Evidence map›Paper›PMID 29046391›Full record

ArticleThe Biochemical journal2017

GPI-anchored proteins are confined in subdiffraction clusters at the apical surface of polarized epithelial cells.

Simona Paladino, Stéphanie Lebreton, Mickaël Lelek, Patrizia Riccio, Sergio De Nicola, Christophe Zimmer, Chiara Zurzolo

Open access · hybridAbstract read
In one paragraph

Article in The Biochemical journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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  4. 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

7 authors at 5 institutions in 2 countries.

Simona PaladinoDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Naples, Italy.
Stéphanie LebretonUnité de Trafic Membranaire et Pathogénèse, Institut Pasteur, Paris, France.
Mickaël LelekUnité Imagerie et Modélisation, Institut Pasteur, UMR 3691 CNRS, C3BI USR 3756 IP CNRS, Paris, France.
Patrizia RiccioDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Naples, Italy.
Sergio De NicolaCNR-SPIN Institute, National Research Council, Naples, Italy.
Christophe ZimmerUnité Imagerie et Modélisation, Institut Pasteur, UMR 3691 CNRS, C3BI USR 3756 IP CNRS, Paris, France.
Chiara ZurzoloUnité de Trafic Membranaire et Pathogénèse, Institut Pasteur, Paris, France zurzolo@pasteur.fr.
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FRCeinge Biotecnologie Avanzate (Italy) · ITSuperconducting and other Innovative Materials and Devices Institute · ITUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spatio-temporal compartmentalization of membrane proteins is critical for the regulation of diverse vital functions in eukaryotic cells. It was previously shown that, at the apical surface of polarized MDCK cells, glycosylphosphatidylinositol (GPI)-anchored proteins (GPI-APs) are organized in small cholesterol-independent clusters of single GPI-AP species (homoclusters), which are required for the formation of larger cholesterol-dependent clusters formed by multiple GPI-AP species (heteroclusters). This clustered organization is crucial for the biological activities of GPI-APs; hence, understanding the spatio-temporal properties of their membrane organization is of fundamental importance. Here, by using direct stochastic optical reconstruction microscopy coupled to pair correlation analysis (pc-STORM), we were able to visualize and measure the size of these clusters. Specifically, we show that they are non-randomly distributed and have an average size of 67 nm. We also demonstrated that polarized MDCK and non-polarized CHO cells have similar cluster distribution and size, but different sensitivity to cholesterol depletion. Finally, we derived a model that allowed a quantitative characterization of the cluster organization of GPI-APs at the apical surface of polarized MDCK cells for the first time. Experimental FRET (fluorescence resonance energy transfer)/FLIM (fluorescence-lifetime imaging microscopy) data were correlated to the theoretical predictions of the model.

Indexed as

Models, BiologicalAnimalsCell Membrane StructuresCell PolarityCHO CellsCricetinaeCricetulusDogsEpithelial CellsGPI-Linked ProteinsMadin Darby Canine Kidney CellsGPI-Linked ProteinsdSTORMFLIM/FRETGPI-anchored proteinsGPI-AP cluster modellingplasma membrane organizationpolarized epithelial cellssuper-resolution microscopy

Identifiers

PMID29046391
PMCPMC5712066
OpenAlexW2765179709

What Socratic holds

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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 Socratic graph.