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. 2010 Nov 29;5(11):e15108. doi: 10.1371/journal.pone.0015108

Figure 2. Widespread synaptic degeneration in the striatum of young (2 month old) wild-type, but not heterozygous WldS or homozygous WldS mice, 3 days after cortical lesion.

Figure 2

Representative electron micrographs of striatal synapses at low power (A) and higher power (B) from a young wild-type mouse (top panel), heterozygous WldS mouse (middle panel) and homozygous WldS mouse (bottom panel). Asterisks indicate degenerating synaptic profiles (identified principally by their electron dense cytoplasm) and arrows indicate healthy (i.e. non-degenerating) synaptic profiles. Degenerating synapses were readily identified in wild-type mice, occasionally observed in heterozygous WldS mice and rarely observed in homozygous WldS mice. However, the morphological appearance of degenerating synapses was indistinguishable between the different genotypes, suggesting that synapses in mice expressing the WldS gene ultimately degenerate by the same mechanism as in wild-type mice, albeit after a delay. Scale bars; A = 1 µm, B = 0.5 µm.