Evidence map›Paper›PMID 18511572›Full record

ArticleJournal of leukocyte biology2008

Separate endocytic pathways regulate IL-5 receptor internalization and signaling.

Jonathan T Lei, Margarita Martinez-Moczygemba

Abstract read
In one paragraph

Article in Journal of leukocyte biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Transcription Factor Repertoire of Homeostatic Eosinophilopoiesis.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  7. Article
  8. Article
  9. Article
  10. Clathrin mediates endocytosis of progastrin and activates MAPKs: role of cell surface annexin A2.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Article
  11. Article
  12. Article
  13. Constitutive exposure of phosphatidylserine on viable cells.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  14. Article
  15. Review
  16. IL-5 receptor α levels in patients with marked eosinophilia or mastocytosis.The Journal of allergy and clinical immunology · 2011
    Article
  17. T-helper cell type 2 (Th2) memory T cell-potentiating cytokine IL-25 has the potential to promote angiogenesis in asthma.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  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

2 authors at 1 institution in 1 country.

Jonathan T LeiBiology of Inflammation Center, Baylor College of Medicine, Houston, TX 77030-3411, USA.
Margarita Martinez-Moczygemba
Baylor College of Medicine · US

Funding

Proteasome Regulation of Interleukin-5 Receptor EndocytosisR01AI063178 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI MARTINEZ-MOCZYGEMBA, MAGARITA · 2004 to 2007
$1.1M
NIAID NIH HHS AI 063178NIAID NIH HHS R01 AI063178
6 · The paper itself

Abstract

Eosinophils are critically dependent on IL-5 for their activation, differentiation, survival, and augmentation of cytotoxic activity. We previously showed that the cytoplasmic domain of the hematopoietic receptor, betac, which is shared by IL-5, IL-3, and GM-CSF, is directly ubiquitinated and degraded by the proteasomes in a JAK2-dependent manner. However, studies describing the spatial distribution, endocytic regulation, and trafficking of betac-sharing receptors in human eosinophils are currently lacking. Using deconvolution microscopy and biochemical methods, we clearly demonstrate that IL-5Rs reside in and are internalized by clathrin- and lipid raft-dependent endocytic pathways. Microscopy analyses in TF1 cells and human eosinophils revealed significant colocalization of betac, IL-5Ralpha, and Cy3-labeled IL-5 with transferrin- (clathrin) and cholera toxin-B- (lipid raft) positive vesicles. Moreover, whereas internalized IL-5Rs were detected in both clathrin- and lipid raft-positive vesicles, biochemical data revealed that tyrosine phosphorylated, ubiquitinated, and proteasome-degraded IL-5Rs partitioned to the soluble, nonraft fractions (clathrin-containing). Lastly, we show that optimal IL-5-induced signaling requires entry of activated IL-5Rs into the intracellular compartment, as coimmunoprecipitation of key signaling molecules with the IL-5R was completely blocked when either endocytic pathway was inhibited. These data provide the first evidence that IL-5Rs segregate and traffic into two distinct plasma membrane compartments, and they further establish that IL-5R endocytosis regulates signaling both positively and negatively.

Indexed as

Cell Line, TumorCell MembraneCholera ToxinClathrinEndocytosisEosinophilsFlow CytometryHumansInterleukin-5Leukemia, Erythroblastic, AcuteReceptors, Interleukin-5Signal TransductionTransferrinCholera ToxinClathrinInterleukin-5Receptors, Interleukin-5Transferrin

Identifiers

PMID18511572
PMCPMC2493073
OpenAlexW2107049304

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.