Fig. 1From: Morphological and transcriptomic analyses of stem cell-derived cortical neurons reveal mechanisms underlying synaptic dysfunction in schizophreniaDendritic spines and synapses in SCZ and CON cortical neurons. A,B Images of dendritic spines in SCZ and CON neurons, labeled with layer III marker CUX1 or layer V marker CTIP2 and MAP2—arrows point to representative spines. C Automated quantification of spine density in dendrites in CUX1 or CTIP2 neurons from seven CON and seven SCZ lines, with three replicates each (box and whisker plot min to max, p < 0.001, unpaired t-test with Welch’s correction). D,E Images of synaptic puncta in SCZ and CON neurons, labeled with layer III marker CUX1 or layer V marker CTIP2, MAP2, presynaptic marker Bassoon (red) and postsynaptic marker Homer (green)—arrows point to representative synaptic puncta with overlap of Bassoon and Homer. F Automated quantification of synaptic puncta in neurons from seven CON and seven SCZ lines. SCZ neurons showed significantly fewer synapses compared for both CUX1 and CTIP2 neurons (dot plots, mean + / − SEM, p < 0.001, unpaired t-test with Welch’s correction). Scale bar = 20μm. G Images of Ca++ imaging in CON and SCZ neurons before and after 30 mM KCl. Scale bar = 100μm. H Trace of Ca.++ fluorophore intensity before and after KCl. I Change in fluorescence intensity in cell bodies upon KCl exposure. SCZ neurons had lower increase in fluorescence intensity after KCl (mean + / − SEM, p < 0.001, Mann–Whitney U test)Back to article page