Evidence map›Paper›PMID 17071747›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

CLA-1 and its splicing variant CLA-2 mediate bacterial adhesion and cytosolic bacterial invasion in mammalian cells.

Tatyana G Vishnyakova, Roger Kurlander, Alexander V Bocharov, Irina N Baranova, Zhigang Chen, Mones S Abu-Asab, Maria Tsokos, Daniela Malide, Federica Basso, Alan Remaley and 3 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. 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
1.8field-weighted citation impact, top 15% 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, 74 citations in OpenAlex.

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  14. Formation of a protein corona on silver nanoparticles mediates cellular toxicity via scavenger receptors.Toxicological sciences : an official journal of the Society of Toxicology · 2015
    Article
  15. Article
  16. Scavenger receptor class B type I and immune dysfunctions.Current opinion in endocrinology, diabetes, and obesity · 2014
    Review
  17. Article
  18. Article
  19. Crosstalk between reverse cholesterol transport and innate immunity.Trends in endocrinology and metabolism: TEM · 2012
    Review
  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

13 authors at 5 institutions in 2 countries.

Tatyana G VishnyakovaLight Microscopy Core Facility, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Roger Kurlander
Alexander V Bocharov
Irina N Baranova
Zhigang Chen
Mones S Abu-Asab
Maria Tsokos
Daniela Malide
Federica Basso
Alan Remaley
Gyorgy Csako
Thomas L Eggerman
Amy P Patterson
National Heart Lung and Blood Institute · USCenter for Clinical Research (United States) · USNational Cancer Institute · MYNational Institute of Diabetes and Digestive and Kidney Diseases · USNational Institutes of Health · US

Funding

Performance Utility Of Tests For ArtherothrombosisZ01CL010306 · CLC · CLINICAL CENTER · PI CSAKO, GYORGY · 1999 to 2008
$55k
Analytical Performance/Clinical Utility Of Laboratory Tests For AtherothrombosisZIACL010306 · CLC · CLINICAL CENTER · PI CSAKO, GYORGY · 2009 to 2010
$0k
6 · The paper itself

Abstract

CD36 and LIMPII analog 1, CLA-1, and its splicing variant, CLA-2 (SR-BI and SR-BII in rodents), are human high density lipoprotein receptors with an identical extracellular domain which binds a spectrum of ligands including bacterial cell wall components. In this study, CLA-1- and CLA-2-stably transfected HeLa and HEK293 cells demonstrated several-fold increases in the uptake of various bacteria over mock-transfected cells. All bacteria tested, including both Gram-negatives (Escherichia coli K12, K1 and Salmonella typhimurium) and Gram-positives (Staphylococcus aureus and Listeria monocytogenes), demonstrated various degrees of lower uptake in control cells. This result is consistent with the presence of high-density lipoprotein-receptor-independent bacterial uptake that is enhanced by CLA-1/CLA-2 overexpression. Bacterial lipopolysaccharides, lipoteichoic acid, and synthetic amphipathic helical peptides (L-37pA and D-37pA) competed with E. coli K12 for CLA-1 and CLA-2 binding. Transmission electron microscopy and confocal microscopy revealed cytosolic accumulation of bacteria in CLA-1/CLA-2-overexpressing HeLa cells. The antibiotic protection assay confirmed that E. coli K12 was able to survive and replicate intracellularly in CLA-1- and CLA-2-overexpressing HeLa, but both L-37pA and D-37pA prevented E. coli K12 invasion. Peritoneal macrophages isolated from SR-BI/BII-knockout mice demonstrated a 30% decrease in bacterial uptake when compared with macrophages from normal mice. Knockout macrophages were also characterized by decreased bacterial cytosolic invasion, ubiquitination, and proteasome mobilization while retaining bacterial lysosomal accumulation. These results indicate that, by facilitating bacterial adhesion and cytosolic invasion, CLA-1 and CLA-2 may play an important role in infection and sepsis.

Indexed as

Alternative SplicingAnimalsBacterial AdhesionCD36 AntigensCell LineCytosolEscherichia coli K12HeLa CellsHumansIn Vitro TechniquesLysosomal Membrane ProteinsMacrophages, PeritonealMiceMice, Inbred C57BLMice, KnockoutMicroscopy, ElectronCD36 AntigensLysosomal Membrane ProteinsSCARB1 protein, humanScarb2 protein, mouseScavenger Receptors, Class B

Identifiers

PMID17071747
PMCPMC1636549
OpenAlexW2018557879

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.