Evidence map›Paper›PMID 11294904›Full record

ArticleMolecular biology of the cell2001

Endothelial transcytotic machinery involves supramolecular protein-lipid complexes.

S A Predescu, D N Predescu, G E Palade

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

33 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Lung Endothelial Transcytosis.Comprehensive Physiology · 2020
    Review
  7. Neutrophil-endothelial interactions of murine cells is not a good predictor of their interactions in human cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Endothelial membrane reorganization during leukocyte extravasation.Cellular and molecular life sciences : CMLS · 2012
    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.

S A PredescuDepartment of Cellular and Molecular Medicine, School of Medicine, University of California, San Diego, La Jolla 92093, USA. spredescu@ucsd.edu
D N Predescu
G E Palade
University of California San Diego · US

Funding

LOCATION OF PORE SYSTEMS IN CAPILLARY WALLSR01HL017080 · NHLBI · YALE UNIVERSITY · PI PALADE, GEORGE E · 1985 to 2000
$344k
LOCATION OF PORE SYSTEMS IN CAPILLARY WALLSR37HL017080 · NHLBI · YALE UNIVERSITY · PI PALADE, GEORGE E · 1987 to 1996
–
NHLBI NIH HHS HL-17080
6 · The paper itself

Abstract

We have demonstrated that the plasmalemmal vesicles (caveolae) of the continuous microvascular endothelium function as transcytotic vesicular carriers for protein molecules > 20 A and that transcytosis is an N-ethylmaleimide-sensitive factor (NSF)-dependent, N-ethylmaleimide-sensitive process. We have further investigated NSF interactions with endothelial proteins to find out 1) whether a complete set of fusion and targeting proteins is present in the endothelium; 2) whether they are organized in multimolecular complexes as in neurons; and 3) whether the endothelial multimolecular complexes differ from their neuronal counterparts, because of their specialized role in transcytosis. To generate the complexes, we have used myc-NSF, cultured pulmonary endothelial cells, and rat lung cytosol and membrane preparations; to detect them we have applied coimmunoprecipitation with myc antibodies; and to characterize them we have used velocity sedimentation and cross-linking procedures. We have found that both cytosolic and membrane fractions contain complexes that comprise beside soluble NSF attachment proteins and SNAREs (soluble NSF attachment protein receptor), rab 5, dynamin, caveolin, and lipids. By immunogold labeling and negative staining we have detected in these complexes, myc-NSF, syntaxin, dynamin, caveolin, and endogenous NSF. Similar complexes are formed by endogenous NSF. The results indicate that complexes with a distinct protein-lipid composition exist and suggest that they participate in targeting, fusion, and fission of caveolae with the endothelial plasmalemma.

Indexed as

Lipid MetabolismVesicular Transport ProteinsAnimalsBiological TransportCarrier ProteinsCaveolin 1CaveolinsCells, CulturedCross-Linking ReagentsCytosolEndothelium, VascularEthylmaleimideHumansMacromolecular SubstancesMembrane ProteinsMicroscopy, Electronbis(sulfosuccinimidyl)tartrateCarrier ProteinsCAV1 protein, humanCav1 protein, ratCaveolin 1CaveolinsCross-Linking ReagentsEthylmaleimideMacromolecular SubstancesMembrane ProteinsN-Ethylmaleimide-Sensitive ProteinsNsf protein, ratProteinsQa-SNARE ProteinsRecombinant Fusion ProteinsSuccinimidesVesicle-Associated Membrane Protein 3Vesicular Transport Proteins

Identifiers

PMID11294904
PMCPMC32284
OpenAlexW2170866255

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.