|
Resolution: standard / high Figure 1.
NMDAR activation controls accumulation of synapsin at developing excitatory presynaptic
terminals. (A, B) Immunofluorescence images of synapsin in a control neuron (A) and a neuron treated
with APV to block NMDAR activation (B). Fluorescence intensity is pseudo-colored according
to the indicated scale. Scale bar: 10 μm. (C) APV treatment decreases accumulation of synapsin at developing presynaptic terminals.
To ensure that presynaptic puncta were synaptic, analysis was limited to synapsin
puncta that overlapped with PSD95. (D) APV similarly decreased the apparent size of synapsin puncta. (E) APV did not significantly decrease the density of synapsin puncta. Data are presented
as mean ± standard error of the mean, normalized to the control mean, and the number
of puncta (C-D) and images (E) measured are indicated on each bar. *, significant
difference (P-values are indicated in the figure). (F) Immunoblot demonstrating that overall levels of synapsin were unchanged by APV treatment.
(G) Quantification of synapsin integrated density from immunoblotting. The small difference
in intensity was not significant (P = 0.28).
Sceniak et al. Neural Development 2012 7:8 doi:10.1186/1749-8104-7-8 |