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. 1998 Dec 1;18(23):9835–9844. doi: 10.1523/JNEUROSCI.18-23-09835.1998

Fig. 2.

Fig. 2.

Preservation of punctate staining for presynaptic terminals. Cultured hippocampal neurons were incubated in the absence (A, B) or presence (C,D) of 50 μm NMDA for 15 min before double-labeling for F-actin (A, C) or for the synaptic vesicle marker synapsin-1 (B,D). Even while F-actin hot spots were lost, punctate staining for nerve terminals was preserved. Scale bar, 10 μm.