Evidence map›Paper›PMID 9788954›Full record

ArticleBiophysical journal1998

Membrane capacitance changes associated with particle uptake during phagocytosis in macrophages.

K O Holevinsky, D J Nelson

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

34 citing papers in PubMed, 100 citations in OpenAlex.

  1. Phagocytosis at a glance.Journal of cell science · 2025
    Review
  2. Frontiers in microbiology · 2025
    Article
  3. Biomechanics of phagocytosis of red blood cells by macrophages in the human spleen.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Article
  5. Article
  6. Origins of eukaryotic excitability.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Review
  7. Examining the Underappreciated Role ofFrontiers in immunology · 2021
    Review
  8. Article
  9. Article
  10. Review
  11. CaThe Journal of biological chemistry · 2017
    Article
  12. Review
  13. Lysosomal exocytosis and lipid storage disorders.Journal of lipid research · 2014
    Review
  14. The cell surface proteome of Entamoeba histolytica.Molecular & cellular proteomics : MCP · 2014
    Article
  15. Article
  16. Plasma membrane tension orchestrates membrane trafficking, cytoskeletal remodeling, and biochemical signaling during phagocytosis.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  17. Article
  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

2 authors at 1 institution in 1 country.

K O HolevinskyDepartment of Pharmacological and Physiological Sciences, The University of Chicago, Chicago, Illinois 60637, USA.
D J Nelson
University of Chicago · US

Funding

ROLE OF ION CHANNELS IN MONONUCLEAR PHAGOCYTE ACTIVATIONR01GM036823 · NIGMS · UNIVERSITY OF CHICAGO · PI NELSON, DEBORAH J. · 1986 to 2012
$3.2M
MUSCARINIC GATED ATRIAL K+ CHANNELR01GM054266 · NIGMS · UNIVERSITY OF CHICAGO · PI NELSON, DEBORAH J. · 1996 to 1999
–
NIGMS NIH HHS R01 GM36823NIGMS NIH HHS R01 GM54266
6 · The paper itself

Abstract

We report the use of capacitance measurements to monitor particle uptake after cellular exposure to phagocytic stimuli. In these studies, human monocyte-derived macrophages (HMDMs) and cells from the murine macrophage-like cell line J774.1 were exposed to immune complexes or sized latex particles (0.8 or 3.2 micron in diameter). An average decrease in cell capacitance of 8 pF was seen after exposure of the cells to immune complexes. Cells in which particle uptake was inhibited by cytochalasin B treatment before exposure to immune complexes showed an average increase of 0.5 pF. The decrease in membrane capacitance after exposure of cells to particulate stimuli was absent with the soluble stimulus, platelet-activating factor, further confirming that decreases in membrane capacitance were due to particle uptake. Exposure of cells to sized latex particles resulted in a graded, stepwise decrease in membrane capacitance. The average step size for 0.8-micron particles was 250 fF, and the average step change for the larger 3.2-micron particles was 480 fF, as calculated from Gaussian fits to the step size amplitude histograms. The predicted step size for the individual particles based upon the minimum amount of membrane required to enclose a particle and a specific capacitance of 10 fF/micron2 was 20 and 320 fF, respectively. The step size for the smaller particles deviates significantly from the predicted size distribution, indicating either a possible lower limit to the size of the phagocytic vacuole or multiple particles taken up within a single phagosome. Dynamic interaction between phagocytosis and exocytosis was observed in a number of cells as a biphasic response consisting of an initial rapid increase in capacitance, consistent with cellular exocytosis, followed by stepwise decreases in capacitance.

Indexed as

Electric ConductivityAnimalsAntigen-Antibody ComplexCell MembraneCytochalasin BElectrophysiologyExocytosisHumansLatexMacrophagesMiceMicrospheresParticle SizePhagocytosisPhagosomesAntigen-Antibody ComplexCytochalasin BLatex

Identifiers

PMID9788954
PMCPMC1299933
OpenAlexW2011541372

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.