Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome.

Ciliopathies lead to multiorgan pathologies that include renal cysts, deafness, obesity and retinal degeneration. Retinal photoreceptors have connecting cilia joining the inner and outer segment that are responsible for transport of molecules to develop and maintain the outer segment process. The pr...

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Main Authors: Sarika Tiwari, Scott Hudson, Vincent H Gattone, Caroline Miller, Ellen A G Chernoff, Teri L Belecky-Adams
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23516626/pdf/?tool=EBI
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spelling doaj-a17b55a7275e4518b9b114d376fc4e302021-03-04T12:14:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5930610.1371/journal.pone.0059306Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome.Sarika TiwariScott HudsonVincent H GattoneCaroline MillerEllen A G ChernoffTeri L Belecky-AdamsCiliopathies lead to multiorgan pathologies that include renal cysts, deafness, obesity and retinal degeneration. Retinal photoreceptors have connecting cilia joining the inner and outer segment that are responsible for transport of molecules to develop and maintain the outer segment process. The present study evaluated meckelin (MKS3) expression during outer segment genesis and determined the consequences of mutant meckelin on photoreceptor development and survival in Wistar polycystic kidney disease Wpk/Wpk rat using immunohistochemistry, analysis of cell death and electron microscopy. MKS3 was ubiquitously expressed throughout the retina at postnatal day 10 (P10) and P21. However, in the mature retina, MKS3 expression was restricted to photoreceptors and the retinal ganglion cell layer. At P10, both the wild type and homozygous Wpk mutant retina had all retinal cell types. In contrast, by P21, cells expressing rod- and cone-specific markers were fewer in number and expression of opsins appeared to be abnormally localized to the cell body. Cell death analyses were consistent with the disappearance of photoreceptor-specific markers and showed that the cells were undergoing caspase-dependent cell death. By electron microscopy, P10 photoreceptors showed rudimentary outer segments with an axoneme, but did not develop outer segment discs that were clearly present in the wild type counterpart. At p21 the mutant outer segments appeared much the same as the P10 mutant outer segments with only a short axoneme, while the wild-type controls had developed outer segments with many well-organized discs. We conclude that MKS3 is not important for formation of connecting cilium and rudimentary outer segments, but is critical for the maturation of outer segment processes.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23516626/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Sarika Tiwari
Scott Hudson
Vincent H Gattone
Caroline Miller
Ellen A G Chernoff
Teri L Belecky-Adams
spellingShingle Sarika Tiwari
Scott Hudson
Vincent H Gattone
Caroline Miller
Ellen A G Chernoff
Teri L Belecky-Adams
Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome.
PLoS ONE
author_facet Sarika Tiwari
Scott Hudson
Vincent H Gattone
Caroline Miller
Ellen A G Chernoff
Teri L Belecky-Adams
author_sort Sarika Tiwari
title Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome.
title_short Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome.
title_full Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome.
title_fullStr Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome.
title_full_unstemmed Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome.
title_sort meckelin 3 is necessary for photoreceptor outer segment development in rat meckel syndrome.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Ciliopathies lead to multiorgan pathologies that include renal cysts, deafness, obesity and retinal degeneration. Retinal photoreceptors have connecting cilia joining the inner and outer segment that are responsible for transport of molecules to develop and maintain the outer segment process. The present study evaluated meckelin (MKS3) expression during outer segment genesis and determined the consequences of mutant meckelin on photoreceptor development and survival in Wistar polycystic kidney disease Wpk/Wpk rat using immunohistochemistry, analysis of cell death and electron microscopy. MKS3 was ubiquitously expressed throughout the retina at postnatal day 10 (P10) and P21. However, in the mature retina, MKS3 expression was restricted to photoreceptors and the retinal ganglion cell layer. At P10, both the wild type and homozygous Wpk mutant retina had all retinal cell types. In contrast, by P21, cells expressing rod- and cone-specific markers were fewer in number and expression of opsins appeared to be abnormally localized to the cell body. Cell death analyses were consistent with the disappearance of photoreceptor-specific markers and showed that the cells were undergoing caspase-dependent cell death. By electron microscopy, P10 photoreceptors showed rudimentary outer segments with an axoneme, but did not develop outer segment discs that were clearly present in the wild type counterpart. At p21 the mutant outer segments appeared much the same as the P10 mutant outer segments with only a short axoneme, while the wild-type controls had developed outer segments with many well-organized discs. We conclude that MKS3 is not important for formation of connecting cilium and rudimentary outer segments, but is critical for the maturation of outer segment processes.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23516626/pdf/?tool=EBI
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