Evidence map›Paper›PMID 22855602›Full record

ArticleBlood2012

Myeloid skewing in murine autoimmune arthritis occurs in hematopoietic stem and primitive progenitor cells.

Kwadwo A Oduro, Fang Liu, Qing Tan, Chan-Kyu Kim, Olga Lubman, Daved Fremont, Jason C Mills, Kyunghee Choi

Open access · greenAbstract read
In one paragraph

Article in Blood, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.5field-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

41 citing papers in PubMed, 64 citations in OpenAlex.

  1. Trial
  2. Aryl hydrocarbon receptor activation alters emergency hematopoiesis during influenza A virus infection.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Extramedullary hematopoiesis in cancer.Experimental & molecular medicine · 2024
    Review
  9. DNA hypomethylation ameliorates erosive inflammatory arthritis by modulating interferon regulatory factor-8.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Impact ofFrontiers in immunology · 2024
    Article
  11. Article
  12. Innate immune memory in inflammatory arthritis.Nature reviews. Rheumatology · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
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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

8 authors at 2 institutions in 2 countries.

Kwadwo A OduroDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63110, USA.
Fang Liu
Qing Tan
Chan-Kyu Kim
Olga Lubman
Daved Fremont
Jason C Mills
Kyunghee Choi
Institute for Stem Cell Biology and Regenerative Medicine · INWashington University in St. Louis · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Hemangioglast Development and RegulationR01HL055337 · NHLBI · WASHINGTON UNIVERSITY · PI CHOI, KYUNGHEE · 2001 to 2024
$9.1M
HEMATOPOIETIC COMMITMENT: MOLECULAR MECHANISMSR01HL063736 · NHLBI · WASHINGTON UNIVERSITY · PI CHOI, KYUNGHEE · 2000 to 2016
$5.6M
HEMANGIOBLAST DEVELOPMENT AND REGULATIONR29HL055337 · NHLBI · WASHINGTON UNIVERSITY · PI CHOI, KYUNGHEE · 1996 to 2000
$94k
NCI NIH HHS P30 CA091842NCI NIH HHS P30 CA91842NHLBI NIH HHS HL55337NHLBI NIH HHS HL63736NHLBI NIH HHS R01 HL055337NHLBI NIH HHS R01 HL063736NHLBI NIH HHS R29 HL055337
6 · The paper itself

Abstract

Skewing toward myeloid cell production is often observed in chronic inflammation and autoimmune diseases. Herein, we determined whether persistent myeloid activation and proinflammatory output occurring in pathologic conditions is at the level of hematopoietic stem and primitive progenitor cells (HSPPCs). By using a mouse arthritis model, we found that even though HSPPCs in arthritis still retained the capacity to differentiate into different lineages, they acquired enhanced in vitro and in vivo propensity in a disease-dependent manner to generate myeloid cells, the key perpetrators of tissue damage in arthritis. This myeloid skewing was cell intrinsic, as arthritic HSPPCs up-regulate myeloid-specific transcripts including S100a8. Exogenous S100a8 promoted myeloid cell output from wild-type HSPPCs, suggesting mechanistic involvement of this gene in the myeloid priming that occurs in arthritic HSPPCs. Therefore, our results indicate that in arthritic mice, HSPPCs adopt a pathologic state that favors disease persistence.

Indexed as

Disease Models, AnimalMyelopoiesisAnimalsArthritis, RheumatoidCalgranulin ACells, CulturedGene Expression ProfilingHematopoietic Stem CellsLymphopoiesisMiceMice, CongenicMice, Inbred StrainsMice, TransgenicMyeloid Progenitor CellsOligonucleotide Array Sequence AnalysisRNA, MessengerCalgranulin ARNA, MessengerS100a8 protein, mouse

Identifiers

PMID22855602
PMCPMC3447779
OpenAlexW2012376370

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.