α-Synuclein facilitates endocytosis by elevating the steady-state levels of phosphatidylinositol 4,5-bisphosphate

• Published in: The Journal of biological chemistry Vol. 295; no. 52; p. 18076
• Main Authors: Schechter, Meir, Atias, Merav, Abd Elhadi, Suaad, Davidi, Dana, Gitler, Daniel, Sharon, Ronit
• Format: Journal Article
• Language: English
• Published: United States 25.12.2020
• Subjects: α-Synuclein; Clathrin-mediated endocytosis; clathrin; phosphorylated AP2; endocytosis; synapse; synaptic vesicles cycling; alpha-synuclein (α-synuclein); phosphoinositide; phosphoinositides
• ISSN: 1083-351X

α-Synuclein (α-Syn) is a protein implicated in the pathogenesis of Parkinson's disease (PD). It is an intrinsically disordered protein that binds acidic phospholipids. Growing evidence supports a role for α-Syn in membrane trafficking, including, mechanisms of endocytosis and exocytosis, although the exact role of α-Syn in these mechanisms is currently unclear. Here we investigate the associations of α-Syn with the acidic phosphoinositides (PIPs), phosphatidylinositol 4,5-bisphosphate (PI(4,5)P ) and phosphatidylinositol 3,4-bisphosphate (PI(3,4)P ). Our results show that α-Syn colocalizes with PIP and the phosphorylated active form of the clathrin adaptor protein 2 (AP2) at clathrin-coated pits. Using endocytosis of transferrin as an indicator for clathrin-mediated endocytosis (CME), we find that α-Syn involvement in endocytosis is specifically mediated through PI(4,5)P levels on the plasma membrane. In accord with their effects on PI(4,5)P levels, the PD associated A30P, E46K, and A53T mutations in α-Syn further enhance CME in neuronal and nonneuronal cells. However, lysine to glutamic acid substitutions at the KTKEGV repeat domain of α-Syn, which interfere with phospholipid binding, are ineffective in enhancing CME. We further show that the rate of synaptic vesicle (SV) endocytosis is differentially affected by the α-Syn mutations and associates with their effects on PI(4,5)P levels, however, with the exception of the A30P mutation. This study provides evidence for a critical involvement of PIPs in α-Syn-mediated membrane trafficking.