Evidence map›Paper›PMID 26272915›Full record

ArticleJournal of cell science2015

Induction of lateral lumens through disruption of a monoleucine-based basolateral-sorting motif in betacellulin.

Bhuminder Singh, Galina Bogatcheva, Alina Starchenko, Justine Sinnaeve, Lynne A Lapierre, Janice A Williams, James R Goldenring, Robert J Coffey

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Cell-Cell Contact and Receptor Tyrosine Kinase Signaling.Cold Spring Harbor perspectives in biology · 2018
    Review
  10. 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

8 authors at 1 institution in 1 country.

Bhuminder SinghDepartment of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Epithelial Biology Center, Vanderbilt University School of Medicine, Nashville, TN 37232, USA bhuminder.singh@vanderbilt.edu.
Galina BogatchevaDepartment of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Epithelial Biology Center, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Alina StarchenkoDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Justine SinnaeveInterdisciplinary Graduate Program, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Lynne A LapierreEpithelial Biology Center, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Department of Surgery, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Janice A WilliamsVanderbilt Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Cell Imaging Shared Resource, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
James R GoldenringDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Epithelial Biology Center, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Department of Surgery, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Department of Veteran Affairs Medical Center, Nashville, TN 37232, USA.
Robert J CoffeyDepartment of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Epithelial Biology Center, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Department of Veteran Affairs Medical Center, Nashville, TN 37232, USA.
Vanderbilt University · US

Funding

Understanding and Controlling p120 Dysfunction in CRCP50CA095103 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI COFFEY, ROBERT J. · 2002 to 2017
$33.6M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
SMALL GTP BINDING PROTEINS IN GASTROINTESTINAL MUCOSAR01DK048370 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GOLDENRING, JAMES RICHARD · 1994 to 2025
$10.1M
TRANSFORMING GROWTH FACTORS IN COLONIC NEOPLASIAR01CA046413 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI COFFEY, ROBERT J. · 1988 to 2016
$8.8M
BIOCHEMICAL &CHEMICAL TRAINING FOR CANCER RESEARCHT32CA009582 · NCI · VANDERBILT UNIVERSITY · PI David K Cortez · 1987 to 2026
$8.8M
Integrated Biological Systems Training in OncologyT32CA119925 · NCI · VANDERBILT UNIVERSITY · PI Vivian Gama, William Patrick Tansey · 2008 to 2026
$7.6M
Molecular characteristics of the apical recycling systemR01DK070856 · NIDDK · VANDERBILT UNIVERSITY · PI GOLDENRING, JAMES RICHARD · 2006 to 2014
$3.1M
PET System for Preclinical ResearchS10OD016245 · OD · VANDERBILT UNIVERSITY · PI PETERSON, TODD E · 2013 to 2013
$584k
NCI NIH HHS P50 CA095103NCI NIH HHS P50-CA95103NCI NIH HHS R01 CA046413NCI NIH HHS R01-CA46413NCI NIH HHS T32 CA009582NCI NIH HHS T32 CA119925NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK048370NIDDK NIH HHS R01 DK070856NIDDK NIH HHS R01-DK48370NIDDK NIH HHS R01-DK70856NIH HHS S10 OD016245
6 · The paper itself

Abstract

Directed delivery of EGF receptor (EGFR) ligands to the apical or basolateral surface is a crucial regulatory step in the initiation of EGFR signaling in polarized epithelial cells. Herein, we show that the EGFR ligand betacellulin (BTC) is preferentially sorted to the basolateral surface of polarized MDCK cells. By using sequential truncations and site-directed mutagenesis within the BTC cytoplasmic domain, combined with selective cell-surface biotinylation and immunofluorescence, we have uncovered a monoleucine-based basolateral-sorting motif (EExxxL, specifically (156)EEMETL(161)). Disruption of this sorting motif led to equivalent apical and basolateral localization of BTC. Unlike other EGFR ligands, BTC mistrafficking induced formation of lateral lumens in polarized MDCK cells, and this process was significantly attenuated by inhibition of EGFR. Additionally, expression of a cancer-associated somatic BTC mutation (E156K) led to BTC mistrafficking and induced lateral lumens in MDCK cells. Overexpression of BTC, especially mistrafficking forms, increased the growth of MDCK cells. These results uncover a unique role for BTC mistrafficking in promoting epithelial reorganization.

Indexed as

BetacellulinCell PolarityAmino Acid SequenceAnimalsDogsEGF Family of ProteinsErbB ReceptorsFluorescent Antibody TechniqueMadin Darby Canine Kidney CellsMutationProtein Sorting SignalsProtein Structure, TertiaryBetacellulinEGF Family of ProteinsErbB ReceptorsProtein Sorting SignalsBetacellulinEGFR signalingEpithelial polarityLateral lumensMDCK cellsPolarized trafficking

Identifiers

PMID26272915
PMCPMC4582402
OpenAlexW2096470960

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.