Evidence map›Paper›PMID 12937987›Full record

ArticlePflugers Archiv : European journal of physiology2003

Measurement of rapid changes in cell volume by forward light scattering.

S P Srinivas, Joseph A Bonanno, Els Larivière, Danny Jans, Willy Van Driessche

Abstract read
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. CLN3 loss disturbs membrane microdomain properties and protein transport in brain endothelial cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  4. Article
  5. Article
  6. Article
  7. Dynamic regulation of barrier integrity of the corneal endothelium.Optometry and vision science : official publication of the American Academy of Optometry · 2010
    Review
  8. Article
  9. Lack of threshold for anisotonic cell volume regulation.The Journal of membrane biology · 2006
    Article
  10. Optophysiology: depth-resolved probing of retinal physiology with functional ultrahigh-resolution optical coherence tomography.Proceedings of the National Academy of Sciences of the United States of America · 2006
    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

5 authors at 2 institutions in 2 countries.

S P SrinivasSchool of Optometry, Indiana University, Bloomington, IN 47405, USA.
Joseph A Bonanno
Els Larivière
Danny Jans
Willy Van Driessche
KU Leuven · BEIndiana University · US

Funding

REGULATION OF PHI AND FLUID FLUX IN CORNEAL ENDOTHELIUMR01EY008834 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI BONANNO, JOSEPH AURELIO · 1991 to 2020
$7.8M
VOLUME REGULATION IN CORNEAL ENDOTHELIUMR01EY011107 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI SRINIVAS, SANGLY P · 1995 to 2002
$589k
NEI NIH HHS EY00834NEI NIH HHS R01 EY008834PHS HHS E11107
6 · The paper itself

Abstract

Light scattering is an empirical technique employed to measure rapid changes in cell volume. This study describes a new configuration for the method of light scattering and its corroboration by measurements of cell height (as a measure of cell volume). Corneal endothelial cells cultured on glass cover-slips were mounted in a perfusion chamber on the stage of an inverted microscope. A beam of light was focused on the cells from above the stage at an angle of 40 degrees to the plane of the stage. The scattered light intensity (SLI), captured by the objective and referred to as forward light scatter (FLS), increased and decreased in response to hyposmotic and hyperosmotic shocks, respectively. The rapid increase and decrease in SLI corresponded to cell swelling and shrinkage, respectively. Subsequently, SLI decreased and increased as expected for a regulatory volume decrease (RVD) and increase (RVI), respectively. These data are in agreement with measurements of cell height, demonstrating that the method of light scatter in FLS mode is useful for monitoring rapid changes in cell volume of cultured cells. Changes in SLI caused by gramicidin were consistent with cell volume changes induced by equilibration of NaCl and KCl concentrations across the cell membrane. Similarly, an additional decrease in SLI was recorded during RVD upon increasing K+ conductance by valinomycin. Decreasing K+ conductance of the cell membrane with Ba2+ changed the time course of SLI consistent with the effect of the K+ channel blocker on RVD. Bumetanide and dihydro-ouabain inhibited increases in SLI during RVI. In conclusion, FLS is a valid method for qualitative analysis of cell volume changes with a high time resolution.

Indexed as

LightAnimalsCattleCell SizeEndothelial CellsResearch DesignScattering, Radiation

Identifiers

PMID12937987
PMCPMC4118695
OpenAlexW1969479040

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.