Tubulin tyrosination regulates synaptic function and is disrupted in Alzheimer's disease

Microtubules play fundamental roles in the maintenance of neuronal processes and in synaptic function and plasticity. While dynamic microtubules are mainly composed of tyrosinated tubulin, long-lived microtubules contain detyrosinated tubulin, suggesting that the tubulin tyrosination/detyrosination cycle is a key player in the maintenance of microtubule dynamics and neuronal homeostasis, conditions that go awry in neurodegenerative diseases. In the tyrosination/detyrosination cycle, the C-terminal tyrosine of alpha-tubulin is removed by tubulin carboxypeptidases and re-added by tubulin tyrosine ligase (TTL). Here we show that TTL heterozygous mice exhibit decreased tyrosinated microtubules, reduced dendritic spine density and both synaptic plasticity and memory deficits. We further report decreased TTL expression in sporadic and familial Alzheimer's disease, and reduced microtubule dynamics in human neurons harbouring the familial APP-V717I mutation. Finally, we show that synapses visited by dynamic microtubules are more resistant to oligomeric amyloid-beta peptide toxicity and that expression of TTL, by restoring microtubule entry into spines, suppresses the loss of synapses induced by amyloid-beta peptide. Together, our results demonstrate that a balanced tyrosination/detyrosination tubulin cycle is necessary for the maintenance of synaptic plasticity, is protective against amyloid-beta peptide-induced synaptic damage and that this balance is lost in Alzheimer's disease, providing evidence that defective tubulin retyrosination may contribute to circuit dysfunction during neurodegeneration in Alzheimer's disease. Peris, Parato, Qu et al. demonstrate that tubulin tyrosine ligase (TTL) is reduced in Alzheimer's disease and that TTL hemizygous mice show memory impairment and reduced synaptic integrity. Tubulin retyrosination by TTL protects against A beta-induced synaptic damage by promoting microtubule entry into dendritic spines.

Automated summary

Microtubules are important for neuronal processes, synaptic function, and plasticity. The balance between tubulin tyrosination and detyrosination is crucial for maintaining microtubule dynamics and neuronal homeostasis. This study reveals that decreased tubulin tyrosine ligase expression is associated with Alzheimer's disease and leads to memory impairment and reduced synaptic integrity. Restoring microtubule entry into dendritic spines through tubulin retyrosination can protect against amyloid-beta peptide-induced synaptic damage.