Evidence map›Paper›PMID 35320536›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

Transcytosis of Galectin-3 in Mouse Intestine.

Alena Ivashenka, Christian Wunder, Valerie Chambon, Estelle Dransart, Ludger Johannes, Massiullah Shafaq-Zadah

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Spatial N-glycan rearrangement on αNature communications · 2025
    Article
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 1 country.

Alena IvashenkaCellular and Chemical Biology Unit, Endocytic Trafficking and Intracellular Delivery Team, U1143 INSERM, UMR3666 CNRS, Institut Curie, PSL Research University, Paris Cedex, France.
Christian WunderCellular and Chemical Biology Unit, Endocytic Trafficking and Intracellular Delivery Team, U1143 INSERM, UMR3666 CNRS, Institut Curie, PSL Research University, Paris Cedex, France.
Valerie ChambonCellular and Chemical Biology Unit, Endocytic Trafficking and Intracellular Delivery Team, U1143 INSERM, UMR3666 CNRS, Institut Curie, PSL Research University, Paris Cedex, France.
Estelle DransartCellular and Chemical Biology Unit, Endocytic Trafficking and Intracellular Delivery Team, U1143 INSERM, UMR3666 CNRS, Institut Curie, PSL Research University, Paris Cedex, France.
Ludger JohannesCellular and Chemical Biology Unit, Endocytic Trafficking and Intracellular Delivery Team, U1143 INSERM, UMR3666 CNRS, Institut Curie, PSL Research University, Paris Cedex, France. ludger.johannes@curie.fr.
Massiullah Shafaq-ZadahCellular and Chemical Biology Unit, Endocytic Trafficking and Intracellular Delivery Team, U1143 INSERM, UMR3666 CNRS, Institut Curie, PSL Research University, Paris Cedex, France. massiullah.shafaq-zadah@curie.fr.
Centre National de la Recherche Scientifique · FRInserm · FRUniversité Paris Sciences et Lettres · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The GlycoLipid-Lectin (GL-Lect) hypothesis provides a conceptual framework to explain how endocytic pits are built in processes of clathrin-independent endocytosis. According to this hypothesis, oligomeric cellular or pathogenic lectins interact with glycosylated plasma membrane lipids in a way such as to drive the formation of tubular endocytic pits that then detach to generate clathrin-independent endocytic carriers for the cellular uptake of cellular or pathogenic products. This process operates in a complementary manner to the conventional clathrin pathway for biological function linked to cell polarity. Up to date, the premises of the GL-Lect hypothesis have been based on model membrane and cell culture experiments. It has therefore become urgent to extend its exploration to complex organisms. In the current protocol, we describe methods to study the endocytosis and transcytosis of a key driver of the GL-Lect mechanism, the cellular galectin-3, and of one of its cargoes, lactotransferrin, in enterocytes of the intact jejunum of mice. In a step-by-step manner, we present the generation of fluorescent endocytic ligands, tissue preparation for cellular uptake measurements, binding and internalization assays, tissue fixation and preparation for sectioning, light and electron microscopical observations, and quantification of data by image processing. Pitfalls are discussed to optimize the chances of success with the described methods.

Indexed as

Galectin 3JejunumTranscytosisAnimalsClathrinEndocytosisMiceClathrinGalectin 3EnterocytesGalectin-3IntestineLactotransferrinMucusTranscytosis

Identifiers

PMID35320536
OpenAlexW4220983216

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.