Evidence map›Paper›PMID 19324878›Full record

ArticleThe Journal of biological chemistry2009

Membrane permeabilization by trypanosome lytic factor, a cytolytic human high density lipoprotein.

John M Harrington, Sawyer Howell, Stephen L Hajduk

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. APOL1 and kidney cell function.American journal of physiology. Renal physiology · 2019
    Review
  6. Review
  7. Article
  8. Article
  9. The Cell Biology of APOL1.Seminars in nephrology · 2017
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. APOL1 localization in normal kidney and nondiabetic kidney disease.Journal of the American Society of Nephrology : JASN · 2011
    Article
  19. Review
  20. Mechanism of Trypanosoma brucei gambiense (group 1) resistance to human trypanosome lytic factor.Proceedings of the National Academy of Sciences of the United States of America · 2010
    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.

John M HarringtonDepartment of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia 30602.
Sawyer HowellDepartment of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia 30602.
Stephen L HajdukDepartment of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia 30602. Electronic address: shajduk@bmb.uga.edu.
University of Georgia · US

Funding

Trypanosome Lysis by Human Haptoglobin Related ProteinR01AI039033 · NIAID · UNIVERSITY OF GEORGIA · PI HAJDUK, STEPHEN L · 1996 to 2014
$3.5M
Lysis of Trypanosomes by Haptoglobin Related ProteinR21AI039033 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HAJDUK, STEPHEN L · 2001 to 2001
$287k
NIAID NIH HHS AI39033
6 · The paper itself

Abstract

Trypanosome lytic factor (TLF) is a subclass of human high density lipoprotein (HDL) that mediates an innate immune killing of certain mammalian trypanosomes, most notably Trypanosoma brucei brucei, the causative agent of a wasting disease in cattle. Mechanistically, killing is initiated in the lysosome of the target trypanosome where the acidic pH facilitates a membrane-disrupting activity by TLF. Here we utilize a model liposome system to characterize the membrane binding and permeabilizing activity of TLF and its protein constituents, haptoglobin-related protein (Hpr), apolipoprotein L-1 (apoL-1), and apolipoprotein A-1 (apoA-1). We show that TLF efficiently binds and permeabilizes unilamellar liposomes at lysosomal pH, whereas non-lytic human HDL exhibits inefficient permeabilizing activity. Purified, delipidated Hpr and apoL-1 both efficiently permeabilize lipid bilayers at low pH. Trypanosome lytic factor, apoL-1, and apoA-1 exhibit specificity for anionic membranes, whereas Hpr permeabilizes both anionic and zwitterionic membranes. Analysis of the relative particle sizes of susceptible liposomes reveals distinctly different membrane-active behavior for native TLF and the delipidated protein components. We propose that lysosomal membrane damage in TLF-susceptible trypanosomes is initiated by the stable association of the TLF particle with the lysosomal membrane and that this is a property unique to this subclass of human HDL.

Indexed as

Models, BiologicalAnimalsAntigens, NeoplasmApolipoprotein L1ApolipoproteinsCattleHaptoglobinsHumansHydrogen-Ion ConcentrationImmunity, InnateLipid BilayersLipoproteins, HDLLiposomesLysosomesSpecies SpecificityTrypanosoma brucei bruceiAntigens, NeoplasmAPOL1 protein, humanApolipoprotein L1ApolipoproteinsHaptoglobinsHPR protein, humanLipid BilayersLipoproteins, HDLLiposomesTLF1 protein, human

Identifiers

PMID19324878
PMCPMC2679451
OpenAlexW2028924923

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.