Author:
Alata Milvia,Piazza Valeria,Jaramillo-Restrepo Carla,Eguibar Jose R.,Cortes Carmen,Hernandez Victor H.
Abstract
AbstractHypomyelination with atrophy of the basal ganglia and cerebellum is a recently described tubulinopathy caused by a mutation in the tubulin beta 4a isoform, expressed in oligodendrocytes. The taiep rat is the only spontaneous tubulin beta 4a mutant available for the study of this pathology. We aimed to identify the effects of the tubulin mutation on freshly collected, unstained samples of the central white matter of taiep rats using second harmonic generation microscopy. Cytoskeletal differences between the central white matter of taiep rats and control animals were found. Nonlinear emissions from the processes and somata of oligodendrocytes in tubulin beta 4a mutant rats were consistently detected, in the shape of elongated structures and cell-like bodies, which were never detected in the controls. This signal represents the second harmonic trademark of the disease. The tissue was also fluorescently labeled and analyzed to corroborate the origin of the nonlinear signal. Besides enabling the description of structural and molecular aspects of H-ABC, our data open the door to the diagnostic use of nonlinear optics in the study of neurodegenerative diseases, with the additional advantage of a label-free approach that preserves tissue morphology and vitality.
Funder
Consejo Nacional de Ciencia y Tecnología
Publisher
Springer Science and Business Media LLC
Reference52 articles.
1. Curiel, J. et al. TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes. Hum. Mol. Genet. 26, 4506–4518 (2017).
2. Simons, C. et al. A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum. Am. J. Hum. Genet. 92, 767–773 (2013).
3. Garduno-Robles, A. et al. MRI features in a rat model of H-ABC tubulinopathy. Front. Neurosci. 14, 555 (2020).
4. Erro, R. et al. H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?. Mov. Disord. Off. J. Mov. Disord. Soc. 30, 828–833 (2015).
5. van der Knaap, M. S. et al. New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellum. Am. J. Neuroradiol. 23, 1466–1474 (2002).
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