Evidence map›Paper›PMID 11160828›Full record

ArticleMolecular biology of the cell2001

Insulin action on GLUT4 traffic visualized in single 3T3-l1 adipocytes by using ultra-fast microscopy.

V Patki, J Buxton, A Chawla, L Lifshitz, K Fogarty, W Carrington, R Tuft, S Corvera

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 109 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Microtubules in insulin action: what's on the tube?Trends in endocrinology and metabolism: TEM · 2021
    Review
  8. Article
  9. InducibleThe Journal of biological chemistry · 2019
    Article
  10. Article
  11. The Mechanism of Phillyrin from the Leaves ofBioMed research international · 2019
    Article
  12. Article
  13. Review
  14. Review
  15. Regulation of glucose transport by insulin: traffic control of GLUT4.Nature reviews. Molecular cell biology · 2012
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Targeted disruption of ROCK1 causes insulin resistance in vivo.The Journal of biological chemistry · 2009
    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

8 authors at 2 institutions in 2 countries.

V PatkiDepartment of Cell Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
J Buxton
A Chawla
L Lifshitz
K Fogarty
W Carrington
R Tuft
S Corvera
University of Massachusetts Chan Medical School · USInstitute of Molecular and Cell Biology · RU

Funding

PILOT AND FEASIBILITY PROGRAMP30DK032520 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1986 to 2010
$14.6M
NIDDK NIH HHS DK-32520NIDDK NIH HHS P30 DK032520
6 · The paper itself

Abstract

A novel imaging technology, high-speed microscopy, has been used to visualize the process of GLUT4 translocation in response to insulin in single 3T3-L1 adipocytes. A key advantage of this technology is that it requires extremely low light exposure times, allowing the quasi-continuous capture of information over 20-30 min without photobleaching or photodamage. The half-time for the accumulation of GLUT4-eGFP (enhanced green fluorescent protein) at the plasma membrane in a single cell was found to be of 5-7 min at 37 degrees C. This half-time is substantially longer than that of exocytic vesicle fusion in neuroendocrine cells, suggesting that additional regulatory mechanisms are involved in the stimulation of GLUT4 translocation by insulin. Analysis of four-dimensional images (3-D over time) revealed that, in response to insulin, GLUT4-eGFP-enriched vesicles rapidly travel from the juxtanuclear region to the plasma membrane. In nontransfected adipocytes, impairment of microtubule and actin filament function inhibited insulin-stimulated glucose transport by 70 and 50%, respectively. When both filament systems were impaired insulin-stimulated glucose transport was completely inhibited. Taken together, the data suggest that the regulation of long-range motility of GLUT4-containing vesicles through the interaction with microtubule- and actin-based cytoskeletal networks plays an important role in the overall effect of insulin on GLUT4 translocation.

Indexed as

Muscle Proteins3T3 CellsAdipocytesAnimalsCytoskeletonDiagnostic ImagingExocytosisGlucose Transporter Type 4Green Fluorescent ProteinsHalf-LifeInsulinLuminescent ProteinsMiceMicroscopy, ConfocalMonosaccharide Transport ProteinsProtein TransportGlucose Transporter Type 4Green Fluorescent ProteinsInsulinLuminescent ProteinsMonosaccharide Transport ProteinsMuscle ProteinsRecombinant Fusion ProteinsSlc2a4 protein, mouseSlc2a4 protein, rat

Identifiers

PMID11160828
PMCPMC30573
OpenAlexW2067309238

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.