Evidence map›Paper›PMID 25833710›Full record

ArticleMolecular biology of the cell2015

The Arp2/3 complex has essential roles in vesicle trafficking and transcytosis in the mammalian small intestine.

Kang Zhou, Kaelyn D Sumigray, Terry Lechler

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

31 citing papers in PubMed, 46 citations in OpenAlex.

  1. Trial
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  9. Article
  10. Transcytosis of Galectin-3 in Mouse Intestine.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  11. Functions of Arp2/3 Complex in the Dynamics of Epithelial Tissues.Frontiers in cell and developmental biology · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Lung Endothelial Transcytosis.Comprehensive Physiology · 2020
    Review
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Kang ZhouDepartment of Dermatology and Department of Cell Biology, Duke University Medical Center, Durham, NC 27710.
Kaelyn D SumigrayDepartment of Dermatology and Department of Cell Biology, Duke University Medical Center, Durham, NC 27710.
Terry LechlerDepartment of Dermatology and Department of Cell Biology, Duke University Medical Center, Durham, NC 27710 terry.lechler@duke.edu.
Duke University · US

Funding

Role of Cell Adhesion and the Cytoskeleton in Epidermal IntegrityR01AR055926 · NIAMS · DUKE UNIVERSITY · PI LECHLER, TERRY H · 2009 to 2019
$3.7M
Differentiation Induced Changes in Centrosomes and Microtubule OrganizationR01GM111336 · NIGMS · DUKE UNIVERSITY · PI LECHLER, TERRY H · 2014 to 2017
$1.2M
NIAMS NIH HHS R01 AR055926NIAMS NIH HHS R01-AR055926NIGMS NIH HHS R01 GM111336NIGMS NIH HHS R01-GM111336
6 · The paper itself

Abstract

The Arp2/3 complex is the only known nucleator of branched F-actin filaments. Work in cultured cells has established a wide array of functions for this complex in controlling cell migration, shape, and adhesion. However, loss of Arp2/3 complex function in tissues has yielded cell type-specific phenotypes. Here we report essential functions of the Arp2/3 complex in the intestinal epithelium. The Arp2/3 complex was dispensable for intestinal development, generation of cortical F-actin, and cell polarity. However, it played essential roles in vesicle trafficking. We found that in the absence of ArpC3, enterocytes had defects in the organization of the endolysosomal system. These defects were physiologically relevant, as transcytosis of IgG was disrupted, lipid absorption was perturbed, and neonatal mice died within days of birth. These data highlight the important roles of the Arp2/3 complex in vesicle trafficking in enterocytes and suggest that defects in cytoplasmic F-actin assembly by the Arp2/3 complex, rather than cortical pools, underlie many of the phenotypes seen in the mutant small intestine.

Indexed as

Actin-Related Protein 2-3 ComplexActinsAnimalsEndosomesGene Knockout TechniquesImmunoglobulin GIntestinal AbsorptionIntestinal MucosaIntestine, SmallLipid MetabolismMiceTranscytosisActin-Related Protein 2-3 ComplexActinsArpc3 protein, mouseImmunoglobulin G

Identifiers

PMID25833710
PMCPMC4472011
OpenAlexW2003591869

What OpenQuestion holds

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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 OpenQuestion graph.