Evidence map›Paper›PMID 18997827›Full record

ArticleBone marrow transplantation2009

Haematopoietic repopulating activity in human cord blood CD133+ quiescent cells.

S A Boxall, G P Cook, D Pearce, D Bonnet, Y M El-Sherbiny, M P Blundell, S J Howe, J P Leek, A F Markham, E A de Wynter

Abstract read
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In one paragraph

Article in Bone marrow transplantation, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 22 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

S A BoxallDepartment of Molecular Gastroenterology, Leeds Institute of Molecular Medicine, University of Leeds, Leeds, UK.
G P Cook
D Pearce
D Bonnet
Y M El-Sherbiny
M P Blundell
S J Howe
J P Leek
A F Markham
E A de Wynter
University of Leeds · GBCancer Research UK · GBUniversity College London · GB

Funding

Cancer Research UK
6 · The paper itself

Abstract

We have demonstrated previously that cord blood CD133(+) cells isolated in the G(0) phase of the cell cycle are highly enriched for haematopoietic stem cell (HSC) activity, in contrast to CD133(+)G(1) cells. Here, we have analysed the phenotype and functional properties of this population in more detail. Our data demonstrate that a large proportion of the CD133(+)G(0) cells are CD38 negative (60.4%) and have high aldehyde dehydrogenase activity (75.1%) when compared with their CD133(+)G(1) counterparts (13.5 and 4.1%, respectively). This suggests that stem cell activity resides in the CD133(+)G(0) population. In long-term BM cultures, the CD133(+)G(0) cells generate significantly more progenitors than the CD34(+)G(0) population (P<0.001) throughout the culture period. Furthermore, a comparison of CD133(+)G(0) versus CD133(+)G(1) cells revealed that multilineage reconstitution was obtained only in non-obese diabetic/SCID animals receiving G(0) cells. We conclude that CD133(+) cells in the quiescent phase of the cell cycle have a phenotype consistent with HSCs and are highly enriched for repopulating activity when compared with their G(1) counterparts. This cell population should prove useful for selection and manipulation in ex vivo expansion protocols.

Indexed as

AC133 AntigenAldehyde DehydrogenaseAnimalsAntigens, CDAntigens, CD34Bone Marrow CellsCell Culture TechniquesCell CycleFetal BloodGlycoproteinsHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHumansMiceMice, Inbred NODMice, SCIDAC133 AntigenAldehyde DehydrogenaseAntigens, CDAntigens, CD34GlycoproteinsPeptidesPROM1 protein, humanProm1 protein, mouse

Identifiers

PMID18997827
OpenAlexW1981835049

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.