fig3

Deregulation of mitochondrial reverse electron transport alters the metabolism of reactive oxygen species and NAD<sup>+</sup>/NADH and presents a therapeutic target in Alzheimer's disease

Figure 3. Effect of CPT on disease phenotypes in FAD iPSC derived neurons. (A) Immunostainings and data quantification showing the effect of CPT treatment on mOC78 positive beta-amyloid aggregates in control iPSC neurons and FAD iPSC neurons treated with vehicle or CPT; (B) Immunostainings and data quantification showing the effect of CPT treatment on CP13 positive p-tau signals in control iPSC neurons and FAD iPSC neurons treated with vehicle or CPT; (C) Immunostainings and data quantification showing the effect of CPT treatment on total tau signals in control iPSC neurons and FAD iPSC neurons treated with vehicle or CPT; (D) Immunostainings and data quantification showing the effect of CPT treatment on Rab5 positive early endosome signals in control iPSC neurons and FAD iPSC neurons treated with vehicle or CPT. ***P < 0.001, ns: not significant, in Student’s t-test or one-way ANOVA test. CPT: CPT2008, 6-chloro-3-(2,4-dichloro-5-methoxyphenyl)-2-mecapto-7-methoxyquinazolin-4(3H)-one; FAD: familial Alzheimer’s disease; iPSC: induced pluripotent stem cell.

Ageing and Neurodegenerative Diseases
ISSN 2769-5301 (Online)

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Portico

All published articles will be preserved here permanently:

https://www.portico.org/publishers/oae/