Evidence map›Paper›PMID 17016561›Full record

ArticleThe Journal of clinical investigation2006

Hematopoietic stem cells proliferate until after birth and show a reversible phase-specific engraftment defect.

Michelle B Bowie, Kristen D McKnight, David G Kent, Lindsay McCaffrey, Pamela A Hoodless, Connie J Eaves

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 207 papers.

0numbers the graph read from it
0cells of the map it votes in
207citing papers in PubMed
–field-weighted citation impact
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

207 citing papers in PubMed.

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147 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Michelle B BowieTerry Fox Laboratory, BC Cancer Agency, Vancouver, British Columbia, Canada.
Kristen D McKnight
David G Kent
Lindsay McCaffrey
Pamela A Hoodless
Connie J Eaves

Funding

STEM CELLS AND GENE THERAPY MODELSP01HL055435 · NHLBI · YESHIVA UNIVERSITY · PI NAGEL, RONALD L · 1995 to 2004
$11.0M
NHLBI NIH HHS P01 HL055435NHLBI NIH HHS P01 HL-55435
6 · The paper itself

Abstract

The regulation of HSC proliferation and engraftment of the BM is an important but poorly understood process, particularly during ontogeny. Here we show that in mice, all HSCs are cycling until 3 weeks after birth. Then, within 1 week, most became quiescent. Prior to 4 weeks of age, the proliferating HSCs with long-term multilineage repopulating activity displayed an engraftment defect when transiting S/G2/M. During these cell cycle phases, their expression of CXC chemokine ligand 12 (CXCL12; also referred to as stromal cell-derived factor 1 [SDF-1]) transiently increased. The defective engrafting activity of HSCs in S/G2/M was reversed when cells were allowed to progress into G1 prior to injection or when the hosts (but not the cells) were pretreated with a CXCL12 antagonist. Interestingly, the enhancing effect of CXCL12 antagonist pretreatment was exclusive to transplants of long-term multilineage repopulating HSCs in S/G2/M. These results demonstrate what we believe to be a new HSC regulatory checkpoint during development. They also suggest an ability of HSCs to express CXCL12 in a fashion that changes with cell cycle progression and is associated with a defective engraftment that can be overcome by in vivo administration of a CXCL12 antagonist.

Indexed as

Cell ProliferationAnimalsAnimals, NewbornBone Marrow CellsCell CycleChemokine CXCL12Chemokines, CXCFluorouracilGene ExpressionGraft SurvivalHematopoiesisHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHematopoietic SystemHyaluronan ReceptorsIntegrin alpha4Chemokine CXCL12Chemokines, CXCCxcl12 protein, mouseFluorouracilHyaluronan ReceptorsIntegrin alpha4Proto-Oncogene Proteins c-kitReceptors, CXCR4ThymidineVascular Cell Adhesion Molecule-1

Identifiers

PMID17016561
PMCPMC1578623

What OpenQuestion holds

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Registered trials

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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.