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The microtubule-modulating drug Epothilone D alters dendritic spine morphology in a mouse model of mild traumatic brain injury
Citation
Chuckowree, JA and Zhu, Z and Brizuela, MD and Lee, KM and Blizzard, CA and Dickson, TC, The microtubule-modulating drug Epothilone D alters dendritic spine morphology in a mouse model of mild traumatic brain injury, Frontiers in Cellular Neuroscience, 12 Article 223. ISSN 1662-5102 (2018) [Refereed Article]
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Copyright Statement
Copyright 2018 The Authors Licensed under Creative Commons Attribution 4.0 International (CC BY 4.0) https://creativecommons.org/licenses/by/4.0/
DOI: doi:10.3389/fncel.2018.00223
Abstract
Microtubule dynamics underpin a plethora of roles involved in the intricate development, structure, function, and maintenance of the central nervous system. Within the injured brain, microtubules are vulnerable to misalignment and dissolution in neurons and have been implicated in injury-induced glial responses and adaptive neuroplasticity in the aftermath of injury. Unfortunately, there is a current lack of therapeutic options for treating traumatic brain injury (TBI). Thus, using a clinically relevant model of mild TBI, lateral fluid percussion injury (FPI) in adult male Thy1-YFPH mice, we investigated the potential therapeutic effects of the brain-penetrant microtubule-stabilizing agent, epothilone D. At 7 days following a single mild lateral FPI the ipsilateral hemisphere was characterized by mild astroglial activation and a stereotypical and widespread pattern of axonal damage in the internal and external capsule white matter tracts. These alterations occurred in the absence of other overt signs of trauma: there were no alterations in cortical thickness or in the number of cortical projection neurons, axons or dendrites expressing YFP. Interestingly, a single low dose of epothilone D administered immediately following FPI (and sham-operation) caused significant alterations in the dendritic spines of layer 5 cortical projection neurons, while the astroglial response and axonal pathology were unaffected. Specifically, spine length was significantly decreased, whereas the density of mushroom spines was significantly increased following epothilone D treatment. Together, these findings have implications for the use of microtubule stabilizing agents in manipulating injury-induced synaptic plasticity and indicate that further study into the viability of microtubule stabilization as a therapeutic strategy in combating TBI is warranted.
Item Details
| Item Type: | Refereed Article |
|---|---|
| Keywords: | traumatic brain injury, fluid percussion injury, neuroplasticity, microtubule stabilization, epothilone D, dendritic spine, cortical projection neuron, mushroom spine |
| Research Division: | Biomedical and Clinical Sciences |
| Research Group: | Neurosciences |
| Research Field: | Neurology and neuromuscular diseases |
| Objective Division: | Health |
| Objective Group: | Clinical health |
| Objective Field: | Clinical health not elsewhere classified |
| UTAS Author: | Chuckowree, JA (Dr Jyoti Chuckowree) |
| UTAS Author: | Zhu, Z (Mr Zhendan Zhu) |
| UTAS Author: | Brizuela, MD (Ms Mariana Brizuela) |
| UTAS Author: | Lee, KM (Miss Clara Lee) |
| UTAS Author: | Blizzard, CA (Dr Catherine Blizzard) |
| UTAS Author: | Dickson, TC (Professor Tracey Dickson) |
| ID Code: | 128145 |
| Year Published: | 2018 |
| Web of Science® Times Cited: | 14 |
| Deposited By: | Menzies Institute for Medical Research |
| Deposited On: | 2018-09-05 |
| Last Modified: | 2019-03-04 |
| Downloads: | 128 View Download Statistics |
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