Cargando…

The WAVE complex drives the morphogenesis of the photoreceptor outer segment cilium

The photoreceptor outer segment is a modified cilium filled with hundreds of flattened “disc” membranes responsible for efficient light capture. To maintain photoreceptor health and functionality, outer segments are continuously renewed through the addition of new discs at their base. This process i...

Descripción completa

Detalles Bibliográficos
Autores principales: Spencer, William J., Schneider, Nicholas F., Lewis, Tylor R., Castillo, Carson M., Skiba, Nikolai P., Arshavsky, Vadim Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041111/
https://www.ncbi.nlm.nih.gov/pubmed/36917665
http://dx.doi.org/10.1073/pnas.2215011120
_version_ 1784912635316142080
author Spencer, William J.
Schneider, Nicholas F.
Lewis, Tylor R.
Castillo, Carson M.
Skiba, Nikolai P.
Arshavsky, Vadim Y.
author_facet Spencer, William J.
Schneider, Nicholas F.
Lewis, Tylor R.
Castillo, Carson M.
Skiba, Nikolai P.
Arshavsky, Vadim Y.
author_sort Spencer, William J.
collection PubMed
description The photoreceptor outer segment is a modified cilium filled with hundreds of flattened “disc” membranes responsible for efficient light capture. To maintain photoreceptor health and functionality, outer segments are continuously renewed through the addition of new discs at their base. This process is driven by branched actin polymerization nucleated by the Arp2/3 complex. To induce actin polymerization, Arp2/3 requires a nucleation promoting factor. Here, we show that the nucleation promoting factor driving disc morphogenesis is the pentameric WAVE complex and identify all protein subunits of this complex. We further demonstrate that the knockout of one of them, WASF3, abolishes actin polymerization at the site of disc morphogenesis leading to formation of disorganized membrane lamellae emanating from the photoreceptor cilium instead of an outer segment. These data establish that, despite the intrinsic ability of photoreceptor ciliary membranes to form lamellar structures, WAVE-dependent actin polymerization is essential for organizing these membranes into a proper outer segment.
format Online
Article
Text
id pubmed-10041111
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-100411112023-09-14 The WAVE complex drives the morphogenesis of the photoreceptor outer segment cilium Spencer, William J. Schneider, Nicholas F. Lewis, Tylor R. Castillo, Carson M. Skiba, Nikolai P. Arshavsky, Vadim Y. Proc Natl Acad Sci U S A Biological Sciences The photoreceptor outer segment is a modified cilium filled with hundreds of flattened “disc” membranes responsible for efficient light capture. To maintain photoreceptor health and functionality, outer segments are continuously renewed through the addition of new discs at their base. This process is driven by branched actin polymerization nucleated by the Arp2/3 complex. To induce actin polymerization, Arp2/3 requires a nucleation promoting factor. Here, we show that the nucleation promoting factor driving disc morphogenesis is the pentameric WAVE complex and identify all protein subunits of this complex. We further demonstrate that the knockout of one of them, WASF3, abolishes actin polymerization at the site of disc morphogenesis leading to formation of disorganized membrane lamellae emanating from the photoreceptor cilium instead of an outer segment. These data establish that, despite the intrinsic ability of photoreceptor ciliary membranes to form lamellar structures, WAVE-dependent actin polymerization is essential for organizing these membranes into a proper outer segment. National Academy of Sciences 2023-03-14 2023-03-21 /pmc/articles/PMC10041111/ /pubmed/36917665 http://dx.doi.org/10.1073/pnas.2215011120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Spencer, William J.
Schneider, Nicholas F.
Lewis, Tylor R.
Castillo, Carson M.
Skiba, Nikolai P.
Arshavsky, Vadim Y.
The WAVE complex drives the morphogenesis of the photoreceptor outer segment cilium
title The WAVE complex drives the morphogenesis of the photoreceptor outer segment cilium
title_full The WAVE complex drives the morphogenesis of the photoreceptor outer segment cilium
title_fullStr The WAVE complex drives the morphogenesis of the photoreceptor outer segment cilium
title_full_unstemmed The WAVE complex drives the morphogenesis of the photoreceptor outer segment cilium
title_short The WAVE complex drives the morphogenesis of the photoreceptor outer segment cilium
title_sort wave complex drives the morphogenesis of the photoreceptor outer segment cilium
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041111/
https://www.ncbi.nlm.nih.gov/pubmed/36917665
http://dx.doi.org/10.1073/pnas.2215011120
work_keys_str_mv AT spencerwilliamj thewavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT schneidernicholasf thewavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT lewistylorr thewavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT castillocarsonm thewavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT skibanikolaip thewavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT arshavskyvadimy thewavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT spencerwilliamj wavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT schneidernicholasf wavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT lewistylorr wavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT castillocarsonm wavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT skibanikolaip wavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium
AT arshavskyvadimy wavecomplexdrivesthemorphogenesisofthephotoreceptoroutersegmentcilium