Evidence map›Paper›PMID 30967612›Full record

ArticleScientific reports2019

Formation of tubules and helical ribbons by ceramide phosphoethanolamine-containing membranes.

Takehiko Inaba, Motohide Murate, Nario Tomishige, Yan-Fen Lee, Françoise Hullin-Matsuda, Brigitte Pollet, Nicolas Humbert, Yves Mély, Yasushi Sako, Peter Greimel and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

6 citing papers in PubMed, 67 citations in OpenAlex.

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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

11 authors at 7 institutions in 3 countries.

Takehiko InabaLipid Biology Laboratory, RIKEN, 2-1, Hirosawa, Wako, Saitama, 351-0198, Japan.
Motohide MurateLipid Biology Laboratory, RIKEN, 2-1, Hirosawa, Wako, Saitama, 351-0198, Japan.
Nario TomishigeLipid Biology Laboratory, RIKEN, 2-1, Hirosawa, Wako, Saitama, 351-0198, Japan.
Yan-Fen LeeLipid Biology Laboratory, RIKEN, 2-1, Hirosawa, Wako, Saitama, 351-0198, Japan.
Françoise Hullin-MatsudaLipid Biology Laboratory, RIKEN, 2-1, Hirosawa, Wako, Saitama, 351-0198, Japan.
Brigitte PolletLaboratoire de Bioimagerie et Pathologies, UMR 7021 CNRS, Université de Strasbourg, Faculté de Pharmacie, 74 route du Rhin, 67401, Illkirch, France.
Nicolas HumbertLaboratoire de Bioimagerie et Pathologies, UMR 7021 CNRS, Université de Strasbourg, Faculté de Pharmacie, 74 route du Rhin, 67401, Illkirch, France.
Yves MélyLaboratoire de Bioimagerie et Pathologies, UMR 7021 CNRS, Université de Strasbourg, Faculté de Pharmacie, 74 route du Rhin, 67401, Illkirch, France.ORCID http://orcid.org/0000-0001-7328-8269
Yasushi SakoCellular Informatics Laboratory, RIKEN, 2-1, Hirosawa, Wako, Saitama, 351-0198, Japan.
Peter GreimelLipid Biology Laboratory, RIKEN, 2-1, Hirosawa, Wako, Saitama, 351-0198, Japan.
Toshihide KobayashiLipid Biology Laboratory, RIKEN, 2-1, Hirosawa, Wako, Saitama, 351-0198, Japan. toshihide.kobayashi@unistra.fr.
Centre National de la Recherche Scientifique · FRObayashi (Japan) · JPRCSI & UCD Malaysia Campus · MYRIKEN · JPRIKEN Advanced Science Institute · JPRIKEN Center for Brain Science · JPUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ceramide phosphoethanolamine (CPE), a major sphingolipid in invertebrates, is crucial for axonal ensheathment in Drosophila. Darkfield microscopy revealed that an equimolar mixture of bovine buttermilk CPE (milk CPE) and 1,2-dioleoyl-sn-glycero-3-phosphocholine (diC18:1 PC) tends to form tubules and helical ribbons, while pure milk CPE mainly exhibits amorphous aggregates and, at low frequency, straight needles. Negative staining electron microscopy indicated that helices and tubules were composed of multilayered 5-10 nm thick slab-like structures. Using different molecular species of PC and CPE, we demonstrated that the acyl chain length of CPE but not of PC is crucial for the formation of tubules and helices in equimolar mixtures. Incubation of the lipid suspensions at the respective phase transition temperature of CPE facilitated the formation of both tubules and helices, suggesting a dynamic lipid rearrangement during formation. Substituting diC18:1 PC with diC18:1 PE or diC18:1 PS failed to form tubules and helices. As hydrated galactosylceramide (GalCer), a major lipid in mammalian myelin, has been reported to spontaneously form tubules and helices, it is believed that the ensheathment of axons in mammals and Drosophila is based on similar physical processes with different lipids.

Indexed as

AnimalsAxon FasciculationDrosophilaGalactosylceramidesLipid BilayersMembranesMolecular ConformationNervous SystemPhase TransitionPhosphatidylcholinesSphingomyelins1,2-oleoylphosphatidylcholineceramide phosphoethanolamineGalactosylceramidesLipid BilayersPhosphatidylcholinesSphingomyelins

Identifiers

PMID30967612
PMCPMC6456502
OpenAlexW2936489451

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.