Project Details
Projekt
Amphisome biogenesis couples synaptic autophagy to local protein synthesis
Applicants
Dr. Maria Andres-Alonso; Professor Dr. Eckart D. Gundelfinger; Professor Dr. Michael R. Kreutz
Subject Area
Molecular Biology and Physiology of Neurons and Glial Cells
Term
since 2021
Project identifier
Deutsche Forschungsgemeinschaft (DFG) - Project number 447288260
Amphisomes are hybrid organelles that result from the fusion of autophagosomes with late endosomes. In non-neuronal they are of transient nature and they rapidly undergo degradation. In previous work we found that in neurons amphisomes are endowed with signaling properties as a result of the incorporation of active TrkB receptors to autophagosomes. We showed that trafficking and signaling capabilities of amphisomes are controlled by SIPA1L2, a RapGAP protein that serves as a link to the dynein motor complex via its interaction with Snapin, and that it also regulates TrkB downstream signaling via Rap1 and ultimately ERK activation. Both features are regulated in a PKA-dependent manner, as PKA phosphorylation causes the stopover of the organelles at presynapses and the termination of SIPA1L2’s RapGAP activity which enables ERK activation at boutons. During Syntophagy’s first funding period we investigated how amphisomes are formed in neurons and the mechanisms leading to amphisome biogenesis. It turned out that amphisomes come to existence after synaptogenesis and that synaptic activity is the main driver for their biogenesis. Accordingly, we found that high-frequency stimulation causes the recruitment of autophagy proteins to boutons and the induction of synaptic autophagy at presynapses as well as amphisome biogenesis. Furthermore, our work revealed that bulk endosomes have an essential function as membrane donors supporting the formation of amphisomes, and that activation of AMPK at boutons is instrumental for amphisome biogenesis. Moreover, we showed that amphisome biogenesis regulates BDNF/TrkB-dependent local protein synthesis at boutons. Capitalizing on these findings, we will investigate which signaling mechanisms lead to the induction of synaptic autophagy, with particular focus on AMPK activation and downstream signaling and how this relates to the recruitment of autophagy proteins to the presynapse. Moreover, we aim to understand the role of bulk endosomes as membrane donors in amphisome formation and their role in activity-dependent local protein synthesis at the presynapse. Finally, we will investigate how amphisomes regulate the synthesis and degradation of presynaptic proteins and how amphisomes control the local mitochondrial function by enabling the translation of mitochondrial proteins.
DFG Programme
Research Units
