| Literature DB >> 33615987 |
Marijn Kuijpers1, Volker Haucke1,2.
Abstract
Neurons are long-lived cells that communicate via release of neurotransmitter at specialized contacts termed synapses. The maintenance of neuronal health and the regulation of synaptic function requires the efficient removal of damaged or dispensable proteins and organelles from synapses. How macroautophagy/autophagy contributes to neuronal and synaptic protein turnover, and what its main physiological substrates are in healthy neurons is largely unknown. We have now shown that loss of neuronal autophagy facilitates presynaptic neurotransmission by controlling the axonal endoplasmic reticulum and, thereby, axonal and synaptic calcium homeostasis.Entities:
Keywords: Autophagy; SV protein; calcium; endoplasmic reticulum; er-phagy; neurotransmission; reticulophagy; ryanodine receptor; synapse
Mesh:
Year: 2021 PMID: 33615987 PMCID: PMC8078701 DOI: 10.1080/15548627.2021.1893569
Source DB: PubMed Journal: Autophagy ISSN: 1554-8627 Impact factor: 16.016