Abstract

Juvenile neuronal ceroid lipofuscinosis (JNCL, aka. juvenile Batten disease or CLN3 disease), a lethal pediatric neurodegenerative disease without cure, often presents with vision impairment and characteristic ophthalmoscopic features including focal areas of hyper-autofluorescence. In the associated research article “Loss of CLN3, the gene mutated in juvenile neuronal ceroid lipofuscinosis, leads to metabolic impairment and autophagy induction in retinal pigment epithelium” (Zhong et al., 2020) [1], we reported ophthalmoscopic observations of focal autofluorescent lesions or puncta in the Cln3Δex7/8 mouse retina at as young as 8 month old. In this data article, we performed differential interference contrast and confocal imaging analyses in all retinal layers to localize and characterize these autofluorescent lesions, including their spectral characteristics and morphology. We further studied colocalization of these autofluorescent lesions with the JNCL marker mitochondrial ATP synthase F0 sub-complex subunit C and various established retinal cell type markers.

Document Type

Article

Publication Date

10-2020

Notes/Citation Information

Published in Data in Brief, v. 32, 106076.

© 2020 The Author(s)

This is an open access article under the CC BY-NC-ND license. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

Digital Object Identifier (DOI)

https://doi.org/10.1016/j.dib.2020.106076

Funding Information

This work was supported by National Institutes of Health Center of Biomedical Research Excellence (COBRE) award P20GM121327 (pilot grant to Q.J.W.), and National Institutes of Health EY028206 and BrightFocus Foundation (to M.E.K.).

Related Content

Supplementary material associated with this article can be found in the online version at doi:10.1016/j.dib.2020.106076. It is also available for download as the additional file listed at the end of this record.

This article refers to:

Zhong, Y., Mohan, K., Liu, J., Al-Attar, A., Lin, P., Flight, R. M., Sun, Q., Warmoes, M. O., Deshpande, R. R., Liu, H., Jung, K. S., Mitov, M. I., Lin, N., Butterfield, D. A., Lu, S., Liu, J., Moseley, H. N. B., Fan, T. W. M., Kleinman, M. E., & Wang, Q. J. (2020). Loss of CLN3, the gene mutated in juvenile neuronal ceroid lipofuscinosis, leads to metabolic impairment and autophagy induction in retinal pigment epithelium. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1866(10), 165883. https://doi.org/10.1016/j.bbadis.2020.165883

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