Evidence map›Paper›PMID 26668363›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Rod disc renewal occurs by evagination of the ciliary plasma membrane that makes cadherin-based contacts with the inner segment.

Thomas Burgoyne, Ingrid P Meschede, Jemima J Burden, Maryse Bailly, Miguel C Seabra, Clare E Futter

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

72 citing papers in PubMed, 133 citations in OpenAlex.

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  13. Rescue of cone and rod photoreceptor function in a CDHR1-model of age-related retinal degeneration.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
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12 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Thomas BurgoyneInstitute of Ophthalmology, University College London, London, EC1V9EL, United Kingdom;
Ingrid P MeschedeInstitute of Ophthalmology, University College London, London, EC1V9EL, United Kingdom;
Jemima J BurdenLaboratory for Molecular and Cell Biology, University College London, London, WC1E6BT, United Kingdom;ORCID http://orcid.org/0000-0001-5894-7043
Maryse BaillyInstitute of Ophthalmology, University College London, London, EC1V9EL, United Kingdom;
Miguel C SeabraNational Heart and Lung Institute, Imperial College, London, SW72AZ, United Kingdom; Centro de Estudos de Doenças Crónicas, NOVA Medical School/Faculdade de Ciências Médicas, Universidade Nova de Lisboa, 1169-056, Lisboa, Portugal.
Clare E FutterInstitute of Ophthalmology, University College London, London, EC1V9EL, United Kingdom; c.futter@ucl.ac.uk.
University College London · GBImperial College London · GBMRC Laboratory for Molecular Cell Biology · GB

Funding

Medical Research Council G0700778Wellcome Trust 093445
6 · The paper itself

Abstract

The outer segments of vertebrate rod photoreceptors are renewed every 10 d. Outer segment components are transported from the site of synthesis in the inner segment through the connecting cilium, followed by assembly of the highly ordered discs. Two models of assembly of discrete discs involving either successive fusion events between intracellular rhodopsin-bearing vesicles or the evagination of the plasma membrane followed by fusion of adjacent evaginations have been proposed. Here we use immuno-electron microscopy and electron tomography to show that rhodopsin is transported from the inner to the outer segment via the ciliary plasma membrane, subsequently forming successive evaginations that "zipper" up proximally, but at their leading edges are free to make junctions containing the protocadherin, PCDH21, with the inner segment plasma membrane. Given the physical dimensions of the evaginations, coupled with likely instability of the membrane cortex at the distal end of the connecting cilium, we propose that the evagination occurs via a process akin to blebbing and is not driven by actin polymerization. Disassembly of these junctions is accompanied by fusion of the leading edges of successive evaginations to form discrete discs. This fusion is topologically different to that mediated by the membrane fusion proteins, SNAREs, as initial fusion is between exoplasmic leaflets, and is accompanied by gain of the tetraspanin rim protein, peripherin.

Indexed as

AnimalsCadherin Related ProteinsCadherinsCell MembraneCryoelectron MicroscopyElectron Microscope TomographyEyeEye ProteinsMice, Inbred C57BLMicroscopy, ImmunoelectronMunc18 ProteinsNerve Tissue ProteinsPhotoreceptor CellsQa-SNARE ProteinsRetinal Photoreceptor Cell Inner SegmentRetinal Rod Photoreceptor CellsCadherin Related ProteinsCadherinsCDHR1 protein, humanEye ProteinsMunc18 ProteinsNerve Tissue ProteinsQa-SNARE ProteinsRhodopsindisc renewalprotocadherinrhodopsinrod photoreceptors

Identifiers

PMID26668363
PMCPMC4702997
OpenAlexW2218417668

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.