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Resolution: standard / high Figure 8.
Tau pathology in TDP-43M337V mice. Immunohistochemistry of the cortices of (A) TDP-43M337V and (B) TDP-43WT mice showed elevated levels of phosphorylated tau (CP13) in both TDP-43M337V and TDP-43WT mice compared to (C) NT mice. (D) Western blotting of brain lysates from NT, TDP-43
M337V and TDP-43WT mice probed with CP13 antibody showed increases in murine tau phosphorylation at serine
residues 202 in both lines of TDP-43 transgenic mice. Staining with tau-1 antibody
showed reduced dephosphorylated tau levels in both lines of TDP-43 transgenic mice
when compared to NT mice. Staining with antibody tau-5 showed that overall tau levels
were equivalent across non-transgenic and transgenic mice. There was a dramatic increase
of phospho-(Ser) PKC substrate in both TDP-43 transgenic lines indicating PKC activation
that was not present in NT mice. Scale bars: 50 μM in A, B and C.
Xu et al. Molecular Neurodegeneration 2011 6:73 doi:10.1186/1750-1326-6-73 |