Evidence map›Paper›PMID 12782718›Full record

ArticleThe Journal of experimental medicine2003

Marrow stem cells shift gene expression and engraftment phenotype with cell cycle transit.

Jean-Francois Lambert, Meng Liu, Gerald A Colvin, Mark Dooner, Christina I McAuliffe, Pamela S Becker, Bernard G Forget, Sherman M Weissman, Peter J Quesenberry

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 81 citations in OpenAlex.

  1. Trial
  2. The Essence of Quiescence.Stem cells and development · 2024
    Review
  3. The universal stem cell.Leukemia · 2022
    Review
  4. Article
  5. Review
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  14. Review
  15. Article
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  17. Article
  18. Murine allogeneic in vivo stem cell homing(,).Journal of cellular physiology · 2007
    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

9 authors at 5 institutions in 2 countries.

Jean-Francois LambertDepartment of Research, Roger Williams Medical Center, 825 Chalkstone Ave., Providence, RI 02908, USA.
Meng Liu
Gerald A Colvin
Mark Dooner
Christina I McAuliffe
Pamela S Becker
Bernard G Forget
Sherman M Weissman
Peter J Quesenberry
Providence College · USYale University · USRoger Williams Medical Center · USSmith-Kettlewell Eye Research Institute · USUniversity of Massachusetts Chan Medical School · US

Funding

TRANSCRIPTIONAL REGULATION IN STEM CELLSP01HL056920 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI QUESENBERRY, PETER J · 1996 to 2000
$1.2M
STEM CELLS HOMING AND MOTILITYR01DK027424 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI QUESENBERRY, PETER J · 1986 to 2002
$927k
NHLBI NIH HHS P0-1 HL56920NIDDK NIH HHS P0-1 DK27424NIDDK NIH HHS R01 DK027424
6 · The paper itself

Abstract

We studied the genetic and engraftment phenotype of highly purified murine hematopoietic stem cells (lineage negative, rhodamine-low, Hoechst-low) through cytokine-stimulated cell cycle. Cells were cultured in interleukin (IL)-3, IL-6, IL-11, and steel factor for 0 to 48 h and tested for engraftment capacity in a lethally irradiated murine competitive transplant model. Engraftment showed major fluctuations with nadirs at 36 and 48 h of culture and recovery during the next G1. Gene expression of quiescent (0 h) or cycling (48 h) stem cells was compared with lineage positive cells by 3' end PCR differential display analysis. Individual PCR bands were quantified using a 0 to 9 scale and results were visually compared using color-coded matrices. We defined a set of 637 transcripts expressed in stem cells and not expressed in lineage positive cells. Gene expression analyzed at 0 and 48 h showed a major shift from "stem cell genes" being highly expressed at 0 h and turned off at 48 h, while "cell division" genes were turned on at 48 h. These observations suggest stem cell gene expression shifts through cell cycle in relation to cell cycle related alterations of stem cell phenotype. The engraftment defect is related to a major phenotypic change of the stem cell.

Indexed as

Hematopoietic Stem Cell TransplantationAnimalsBase SequenceCell CycleDNA, ComplementaryFemaleGene ExpressionGene Expression ProfilingHematopoietic Stem CellsInterleukin-11Interleukin-3Interleukin-6KineticsMiceMice, Inbred BALB CPhenotypeDNA, ComplementaryInterleukin-11Interleukin-3Interleukin-6Stem Cell Factor

Identifiers

PMID12782718
PMCPMC2193900
OpenAlexW2111228323

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.