Distinct functions for anterograde and retrograde sorting of SORLA in amyloidogenic processes in the brain

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  • Sonya B. Dumanis, Max Delbrueck Center for Molecular Medicine
  • ,
  • Tilman Burgert, Max Delbrueck Center for Molecular Medicine
  • ,
  • Safak Caglayan, Max Delbrueck Center for Molecular Medicine
  • ,
  • Annette Füchtbauer
  • Ernst Martin Füchtbauer
  • Vanessa Schmidt, Max Delbrueck Center for Molecular Medicine
  • ,
  • Thomas E. Willnow, Max Delbrueck Center for Molecular Medicine

SORLA is a neuronal sorting receptor implicated both in sporadic and familial forms of AD. SORLA reduces the amyloidogenic burden by two mechanisms, either by rerouting internalized APP molecules from endosomes to the trans-Golgi network (TGN) to prevent proteolytic processing or by directing newly produced Aβ to lysosomes for catabolism. Studies in cell lines suggested that the interaction of SORLA with cytosolic adaptors retromer and GGA is required for receptor sorting to and from the TGN. However, the relevance of anterograde or retrograde trafficking forSORLAactivity in vivo remained largely unexplored. Here, we generated mouse models expressing SORLA variants lacking binding sites for GGA or retromer to query this concept in the brain. Disruption of retromer binding resulted in a retrograde-sorting defect with accumulation of SORLA in endosomes and depletion from the TGN, and in an overall enhanced APP processing. In contrast, disruption of the GGA interaction did not impact APP processing but caused increased brain Aβ levels, a mechanism attributed to a defect in anterograde lysosomal targeting of Aβ. Our findings substantiated the significance of adaptormediated sorting for SORLA activities in vivo, and they uncovered that anterograde and retrograde sorting paths may serve discrete receptor functions in amyloidogenic processes.

OriginalsprogEngelsk
TidsskriftJournal of Neuroscience
Vol/bind35
Nummer37
Sider (fra-til)12703-12713
Antal sider11
ISSN0270-6474
DOI
StatusUdgivet - 2015

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