Evidence map›Paper›PMID 16448225›Full record

ArticleIn vitro cellular & developmental biology. Animal

Melittin-induced membrane permeability: a nonosmotic mechanism of cell death.

Juan Pablo Pratt, Dino J Ravnic, Harold T Huss, Xiaoqun Jiang, Benjamin S Orozco, Steven J Mentzer

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 33 citations in OpenAlex.

  1. Dual-Modified Liposome for Targeted and Enhanced Gene Delivery into Mice Brain.The Journal of pharmacology and experimental therapeutics · 2020
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Melittin-glutathione S-transferase fusion protein exhibits anti-inflammatory properties and minimal toxicity.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2014
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. A new potent secondary amphipathic cell-penetrating peptide for siRNA delivery into mammalian cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2009
    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

6 authors at 2 institutions in 1 country.

Juan Pablo PrattLaboratory of Immunophysiology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Dino J Ravnic
Harold T Huss
Xiaoqun Jiang
Benjamin S Orozco
Steven J Mentzer
Brigham and Women's Hospital · USHarvard University · US

Funding

Microangiectasia Regulation of Lymphocyte MigrationR01HL047078 · NHLBI · DANA-FARBER CANCER INSTITUTE · PI MENTZER, STEVEN · 1997 to 2006
$2.1M
Physiology of Systemic and Pulmonary MicroangiectasiasR01HL075426 · NHLBI · DANA-FARBER CANCER INSTITUTE · PI MENTZER, STEVEN · 2003 to 2006
$1.4M
LYMPHOCYTE RECRUITMENT IN LUNG TRANSPLATATIONR29HL047078 · NHLBI · DANA-FARBER CANCER INSTITUTE · PI MENTZER, STEVEN J · 1992 to 1995
–
NHLBI NIH HHS HL47078NHLBI NIH HHS HL75426
6 · The paper itself

Abstract

Derived from honeybees, melittin is a 26-amino acid, alpha-helical, membrane-attack protein that efficiently kills mammalian cells. To investigate the contribution of colloid-osmotic effects to the mechanism of cell death, we studied the effect of melittin on lymphocyte membrane permeability and cell volumes. Melittin concentrations of 0.5 to 2.0 microM induced release of membrane permeability markers without total disruption of the cell membrane. At these melittin concentrations, electrical-impedance cytometry demonstrated melittin-induced changes in red blood cell volumes (P<0.01), but no change in lymphocyte cell volumes (P>0.05). Streaming video microscopy, obtaining images of melittin-treated lymphocytes at 80-ms intervals, demonstrated a loss of optical density (P<0.001) suggesting a flattening of the cell but no significant increase in cell perimeter (P>0.05). Real-time multiparameter flow cytometry of melittin-treated lymphocytes confirmed simultaneous loss of the cytoplasmic marker, calcein, and uptake of the DNA dye, ethidium homodimer, but demonstrated no increase in forward light scatter. Transmission-electron microscopy of melittin-treated lymphocytes showed normal cell volumes but discontinuities in the cell membrane suggesting direct membrane toxicity. We conclude that melittin causes lymphocyte death by a "leaky patch" mechanism that is independent of colloid-osmotic effects.

Indexed as

AnimalsApoptosisBeesCell Membrane PermeabilityCell SizeDose-Response Relationship, DrugErythrocytesFlow CytometryLymphocytesMelittenMicroscopy, Electron, TransmissionMicroscopy, VideoMelitten

Identifiers

PMID16448225
OpenAlexW1814847662

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.