Evidence map›Paper›PMID 10077560›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Structural characteristics of supramolecular assemblies formed by guanidinium-cholesterol reagents for gene transfection.

B Pitard, N Oudrhiri, J P Vigneron, M Hauchecorne, O Aguerre, R Toury, M Airiau, R Ramasawmy, D Scherman, J Crouzet and 2 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 95 citations in OpenAlex.

  1. Review
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  14. Structural investigations of DNA-polycation complexes.The European physical journal. E, Soft matter · 2005
    Article
  15. Article
  16. Article
  17. Article
  18. Reducible cationic lipids for gene transfer.The Biochemical journal · 2001
    Article
  19. Article
  20. Vectors for gene therapy of cardiovascular disease.Current cardiology reports · 2000
    Review
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

12 authors at 1 institution in 1 country.

B PitardUnité Mixte de Recherche, 133 Rhône-Poulenc Rorer, Centre National de la Recherche Scientifique, France. bruno.pitard@rp-rorer.fr
N Oudrhiri
J P Vigneron
M Hauchecorne
O Aguerre
R Toury
M Airiau
R Ramasawmy
D Scherman
J Crouzet
J M Lehn
P Lehn
Collège de France · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have recently discovered that cationic cholesterol derivatives characterized by guanidinium polar headgroups are very efficient for gene transfection in vitro and in vivo. In spite of being based on some rationale at the molecular level, the development of these new synthetic vectors was nevertheless empirical. Indeed, the factors and processes underlying cationic lipid-mediated gene transfer are still poorly understood. Thus, to get a better insight into the mechanisms involved, we have examined the supramolecular structure of lipid/DNA aggregates obtained when using reagent bis(guanidinium)-tren-cholesterol (BGTC), either alone or as a liposomal formulation with the neutral phospholipid dioleoyl phosphatidylethanolamine (DOPE). We here report the results of cryotransmission electron microscopy studies and small-angle x-ray scattering experiments, indicating the presence of multilamellar domains with a regular spacing of 70 A and 68 A in BGTC/DOPE-DNA and BGTC-DNA aggregates, respectively. In addition, DNA lipoplexes with similar lamellar patterns were detected inside transfected HeLa cells by conventional transmission electron microscopy. These results suggest that DNA condensation by multivalent guanidinium-cholesterol cationic lipids involves the formation of highly ordered multilamellar domains, the DNA molecules being intercalated between the lipid bilayers. These results also invite further investigation of the intracellular fate of the internalized lipid/DNA structures during their trafficking toward the cell nucleus. The identification of the basic features of active complexes should indeed help in the design of improved guanidinium-based vectors.

Indexed as

Gene Transfer TechniquesCholesterolDNAGenetic VectorsGuanidineHeLa CellsHumansMicroscopy, ElectronX-Ray DiffractionCholesterolDNAGuanidine

Identifiers

PMID10077560
PMCPMC15818
OpenAlexW1974854895

What OpenQuestion holds

Texttitle and abstract
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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.