Abstract | OBJECTIVES: Brain imaging studies have implicated white matter dysfunction in the pathophysiology of both bipolar disorder (BD) and schizophrenia (SCZ). However, the contribution of axons to white matter pathology in these disorders is not yet understood. Maintenance of neuronal function is dependent on the active transport of biological material, including synaptic proteins, along the axon. In this study, the expression of six proteins associated with axonal transport of synaptic cargoes was quantified in postmortem samples of prefrontal white matter in subjects with BD, those with SCZ, and matched controls, as a measure of axonal dysfunction in these disorders. METHODS: RESULTS:
Protein expression of β- tubulin, kinesin-1, DISC1, synaptotagmin, and SNAP-25 was significantly lower in subjects with BD compared to controls. Levels of axon-associated proteins were also lower in subjects with SCZ, but failed to reach statistical significance. CONCLUSIONS: These data provide evidence for deficits in axon-associated proteins in prefrontal white matter in BD. Findings are suggestive of decreased axonal density or dysregulation of axonal function in this disorder.
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Authors | Li Shao, Khashayar Golbaz, William G Honer, Clare L Beasley |
Journal | Bipolar disorders
(Bipolar Disord)
Vol. 18
Issue 4
Pg. 342-51
(06 2016)
ISSN: 1399-5618 [Electronic] Denmark |
PMID | 27218831
(Publication Type: Journal Article)
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Copyright | © 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. |
Chemical References |
- KIF5B protein, human
- Synaptosomal-Associated Protein 25
- Tubulin
- Synaptotagmins
- Kinesins
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Topics |
- Adult
- Axons
(metabolism)
- Bipolar Disorder
(metabolism, pathology)
- Female
- Humans
- Kinesins
(metabolism)
- Male
- Middle Aged
- Prefrontal Cortex
(metabolism, pathology)
- Schizophrenia
(metabolism, pathology)
- Statistics as Topic
- Synaptosomal-Associated Protein 25
(metabolism)
- Synaptotagmins
(metabolism)
- Tubulin
(metabolism)
- White Matter
(metabolism, pathology)
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