtypes with gephyrin at postsynaptic sitesJournal of Comparative Neurology, 2000
- Expression of NR1, NR2A-D, and NR3 subunits of the NMDA receptor in the cerebral cortex and olfactory bulb of adult ratSynapse, 2000
- Synaptic localization of GABAA receptor subunits in the striatum of the ratJournal of Comparative Neurology, 2000
- Quantitative aspects of synaptogenesis in the rat barrel field cortex with special reference to GABA circuitryJournal of Comparative Neurology, 1996
- Targeted disruption of NMDA receptor 1 gene abolishes NMDA response and results in neonatal deathPublished by Elsevier ,1994