Evidence map›Paper›PMID 20430777›Full record

ArticleJournal of leukocyte biology2010

CD13 is dispensable for normal hematopoiesis and myeloid cell functions in the mouse.

Beata Winnicka, Catherine O'Conor, Wolfgang Schacke, Kaitlyn Vernier, Christina L Grant, Fiona Hall Fenteany, Flavia E Pereira, Brannen Liang, Anupinder Kaur, Ran Zhao and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

27 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Coronavirus Receptors as Immune Modulators.Journal of immunology (Baltimore, Md. : 1950) · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Angiogenic and Arthritogenic Properties of the Soluble Form of CD13.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. CD13 mediates phagocytosis in human monocytic cells.Journal of leukocyte biology · 2015
    Article
  18. CD13 restricts TLR4 endocytic signal transduction in inflammation.Journal of immunology (Baltimore, Md. : 1950) · 2015
    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

14 authors at 1 institution in 1 country.

Beata WinnickaCenter for Vascular Biology, Department of Immunology, University of Connecticut Health Center, 263 Farmington Ave., Farmington, CT 06030-3501, USA.
Catherine O'Conor
Wolfgang Schacke
Kaitlyn Vernier
Christina L Grant
Fiona Hall Fenteany
Flavia E Pereira
Brannen Liang
Anupinder Kaur
Ran Zhao
David C Montrose
Daniel W Rosenberg
Hector L Aguila
Linda H Shapiro
UConn Health · US

Funding

CD13 as a Biomarker for NSAIDS Chemoprevention of Breast CancerR01CA106345 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI SHAPIRO, LINDA H · 2005 to 2009
$1.4M
NCI NIH HHS CA-106345
6 · The paper itself

Abstract

The robust and consistent expression of the CD13 cell surface marker on very early as well as differentiated myeloid hematopoietic cells has prompted numerous investigations seeking to define roles for CD13 in myeloid cells. To address the function of myeloid CD13 directly, we created a CD13 null mouse and assessed the responses of purified primary macrophages or DCs from WT and CD13 null animals in cell assays and inflammatory disease models, where CD13 has been implicated previously. We find that mice lacking CD13 develop normally with normal hematopoietic profiles except for an increase in thymic but not peripheral T cell numbers. Moreover, in in vitro assays, CD13 appears to be largely dispensable for the aspects of phagocytosis, proliferation, and antigen presentation that we tested, although we observed a slight decrease in actin-independent erythrocyte uptake. However, in agreement with our published studies, we show that lack of monocytic CD13 completely ablates anti-CD13-dependent monocyte adhesion to WT endothelial cells. In vivo assessment of four inflammatory disease models showed that lack of CD13 has little effect on disease onset or progression. Nominal alterations in gene expression levels between CD13 WT and null macrophages argue against compensatory mechanisms. Therefore, although CD13 is highly expressed on myeloid cells and is a reliable marker of the myeloid lineage of normal and leukemic cells, it is not a critical regulator of hematopoietic development, hemostasis, or myeloid cell function.

Indexed as

AnimalsCD13 AntigensDendritic CellsGene Expression RegulationHematopoiesisHematopoietic Stem CellsInflammationMacrophagesMiceMice, KnockoutMyeloid CellsCD13 Antigens

Identifiers

PMID20430777
PMCPMC2908940
OpenAlexW2099618132

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.