Evidence map›Paper›PMID 21155807›Full record

ArticleJournal of neurochemistry2011

Rapid endocytosis of interleukin-15 by cerebral endothelia.

Kirsten P Stone, Abba J Kastin, Hung Hsuchou, Chuanhui Yu, Weihong Pan

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of neurochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. NFĸB is an unexpected major mediator of interleukin-15 signaling in cerebral endothelia.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2011
    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

5 authors at 1 institution in 1 country.

Kirsten P StoneBlood-Brain Barrier Group, Pennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Abba J Kastin
Hung Hsuchou
Chuanhui Yu
Weihong Pan
Pennington Biomedical Research Center · US

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2005 to 2026
$26.5M
Neuroimmune modulation across the BBB: Regulation of ILS trafficking by TNFR01NS062291 · NINDS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI PAN, WEIHONG · 2008 to 2012
$1.6M
Anthropometric Assessment of Abdominal Obesity and Health Risk in Children and AdRC1DK086881 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI KATZMARZYK, PETER TODD · 2009 to 2010
$997k
Leptin Transport across the BBB: The Role of ObR (+) astrocytesR56DK054880 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI KASTIN, ABBA J · 2010 to 2010
$222k
NIDDK NIH HHS DK86881NIDDK NIH HHS P30 DK072476NIDDK NIH HHS R56 DK054880NIDDK NIH HHS RC1 DK086881NINDS NIH HHS NS62291NINDS NIH HHS R01 NS062291
6 · The paper itself

Abstract

Interleukin (IL)-15 receptors are present in the cerebral endothelia composing the blood-brain barrier where they show robust up-regulation by neuroinflammation. To determine how IL15 receptor subunits participate in the endocytosis and intracellular trafficking of IL15, we performed confocal microscopic imaging and radioactive tracer uptake assays in primary brain microvessel endothelial cells and related cell lines transfected with modulatory molecules. By immunostaining and co-localization studies with organelle markers, we showed that IL15 was rapidly endocytosed via lipid rafts and was directed to diverse intracellular pathways. During the course of intracellular trafficking, Alexa dye-conjugated IL15 was partially co-localized with both the specific receptor IL15Rα and the co-receptor IL2Rγ. However, deletion of one of the receptor subunits had only a minor effect in slowing IL15 uptake when primary brain microvessel endothelial cells from the receptor knockout mice were compared with those from wildtype mice. IL15 was trafficked to early, recycling, and late endosomes, to the Golgi, and to lysosomes. The diffuse distribution suggests that IL15 activates multiple endothelial signaling events.

Indexed as

AnimalsBlood-Brain BarrierCell CycleCell LineCells, CulturedCerebral CortexEndocytosisEndothelium, VascularHumansInflammation MediatorsInterleukin-15Interleukin Receptor Common gamma SubunitMiceMice, Inbred C57BLMice, KnockoutProtein TransportIl15ra protein, mouseInflammation MediatorsInterleukin-15Interleukin Receptor Common gamma SubunitReceptors, Interleukin-15

Identifiers

PMID21155807
PMCPMC3076997
OpenAlexW1485670558

What OpenQuestion holds

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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.