Defective Transcytosis of APP and Lipoproteins in Human iPSC-Derived Neurons with Familial Alzheimer’s Disease Mutations

Cell Reports

Jessica E. Young¹  Elizabeth A. Roberts¹  Sol M. Reyna¹  Julia A. Callender¹  Mariah Dunlap¹  Rik Van Der Kant¹  Lawrence S.B. Goldstein¹  Grace Woodruff¹ 

[1] Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093, USA;

关键词: Alzheimer’s disease;    iPSC;    FAD;    APP;    PS1;    transcytosis;    endocytosis;   

DOI  :  10.1016/j.celrep.2016.09.034

来源: DOAJ

【 摘 要 】

We investigated early phenotypes caused by familial Alzheimer’s disease (fAD) mutations in isogenic human iPSC-derived neurons. Analysis of neurons carrying fAD PS1 or APP mutations introduced using genome editing technology at the endogenous loci revealed that fAD mutant neurons had previously unreported defects in the recycling state of endocytosis and soma-to-axon transcytosis of APP and lipoproteins. The endocytosis reduction could be rescued through treatment with a β-secretase inhibitor. Our data suggest that accumulation of β-CTFs of APP, but not Aβ, slow vesicle formation from an endocytic recycling compartment marked by the transcytotic GTPase Rab11. We confirm previous results that endocytosis is affected in AD and extend these to uncover a neuron-specific defect. Decreased lipoprotein endocytosis and transcytosis to the axon suggest that a neuron-specific impairment in endocytic axonal delivery of lipoproteins and other key materials might compromise synaptic maintenance in fAD.

【 授权许可】

Unknown