The Reelin Receptor ApoER2 is a Cargo for the Adaptor Protein Complex AP-4: Implications for Hereditary Spastic Paraplegia

Author:

Caracci Mario O.,Pizarro Héctor,Alarcón-Godoy Carlos,Fuentealba Luz M.,Farfán Pamela,Pace Raffaella De,Santibañez Natacha,Cavieres Viviana A.,Pástor Tammy P.,Bonifacino Juan S.,Mardones Gonzalo A.,Marzolo María-PazORCID

Abstract

ABSTRACTAdaptor protein complex 4 (AP-4) is a heterotetrameric complex that promotes protein export from thetrans-Golgi network. Mutations in each of the AP-4 subunits cause a complicated form of Hereditary Spastic Paraplegia (HSP). Herein, we report that ApoER2, a receptor in the Reelin signaling pathway, is a cargo of the AP-4 complex. We identify the motif ISSF/Y within the ApoER2 cytosolic domain as necessary for interaction with the canonical signal-binding pocket of the µ4 (AP4M1) subunit of AP-4.AP4E1-knock-out (KO) HeLa cells and hippocampal neurons fromAp4e1-KO mice display increased Golgi localization of ApoER2. Furthermore, hippocampal neurons fromAp4e1-KO mice andAP4M1-KO human iPSC-derived cortical i3Neurons exhibit reduced ApoER2 protein expression. Analyses of biosynthetic transport of ApoER2 reveal differential post-Golgi trafficking of the receptor, with lower axonal distribution in KO compared to wild-type neurons, indicating a role of AP-4 and the ISSF/Y motif in the axonal localization of ApoER2. Finally, analyses of Reelin signaling in mouse hippocampal and human cortical KO neurons show that AP4 deficiency causes no changes in Reelin-dependent activation of the AKT pathway and only mild changes in Reelin-induced dendritic arborization, but reduces Reelin-induced ERK phosphorylation, CREB activation, and Golgi deployment. Altogether, this work establishes ApoER2 as a novel cargo of the AP-4 complex, suggesting that defects in the trafficking of this receptor and in the Reelin signaling pathway could contribute to the pathogenesis of HSP caused by mutations in AP-4 subunits.

Publisher

Cold Spring Harbor Laboratory

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