Lack of Acid Sphingomyelinase Induces Age-Related Retinal Degeneration.

Mutations of acid sphingomyelinase (ASMase) cause Niemann-Pick diseases type A and B, which are fatal inherited lipid lysosomal storage diseases, characterized with visceral organ abnormalities and neurodegeneration. However, the effects of suppressing retinal ASMase expression are not understood. T...

Full description

Bibliographic Details
Main Authors: Bill X Wu, Jie Fan, Nicholas P Boyer, Russell W Jenkins, Yiannis Koutalos, Yusuf A Hannun, Craig E Crosson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4500403?pdf=render
_version_ 1818287307070898176
author Bill X Wu
Jie Fan
Nicholas P Boyer
Russell W Jenkins
Yiannis Koutalos
Yusuf A Hannun
Craig E Crosson
author_facet Bill X Wu
Jie Fan
Nicholas P Boyer
Russell W Jenkins
Yiannis Koutalos
Yusuf A Hannun
Craig E Crosson
author_sort Bill X Wu
collection DOAJ
description Mutations of acid sphingomyelinase (ASMase) cause Niemann-Pick diseases type A and B, which are fatal inherited lipid lysosomal storage diseases, characterized with visceral organ abnormalities and neurodegeneration. However, the effects of suppressing retinal ASMase expression are not understood. The goal of this study was to determine if the disruption of ASMase expression impacts the retinal structure and function in the mouse, and begin to investigate the mechanisms underlying these abnormalities.Acid sphingomyelinase knockout (ASMase KO) mice were utilized to study the roles of this sphingolipid metabolizing enzyme in the retina. Electroretinogram and morphometric analysis were used to assess the retinal function and structure at various ages. Sphingolipid profile was determined by liquid chromatography-mass spectrometry. Western blots evaluated the level of the autophagy marker LC3-II.When compared to control animals, ASMase KO mice exhibited significant age-dependent reduction in ERG a- and b-wave amplitudes. Associated with these functional deficits, morphometric analysis revealed progressive thinning of retinal layers; however, the most prominent degeneration was observed in the photoreceptor and outer nuclear layer. Additional analyses of ASMase KO mice revealed early reduction in ERG c-wave amplitudes and increased lipofuscin accumulation in the retinal pigment epithelium (RPE). Sphingolipid analyses showed abnormal accumulation of sphingomyelin and sphingosine in ASMase KO retinas. Western blot analyses showed a higher level of the autophagosome marker LC3-II.These studies demonstrate that ASMase is necessary for the maintenance of normal retinal structure and function. The early outer retinal dysfunction, outer segment degeneration, accumulation of lipofuscin and autophagosome markers provide evidence that disruption of lysosomal function contributes to the age-dependent retinal degeneration exhibited by ASMase KO mice.
first_indexed 2024-12-13T01:38:24Z
format Article
id doaj.art-c4368c7f3dce44b19e1a665ea1fb1f6b
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-13T01:38:24Z
publishDate 2015-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-c4368c7f3dce44b19e1a665ea1fb1f6b2022-12-22T00:03:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01107e013303210.1371/journal.pone.0133032Lack of Acid Sphingomyelinase Induces Age-Related Retinal Degeneration.Bill X WuJie FanNicholas P BoyerRussell W JenkinsYiannis KoutalosYusuf A HannunCraig E CrossonMutations of acid sphingomyelinase (ASMase) cause Niemann-Pick diseases type A and B, which are fatal inherited lipid lysosomal storage diseases, characterized with visceral organ abnormalities and neurodegeneration. However, the effects of suppressing retinal ASMase expression are not understood. The goal of this study was to determine if the disruption of ASMase expression impacts the retinal structure and function in the mouse, and begin to investigate the mechanisms underlying these abnormalities.Acid sphingomyelinase knockout (ASMase KO) mice were utilized to study the roles of this sphingolipid metabolizing enzyme in the retina. Electroretinogram and morphometric analysis were used to assess the retinal function and structure at various ages. Sphingolipid profile was determined by liquid chromatography-mass spectrometry. Western blots evaluated the level of the autophagy marker LC3-II.When compared to control animals, ASMase KO mice exhibited significant age-dependent reduction in ERG a- and b-wave amplitudes. Associated with these functional deficits, morphometric analysis revealed progressive thinning of retinal layers; however, the most prominent degeneration was observed in the photoreceptor and outer nuclear layer. Additional analyses of ASMase KO mice revealed early reduction in ERG c-wave amplitudes and increased lipofuscin accumulation in the retinal pigment epithelium (RPE). Sphingolipid analyses showed abnormal accumulation of sphingomyelin and sphingosine in ASMase KO retinas. Western blot analyses showed a higher level of the autophagosome marker LC3-II.These studies demonstrate that ASMase is necessary for the maintenance of normal retinal structure and function. The early outer retinal dysfunction, outer segment degeneration, accumulation of lipofuscin and autophagosome markers provide evidence that disruption of lysosomal function contributes to the age-dependent retinal degeneration exhibited by ASMase KO mice.http://europepmc.org/articles/PMC4500403?pdf=render
spellingShingle Bill X Wu
Jie Fan
Nicholas P Boyer
Russell W Jenkins
Yiannis Koutalos
Yusuf A Hannun
Craig E Crosson
Lack of Acid Sphingomyelinase Induces Age-Related Retinal Degeneration.
PLoS ONE
title Lack of Acid Sphingomyelinase Induces Age-Related Retinal Degeneration.
title_full Lack of Acid Sphingomyelinase Induces Age-Related Retinal Degeneration.
title_fullStr Lack of Acid Sphingomyelinase Induces Age-Related Retinal Degeneration.
title_full_unstemmed Lack of Acid Sphingomyelinase Induces Age-Related Retinal Degeneration.
title_short Lack of Acid Sphingomyelinase Induces Age-Related Retinal Degeneration.
title_sort lack of acid sphingomyelinase induces age related retinal degeneration
url http://europepmc.org/articles/PMC4500403?pdf=render
work_keys_str_mv AT billxwu lackofacidsphingomyelinaseinducesagerelatedretinaldegeneration
AT jiefan lackofacidsphingomyelinaseinducesagerelatedretinaldegeneration
AT nicholaspboyer lackofacidsphingomyelinaseinducesagerelatedretinaldegeneration
AT russellwjenkins lackofacidsphingomyelinaseinducesagerelatedretinaldegeneration
AT yianniskoutalos lackofacidsphingomyelinaseinducesagerelatedretinaldegeneration
AT yusufahannun lackofacidsphingomyelinaseinducesagerelatedretinaldegeneration
AT craigecrosson lackofacidsphingomyelinaseinducesagerelatedretinaldegeneration