Cited by 188Cellular Mechanics and InteractionsCellular transport and secretionLipid Membrane Structure and Behavior

Control of cell membrane tension by myosin-I

Open access
Nambiar, Rajalakshmi, McConnell, Russell E., Tyska, Matthew J.·2009·Proceedings of the National Academy of Sciences

Abstract

All cell functions that involve membrane deformation or a change in cell shape (e.g., endocytosis, exocytosis, cell motility, and cytokinesis) are regulated by membrane tension. While molecular contacts between the plasma membrane and the underlying actin cytoskeleton are known to make significant contributions to membrane tension, little is known about the molecules that mediate these interactions. We used an optical trap to directly probe the molecular determinants of membrane tension in isolated organelles and in living cells. Here, we show that class I myosins, a family of membrane-binding, actin-based motor proteins, mediate membrane/cytoskeleton adhesion and thus, make major contributions to membrane tension. These studies show that class I myosins directly control the mechanical properties of the cell membrane; they also position these motor proteins as master regulators of cellular events involving membrane deformation.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1073/pnas.0901641106

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

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?

  • Alternative perturbations such as mechanical stretching, RhoA-ROCK activation, or modification of lipid composition can induce significant disruption ranging from membrane-cytoskeleton decoupling, contractility-induced retraction to altered lipid composition and gene expression.

    “Alternative perturbations such as mechanical stretching73, RhoA-ROCK activation74–76, or the modification of lipid composition77 can induce significant disruption ranging from membrane-cytoskeleton decoupling, contractility-induced retraction to altered lipid composition and gene expression.”

    From Ghost Neuron preparation unlocks high-resolution structural mapping of intracellular architecture in axons (2026) · cites this paper as [76]

    Split into 2 atoms — 0 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 1 unverifiable. Expand the claim to see per-atom verdicts.

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cited by

Sorted by citations

Authors
Nambiar, R., McConnell, R. E., & Tyska, M. J.
Affiliations
  • Vanderbilt University Medical Center (US)
  • National Heart, Lung, and Blood Institute (US)
Corresponding author
Tyska, Matthew J.
Venue
Proceedings of the National Academy of Sciences
Published
2009-07-21
Volume
106
Issue
29
Pages
11972-11977
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2034863887
Cited by
188
References
0
Citations by year
2026: 9 · 2025: 5 · 2024: 4 · 2023: 6 · 2022: 19 · 2021: 12 · 2020: 11 · 2019: 8 · 2018: 12 · 2017: 6 · 2016: 13 · 2015: 11 · 2014: 16 · 2013: 9 · 2012: 15
FWCI
6.36
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • American Heart Association
  • Vanderbilt University
  • Vanderbilt University Medical Center
  • National Institutes of Health (P30 DK)
  • Vanderbilt Digestive Diseases Research Center, Vanderbilt University Medical Center
  • National Institute of Diabetes and Digestive and Kidney Diseases (R01DK075555, P30DK058404)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (T32HD007502)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Lipid Membrane Structure and Behavior
Keywords
membrane tension, myosin I, class I myosin, actin cytoskeleton, membrane deformation, optical trapping, organelles, cell mechanics, motor proteins
MeSH terms
Animals, Biomechanical Phenomena, Cell Adhesion, Cell Membrane, Cell Survival, Cytoskeleton, Epithelial Cells, Fibroblasts, Microvilli, Recombinant Fusion Proteins, Transfection, Mice, Knockout, Microscopy, Confocal, Myosin Heavy Chains, NIH 3T3 Cells, Green Fluorescent Proteins, Mice, Optical Tweezers

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review