Evidence map›Paper›PMID 7540430›Full record

ArticleBiophysical journal1995

Cell volume measured by total internal reflection microfluorimetry: application to water and solute transport in cells transfected with water channel homologs.

J Farinas, V Simanek, A S Verkman

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 69 citations in OpenAlex.

  1. Methods to Measure Water Permeability.Advances in experimental medicine and biology · 2023
    Article
  2. Determination of cell volume as part of metabolomics experiments.American journal of physiology. Cell physiology · 2021
    Article
  3. Article
  4. Article
  5. Article
  6. Aquaporins: important but elusive drug targets.Nature reviews. Drug discovery · 2014
    Review
  7. Article
  8. Modelling the swelling assay for aquaporin expression.Journal of mathematical biology · 2008
    Article
  9. Article
  10. Functional involvement of Annexin-2 in cAMP induced AQP2 trafficking.Pflugers Archiv : European journal of physiology · 2008
    Article
  11. Article
  12. Comparative functional analysis of aquaporins/glyceroporins in mammals and anurans.Mammalian genome : official journal of the International Mammalian Genome Society · 2007
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Evanescent-wave microscopy: a new tool to gain insight into the control of transmitter release.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 1999
    Review
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

J FarinasDepartment of Medicine, University of California, San Francisco 94143-0521, USA.
V Simanek
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
APPLICATION OF NOVEL OPTICAL METHODS TO CELL DYNAMICSR01DK043840 · NIDDK · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI VERKMAN, ALAN S · 1993 to 2001
$494k
NIDDK NIH HHS DK35124NIDDK NIH HHS DK43840
6 · The paper itself

Abstract

Total internal reflection (TIR) microfluorimetry was established as a method to measure continuously the volume of adherent cells and applied to measure membrane permeabilities in cells transfected with water channel homologs. Cytosol was labeled with the membrane-impermeant fluorophore calcein. Fluorescence was excited by the TIR evanescent field in a thin section of cytosol (approximately 150 nm) adjacent to the cell-substrate interface. Because cytosolic fluorophore number per cell remains constant, the TIR fluorescence signal should be inversely related to cell volume. For small volume changes in Sf-9 and LLC-PK1 cells, relative TIR fluorescence was nearly equal to inverse relative cell volume; deviations from the ideal were modeled theoretically. To measure plasma membrane osmotic water permeability, Pf, the time course of osmotically induced cell volume change was inferred from the TIR fluorescence signal. LLC-PK1 cells expressing the CHIP28 water channel had an HgCl2-sensitive, threefold increase in Pf compared to nontransfected cells (Pf = 0.0043 cm/s at 10 degrees C). Solute permeability was measured from the TIR fluorescence time course in response to solute gradients. Glycerol permeability in Sf-9 cells expressing the water channel homolog GLIP was (1.3 +/- 0.2) x 10(-5) cm/s (22 degrees C), greater than that of (0.36 +/- 0.04) x 10(-5) cm/s (n = 4, p < 0.05) for control cells, indicating functional expression of GLIP. Water and urea permeabilities were similar in GLIP-expressing and control cells. The TIR method should be applicable to the study of water and solute permeabilities and cell volume regulation in cells of arbitrary shape and size.

Indexed as

AquaporinsCell SizeAnimalsAntiportersAquaporin 1Biological Transport, ActiveBiophysical PhenomenaBiophysicsCell LineCell Membrane PermeabilityFluorometryIon ChannelsLLC-PK1 CellsModels, BiologicalOsmolar ConcentrationSpodopteraAntiportersAquaporin 1Aquaporinsglycerol intrinsic protein, ratIon ChannelsWater

Identifiers

PMID7540430
PMCPMC1282057
OpenAlexW2014749038

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.