Evidence map›Paper›PMID 15625104›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

Selective up-regulation of PDE1B2 upon monocyte-to-macrophage differentiation.

Andrew T Bender, Cari L Ostenson, Edith H Wang, Joseph A Beavo

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 19% 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, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. CaCell reports · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Cyclic nucleotide phosphodiesterase 1C contributes to abdominal aortic aneurysm.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. Sex-Steroid Signaling in Lung Diseases and Inflammation.Advances in experimental medicine and biology · 2021
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Foxm1 regulates resolution of hyperoxic lung injury in newborns.American journal of respiratory cell and molecular biology · 2015
    Article
  18. Article
  19. Multifunctional cationic peptide fractions from flaxseed protein hydrolysates.Plant foods for human nutrition (Dordrecht, Netherlands) · 2012
    Article
  20. 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

4 authors at 1 institution in 1 country.

Andrew T BenderDepartment of Pharmacology, University of Washington Medical School, Seattle, WA 98195-7280, USA.
Cari L Ostenson
Edith H Wang
Joseph A Beavo
University of Washington Medical Center · US

Funding

EXPERIMENTAL PATHOLOGY OF CARDIOVASCULAR DISEASET32HL007312 · NHLBI · UNIVERSITY OF WASHINGTON · PI MAJESKY, MARK W., SCHWARTZ, STEPHEN MARK · 1985 to 2019
$11.8M
METABOLISM AND FUNCTION OF CYCLIC NUCLEOTIDESR01DK021723 · NIDDK · UNIVERSITY OF WASHINGTON · PI BEAVO, JOSEPH A · 1986 to 2007
$2.9M
CHCR:A Protein in Mammalian Muscle DifferentiationR01AR049042 · NIAMS · UNIVERSITY OF WASHINGTON · PI WANG, EDITH HARRIET · 2003 to 2007
$1.2M
NHLBI NIH HHS HL-07312NHLBI NIH HHS T32 HL007312NIAMS NIH HHS ARO49042NIDDK NIH HHS DK21723NIDDK NIH HHS R01 DK021723
6 · The paper itself

Abstract

Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a major regulator of monocyte to macrophage differentiation. In both humans and mice, the main phenotype of decreased GM-CSF function is pulmonary proteinosis due to aberrant function of alveolar macrophages. Recently, this cytokine has been shown to up-regulate a cyclic nucleotide phosphodiesterase, PDE1B. Two PDE1B variants with unique N-terminal sequences, PDE1B1 and PDE1B2, have been identified. Here, we report that the previously uncharacterized PDE1B2 is selectively increased by GM-CSF by stimulation of transcription at a previously unknown transcriptional start site. Analysis of the exon and intron organization of the PDE1B gene reveals that PDE1B2 has a different N-terminal sequence because of a separate first exon that is located 11.5 kb downstream from the PDE1B1 first exon. By using 5'-RACE, alignment of EST sequences, and a luciferase-reporter system, we provide evidence that PDE1B2 has a separate transcriptional start site from PDE1B1 that can be activated by monocyte differentiation. Furthermore, IL-4 treatment in the presence of GM-CSF, which shifts the differentiation from a macrophage to a dendritic cell phenotype, suppresses the up-regulation of PDE1B2. Induction of PDE1B2 is also found in T cells upon activation by PHA. Therefore, PDE1B2 may have a regulatory role in multiple immune cell types. Last, characterization of the catalytic properties of recombinant PDE1B2 shows that it prefers cGMP over cAMP as a substrate and, thus, is likely to regulate cGMP in macrophages. Also, PDE1B2 has a nearly 3-fold lower EC(50) for activation by calmodulin than PDE1B1.

Indexed as

Cell DifferentiationCells, CulturedCyclic Nucleotide Phosphodiesterases, Type 1Dendritic CellsHumansInterleukin-4KineticsMacrophagesMonocytesPhosphoric Diester HydrolasesPromoter Regions, GeneticRNA, MessengerTranscription Initiation SiteUp-RegulationCyclic Nucleotide Phosphodiesterases, Type 1Interleukin-4PDE1B protein, humanPhosphoric Diester HydrolasesRNA, Messenger

Identifiers

PMID15625104
PMCPMC544304
OpenAlexW2054663379

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.