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Cited by 73Metabolism, Diabetes, and CancerCellular transport and secretionGrowth Hormone and Insulin-like Growth Factors

The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.

Regulation of cell surface GLUT1, GLUT3, and GLUT4 by insulin and IGF‐I in L6 myotubes

Wilson, Cindy M., Mitsumoto, Yasuhide, Maher, Fran, Klip, Amira·1995·FEBS Letters
DOI 10.1016/0014-5793(95)00589-2
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Abstract

The effects of insulin and IGF‐I on the cell surface quantities of GLUT1, GLUT3 and GLUT4 glucose transporters in L6 myotubes were determined with the exofacial bis‐mannose phololabel (ATB‐BMPA). In basal cells, an equal molar quantity of each transporter isoform was found at the cell surface. Insulin stimulated the translocation of all three glucose transporter isoforms to the plasma membrane fraction from the light microsome fraction, resulting in equal molar quantities on the cell surface. IGF‐I stimulated a similar translocation of all isoforms, augmented by an increase in surface GLUT3 as assessed by ATB‐BMPA.

Overview

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Registry

Crossref · 10.1016/0014-5793(95)00589-2

Cites

19 of 19 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Insulin stimulates translocation of GLUTs from intracellular pools to the cell membrane, amplifying glucose uptake from blood into fat and skeletal muscle cells.

    “a process that is amplified by the translocation of GLUTs from intracellular pools to the cell membrane following insulin stimulation ( 26, 27 ).”

    From Dynamic modulation of glucose utilisation by glucocorticoid rhythms in health and disease (2020) · cites this paper as [27]

  • Kinetic rates involved in GLUT translocation, including the effects of insulin and glucocorticoids, were estimated from prior studies.

    “the kinetic rates involved in the translocation of GLUT transporters, including the effects of insulin and glucocorticoids, were estimated from ( 27, 34, 46 );”

    From Dynamic modulation of glucose utilisation by glucocorticoid rhythms in health and disease (2020) · cites this paper as [27]

Citations

Cites

Flagged first, then by citations

Research works printed but not linked: 2

  1. Mitsumoto Y., 1990, Biochem. Biophys. Res. Commun., 175
  2. 1968, Proc. Natl. Acad. Sci. USA, 477

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Metadata

Authors
Wilson, C. M., Mitsumoto, Y., Maher, F., & Klip, A.
Affiliations
  • National Institutes of Health (US)
  • Hospital for Sick Children (CA)
ORCID
Venue
FEBS Letters
Publisher
Wiley
Published
1995-07-10
Volume
368
Issue
1
Pages
19-22
ISSN
  • 0014-5793 (ISSN-L)
  • 1873-3468
DOI
10.1016/0014-5793(95)00589-2
OpenAlex
W1979543751
Cited by
73
References
19
Citations by year
2021: 1 · 2020: 2 · 2019: 1 · 2018: 1 · 2017: 2 · 2015: 2 · 2014: 3 · 2013: 2 · 2012: 6
FWCI
1.11
Type
journal article
Language
en
Open access
closed
Licence
onlinelibrary.wiley.com/termsAndConditions#vor (vor, 1702 d)
Locations
  • FEBS Letters (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Growth Hormone and Insulin-like Growth Factors
Keywords
GLUT1, GLUT3, GLUT4, glucose transporters, insulin, insulin-like growth factor I, L6 myotubes, cell surface, plasma membrane, skeletal muscle
MeSH terms
Affinity Labels, Animals, Azides, Cell Line, Cell Membrane, Disaccharides, Glucose, Glycosides, Humans, Insulin, Insulin-Like Growth Factor I, Monosaccharide Transport Proteins, Muscle Proteins, Nerve Tissue Proteins, Propylamines, Muscle, Skeletal, Glucose Transporter Type 1, Glucose Transporter Type 3, Glucose Transporter Type 4, Mice

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