Evidence map›Paper›PMID 27226480›Full record

ArticleMolecular biology of the cell2016

Iterative sorting of apical and basolateral cargo in Madin-Darby canine kidney cells.

Aleksandr Treyer, Mario Pujato, Ximo Pechuan, Anne Müsch

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Antioxidant Potential ofAdvances in pharmacological and pharmaceutical sciences · 2025
    Article
  4. Impact of nanoparticles on human health and disease.Nepal journal of epidemiology · 2023
    Article
  5. Article
  6. Live-cell Imaging of Biosynthetic Protein Transport in Hepatocytes.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  7. Article
  8. Toxicity of Microplastics and Nanoplastics in Mammalian Systems.International journal of environmental research and public health · 2020
    Review
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

4 authors.

Aleksandr TreyerDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Mario PujatoDepartment of Systems and Computational Biology, Albert Einstein College of Medicine, Bronx, NY 10461 Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229.
Ximo PechuanDepartment of Systems and Computational Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Anne MüschDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461 anne.muesch@einstein.yu.edu.

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI Ulrich Steidl · 1985 to 2026
$111.2M
Special Animal CoreP30DK041296 · NIDDK · YESHIVA UNIVERSITY · PI GUPTA, SANJEEV · 1989 to 2018
$22.9M
Mechanisms of luminal protein targeting in kidney and hepatic epithelial cellsR01DK064842 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI MUESCH, ANNE · 2005 to 2015
$4.1M
NCI NIH HHS P30 CA013330NIDDK NIH HHS P30 DK041296NIDDK NIH HHS R01 DK064842
6 · The paper itself

Abstract

For several decades, the trans-Golgi network (TGN) was considered the most distal stop and hence the ultimate protein-sorting station for distinct apical and basolateral transport carriers that reach their respective surface domains in the direct trafficking pathway. However, recent reports of apical and basolateral cargoes traversing post-Golgi compartments accessible to endocytic ligands before their arrival at the cell surface and the post-TGN breakup of large pleomorphic membrane fragments that exit the Golgi region toward the surface raised the possibility that compartments distal to the TGN mediate or contribute to biosynthetic sorting. Here we describe the development of a novel assay that quantitatively distinguishes different cargo pairs by their degree of colocalization at the TGN and by the evolution of colocalization during their TGN-to-surface transport. Keys to the high resolution of our approach are 1) conversion of perinuclear organelle clustering into a two-dimensional microsomal spread and 2) identification of TGN and post-TGN cargo without the need for a TGN marker that universally cosegregates with all cargo. Using our assay, we provide the first evidence that apical NTRp75 and basolateral VSVG in Madin-Darby canine kidney cells still undergo progressive sorting after they exit the TGN toward the cell surface.

Indexed as

AnimalsCell LineCell MembraneCell MovementCell PolarityDogsGolgi ApparatusKidneyMadin Darby Canine Kidney CellsMembrane GlycoproteinsMembrane ProteinsProtein TransportReceptor, Nerve Growth Factortrans-Golgi NetworkViral Envelope ProteinsG protein, vesicular stomatitis virusMembrane GlycoproteinsMembrane ProteinsReceptor, Nerve Growth FactorViral Envelope Proteins

Identifiers

PMID27226480
PMCPMC4945143

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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 Socratic graph.