Temporal sequences of synapse disintegration triggered by afferent axon transection, time-lapse imaging study of presynaptic and postsynaptic molecules

4Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.

Abstract

Traumatic brain injury (TBI) is one of the major causes of death and disability. Multiple animal models have been developed to explore therapeutic targets for TBI. However, heterogeneity of pathophysiology obstructs discovery of therapeutic targets. To facilitate understanding of TBI pathophysiology, each element of neuronal and glial responses should be studied separately. We focused on synapse remodeling which plays an important role in recovery from TBI and developed a new method, afferent elimination, for analyzing synapse remodeling after selective damage to presynaptic axons by mechanical transection in culture of mouse hippocampal neurons. Afferent elimination can induce various events related to synapse remodeling and we could determine their temporal orders and find relationships between them. Specifically, loss of presynaptic sites preceded loss of postsynaptic sites and spines. Some of the postsynaptic sites initially located inside spines showed translocation toward dendritic shafts. These translocation events started after the loss of contacting presynaptic sites. Also, these events could be blocked or delayed by NMDA receptor inhibition. Taken together, these findings suggest that postsynaptic changes occur in afferent elimination are NMDA dependent and imply that these NMDAdependent events underlie synaptic remodeling of TBI.

Cite

CITATION STYLE

APA

Cho, T., Kashiwagi, Y., & Okabe, S. (2019). Temporal sequences of synapse disintegration triggered by afferent axon transection, time-lapse imaging study of presynaptic and postsynaptic molecules. ENeuro, 6(5). https://doi.org/10.1523/ENEURO.0459-18.2019

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free