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Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods
BACKGROUND: Cilia are vital to various cellular and sensory functions. The pathway by which ciliary membrane proteins translocate through the transition zone is not well understood. Direct morphological characterization of ciliary cargoes in transit remains lacking. In the vertebrate photoreceptor,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320831/ https://www.ncbi.nlm.nih.gov/pubmed/25664179 http://dx.doi.org/10.1186/s13630-015-0013-1 |
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author | Chuang, Jen-Zen Hsu, Ya-Chu Sung, Ching-Hwa |
author_facet | Chuang, Jen-Zen Hsu, Ya-Chu Sung, Ching-Hwa |
author_sort | Chuang, Jen-Zen |
collection | PubMed |
description | BACKGROUND: Cilia are vital to various cellular and sensory functions. The pathway by which ciliary membrane proteins translocate through the transition zone is not well understood. Direct morphological characterization of ciliary cargoes in transit remains lacking. In the vertebrate photoreceptor, rhodopsin is synthesized and transported from the inner segment to the disc membranes of the outer segment (OS), which is a modified cilium. To date, the membrane topology of the basal OS and the mechanisms by which rhodopsin is transported through the transition zone (i.e., connecting cilium) and by which nascent disc membranes are formed remain controversial. RESULTS: Using an antibody recognizing its cytoplasmic C-terminus, we localize rhodopsin on both the plasma membrane and lumen of the connecting cilium by immuno-electron microscopy (EM). We also use transmission EM to visualize the electron-dense enzymatic products derived from the rhodopsin-horseradish peroxidase (HRP) fusion in transfected rodent rods. In the connecting cilium, rhodopsin is not only expressed in the plasma membrane but also in the lumen on two types of membranous carriers, long smooth tubules and small, coated, filament-bound vesicles. Additionally, membrane-bound rhodopsin carriers are also found in close proximity to the nascent discs at the basal OS axoneme and in the distal inner segment. This topology-indicative HRP-rhodopsin reporter shows that the nascent basalmost discs and the mature discs have the same membrane topology, with no indication of evagination or invagination from the basal OS plasma membranes. Serial block face and focus ion beam scanning EM analyses both indicate that the transport carriers enter the connecting cilium lumen from either the basal body lumen or cytoplasmic space between the axonemal microtubules and the ciliary plasma membrane. CONCLUSIONS: Our results suggest the existence of multiple ciliary gate entry pathways in rod photoreceptors. Rhodopsin is likely transported across the connecting cilium on the plasma membrane and through the lumens on two types of tubulovesicular carriers produced in the inner segment. Our findings agree with a previous model that rhodopsin carriers derived from the cell body may fuse directly onto nascent discs as they grow and mature. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13630-015-0013-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4320831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43208312015-02-09 Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods Chuang, Jen-Zen Hsu, Ya-Chu Sung, Ching-Hwa Cilia Research BACKGROUND: Cilia are vital to various cellular and sensory functions. The pathway by which ciliary membrane proteins translocate through the transition zone is not well understood. Direct morphological characterization of ciliary cargoes in transit remains lacking. In the vertebrate photoreceptor, rhodopsin is synthesized and transported from the inner segment to the disc membranes of the outer segment (OS), which is a modified cilium. To date, the membrane topology of the basal OS and the mechanisms by which rhodopsin is transported through the transition zone (i.e., connecting cilium) and by which nascent disc membranes are formed remain controversial. RESULTS: Using an antibody recognizing its cytoplasmic C-terminus, we localize rhodopsin on both the plasma membrane and lumen of the connecting cilium by immuno-electron microscopy (EM). We also use transmission EM to visualize the electron-dense enzymatic products derived from the rhodopsin-horseradish peroxidase (HRP) fusion in transfected rodent rods. In the connecting cilium, rhodopsin is not only expressed in the plasma membrane but also in the lumen on two types of membranous carriers, long smooth tubules and small, coated, filament-bound vesicles. Additionally, membrane-bound rhodopsin carriers are also found in close proximity to the nascent discs at the basal OS axoneme and in the distal inner segment. This topology-indicative HRP-rhodopsin reporter shows that the nascent basalmost discs and the mature discs have the same membrane topology, with no indication of evagination or invagination from the basal OS plasma membranes. Serial block face and focus ion beam scanning EM analyses both indicate that the transport carriers enter the connecting cilium lumen from either the basal body lumen or cytoplasmic space between the axonemal microtubules and the ciliary plasma membrane. CONCLUSIONS: Our results suggest the existence of multiple ciliary gate entry pathways in rod photoreceptors. Rhodopsin is likely transported across the connecting cilium on the plasma membrane and through the lumens on two types of tubulovesicular carriers produced in the inner segment. Our findings agree with a previous model that rhodopsin carriers derived from the cell body may fuse directly onto nascent discs as they grow and mature. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13630-015-0013-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-08 /pmc/articles/PMC4320831/ /pubmed/25664179 http://dx.doi.org/10.1186/s13630-015-0013-1 Text en © Chuang et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Chuang, Jen-Zen Hsu, Ya-Chu Sung, Ching-Hwa Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods |
title | Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods |
title_full | Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods |
title_fullStr | Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods |
title_full_unstemmed | Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods |
title_short | Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods |
title_sort | ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320831/ https://www.ncbi.nlm.nih.gov/pubmed/25664179 http://dx.doi.org/10.1186/s13630-015-0013-1 |
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