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. 2018 Jan 30;90(5):e380–e387. doi: 10.1212/WNL.0000000000004899

Figure 3. Colocalization of tau phosphorylated at threonine 175 (pThr175 tau) and tau phosphorylated at threonine 231 (pThr231 tau).

Figure 3

Hippocampal neurons in chronic traumatic encephalopathy (CTE) (upper panels) demonstrate colocalization of pThr175 tau and pThr231 tau. The presence of pathologic tau oligomers (T22 immunoreactivity) was colocalized to pThr231 tau-immunoreactive neurons in CTE (middle panels). Consistent with a role in activation of glycogen synthase kinase–3β (GSK3β) in inducing pathologic tau deposition, we observed the colocalization of pThr175tau with the active pGSK3β immunoreactivity (lower panel). Tissues were immunolabeled with rabbit anti-pThr175 tau, rabbit anti-pThr231 tau, rabbit anti-T22 antibody, and mouse anti-GSK3β pTyr216 antibody. For double-labeled tissue, red channel antibodies were labeled directly with Alexa Fluor 555. Scale bar = 5 μm.