Evidence map›Paper›PMID 33053147›Full record

ArticleThe Journal of cell biology2020

High-speed single-molecule imaging reveals signal transduction by induced transbilayer raft phases.

Ikuko Koyama-Honda, Takahiro K Fujiwara, Rinshi S Kasai, Kenichi G N Suzuki, Eriko Kajikawa, Hisae Tsuboi, Taka A Tsunoyama, Akihiro Kusumi

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 59 citations in OpenAlex.

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  10. Sorting of complex sphingolipids within the cellular endomembrane systems.Frontiers in cell and developmental biology · 2024
    Review
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  18. The plasma membrane as an adaptable fluid mosaic.Biochimica et biophysica acta. Biomembranes · 2023
    Review
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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

8 authors at 4 institutions in 1 country.

Ikuko Koyama-HondaDepartment of Biochemistry and Molecular Biology, Graduate School and Faculty of Medicine, University of Tokyo, Tokyo, Japan.
Takahiro K FujiwaraInstitute for Integrated Cell-Material Sciences, Kyoto University, Kyoto, Japan.
Rinshi S KasaiInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Kenichi G N SuzukiInstitute for Integrated Cell-Material Sciences, Kyoto University, Kyoto, Japan.
Eriko KajikawaLaboratory for Organismal Patterning, Center for Biosystems Dynamics Research, RIKEN Kobe, Kobe, Japan.
Hisae TsuboiMembrane Cooperativity Unit, Okinawa Institute of Science and Technology Graduate University, Onna-son, Okinawa, Japan.
Taka A TsunoyamaMembrane Cooperativity Unit, Okinawa Institute of Science and Technology Graduate University, Onna-son, Okinawa, Japan.
Akihiro KusumiMembrane Cooperativity Unit, Okinawa Institute of Science and Technology Graduate University, Onna-son, Okinawa, Japan.
Kyoto University · JPOkinawa Institute of Science and Technology Graduate University · JPRIKEN Center for Biosystems Dynamics Research · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using single-molecule imaging with enhanced time resolutions down to 5 ms, we found that CD59 cluster rafts and GM1 cluster rafts were stably induced in the outer leaflet of the plasma membrane (PM), which triggered the activation of Lyn, H-Ras, and ERK and continually recruited Lyn and H-Ras right beneath them in the inner leaflet with dwell lifetimes <0.1 s. The detection was possible due to the enhanced time resolutions employed here. The recruitment depended on the PM cholesterol and saturated alkyl chains of Lyn and H-Ras, whereas it was blocked by the nonraftophilic transmembrane protein moiety and unsaturated alkyl chains linked to the inner-leaflet molecules. Because GM1 cluster rafts recruited Lyn and H-Ras as efficiently as CD59 cluster rafts, and because the protein moieties of Lyn and H-Ras were not required for the recruitment, we conclude that the transbilayer raft phases induced by the outer-leaflet stabilized rafts recruit lipid-anchored signaling molecules by lateral raft-lipid interactions and thus serve as a key signal transduction platform.

Indexed as

Single Molecule ImagingCD59 AntigensG(M1) GangliosideHeLa CellsHumansMembrane MicrodomainsProto-Oncogene Proteins p21(ras)src-Family KinasesCD59 AntigensCD59 protein, humanG(M1) GangliosideHRAS protein, humanlyn protein-tyrosine kinaseProto-Oncogene Proteins p21(ras)src-Family Kinases

Identifiers

PMID33053147
PMCPMC7563750
OpenAlexW3092662338

What OpenQuestion holds

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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.