Evidence map›Paper›PMID 1993739›Full record

ArticleThe Journal of cell biology1991

Low viscosity in the aqueous domain of cell cytoplasm measured by picosecond polarization microfluorimetry.

K Fushimi, A S Verkman

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of cell biology, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

65 citing papers in PubMed, 254 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Article
  7. Review
  8. The Thermodynamics of Medial Vascular Calcification.Frontiers in cell and developmental biology · 2021
    Review
  9. Challenges for biophysical modeling of microstructure.Journal of neuroscience methods · 2020
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Non-invasive Neurite Mechanics in Differentiated PC12 Cells.Frontiers in cellular neuroscience · 2018
    Article
  19. Article
  20. Article

5 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

K FushimiDepartment of Medicine, University of California, San Francisco 94143-0532.
A S Verkman
University of California, San Francisco · US

Funding

MECHANISMS OF WATER TRANSPORT IN RENAL EPITHELIAR37DK035124 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VERKMAN, ALAN S · 1999 to 2008
$4.2M
WATER AND NON-ELECTROLYTE TRANSPORT IN RENAL VESICLESR01DK035124 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VERKMAN, ALAN S · 1986 to 2014
$1.4M
SINGLE CHANNEL KINETICS OF WILD-TYPE AND MUTANT CFTRP50HL042368 · NHLBI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI FINKBEINER, WALTER E · 1988 to 1997
–
DEVELOPMENT OF CHLORIDE-SENSITIVE FLUORESCENT INDICATORSR01DK039354 · NIDDK · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI VERKMAN, ALAN S · 1988 to 1991
–
NHLBI NIH HHS HL42368NIDDK NIH HHS DK35124NIDDK NIH HHS DK39354
6 · The paper itself

Abstract

Information about the rheological characteristics of the aqueous cytoplasm can be provided by analysis of the rotational motion of small polar molecules introduced into the cell. To determine fluid-phase cytoplasmic viscosity in intact cells, a polarization microscope was constructed for measurement of picosecond anisotropy decay of fluorescent probes in the cell cytoplasm. We found that the rotational correlation time (tc) of the probes, 2,7-bis-(2-carboxyethyl)-5-(and-6-)carboxyfluorescein (BCECF), 6-carboxyfluorescein, and 8-hydroxypyrene-1,3,6-trisulfonic acid (HPTS) provided a direct measure of fluid-phase cytoplasmic viscosity that was independent of probe binding. In quiescent Swiss 3T3 fibroblasts, tc values were 20-40% longer than those in water, indicating that the fluid-phase cytoplasm is only 1.2-1.4 times as viscous as water. The activation energy of fluid-phase cytoplasmic viscosity was 4 kcal/mol, which is similar to that of water. Fluid-phase cytoplasmic viscosity was altered by less than 10% upon addition of sucrose to decrease cell volume, cytochalasin B to disrupt cell cytoskeleton, and vasopressin to activate phospholipase C. Nucleoplasmic and peripheral cytoplasmic viscosities were not different. Our results establish a novel method to measure fluid-phase cytoplasmic viscosity, and indicate that fluid-phase cytoplasmic viscosity in fibroblasts is similar to that of free water.

Indexed as

AnimalsCell DivisionCell NucleusCells, CulturedCytophotometryCytoplasmCytoskeletonEnzyme ActivationFluorescence PolarizationFluorescent DyesTemperatureType C PhospholipasesViscosityFluorescent DyesType C Phospholipases

Identifiers

PMID1993739
PMCPMC2288848
OpenAlexW2116043125

What OpenQuestion holds

Textmetadata
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.