Evidence map›Paper›PMID 18665337›Full record

ReviewStem cell reviews2008

The paradoxical dynamism of marrow stem cells: considerations of stem cells, niches, and microvesicles.

Peter J Quesenberry, Jason M Aliotta

Abstract readReview
In one paragraph

Review in Stem cell reviews, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Trial
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  6. Extracellular Vesicles in the Development of Cancer Therapeutics.International journal of molecular sciences · 2020
    Review
  7. Article
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  19. Circulating miRNAs as biomarkers for endocrine disorders.Journal of endocrinological investigation · 2016
    Review
  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

2 authors.

Peter J QuesenberryDepartment of Medicine, The Warren Alpert Medical School of Brown University, Providence, RI, USA. pquesenberry@lifespan.org
Jason M Aliotta

Funding

WATER CHANNEL AQUAPORIN-3 IN BM-DERIVED EPIDERMAL CELLS PLAY ROLE WOUND HEALINGP20RR018757 · NCRR · ROGER WILLIAMS HOSPITAL · PI COUSENS, LESLIE P · 2003 to 2011
$22.5M
Cell Cycle Related Transdifferentiation into Lung CellsR01HL073749 · NHLBI · ROGER WILLIAMS HOSPITAL · PI QUESENBERRY, PETER J · 2003 to 2006
$1.8M
Minimal Treatment Models of Stem Cell EngraftmentR01DK061858 · NIDDK · ROGER WILLIAMS HOSPITAL · PI QUESENBERRY, PETER J · 2001 to 2004
$1.7M
Genetic information transfer to hematopoietic cells: Role of microvesiclesR01HL103726 · NHLBI · RHODE ISLAND HOSPITAL · PI QUESENBERRY, PETER J. · 2011 to 2014
$1.5M
Injured Lung and its Influence on Bone Marrow Cell PhenotypeK08HL086868 · NHLBI · RHODE ISLAND HOSPITAL · PI ALIOTTA, JASON M · 2008 to 2012
$634k
NCRR NIH HHS P20 RR018757NCRR NIH HHS P20RR018757NHLBI NIH HHS K08 HL086868NHLBI NIH HHS K08HL086868NHLBI NIH HHS R01 HL073749NHLBI NIH HHS R01HL073749NHLBI NIH HHS R01 HL103726NIDDK NIH HHS R01 DK061858NIDDK NIH HHS R01DK061858
6 · The paper itself

Abstract

Marrow stem cell regulation represents a complex and flexible system. It has been assumed that the system was intrinsically hierarchical in nature, but recent data has indicated that at the progenitor/stem cell level the system may represent a continuum with reversible alterations in phenotype occurring as the stem cells transit cell cycle. Short and long-term engraftment, in vivo and in vitro differentiation, gene expression, and progenitor numbers have all been found to vary reversibly with cell cycle. In essence, the stem cells appear to show variable potential, probably based on transcription factor access, as they proceed through cell cycle. Another critical component of the stem cell regulation is the microenvironment, so-called niches. We propose that there are not just several unique niche cells, but a wide variety of niche cells which continually change phenotype to appropriately interact with the continuum of stem cell phenotypes. A third component of the regulatory system is microvesicle transfer of genetic information between cells. We have shown that marrow cells can express the genetic phenotype of pulmonary epithelial cells after microvesicle transfer from lung to marrow cells. Similar transfers of tissue specific mRNA occur between liver, brain, and heart to marrow cells. Thus, there would appear to be a continuous genetic modulation of cells through microvesicle transfer between cells. We propose that there is an interactive triangulated Venn diagram with continuously changing stem cells interacting with continuously changing areas of influence, both being modulated by transfer of genetic information by microvesicles.

Indexed as

AnimalsBone Marrow CellsCell CommunicationCell CycleHumansMesenchymal Stem CellsModels, BiologicalReverse Transcriptase Polymerase Chain ReactionRNA, MessengerRNA, Messenger

Identifiers

PMID18665337
PMCPMC4495665

What OpenQuestion holds

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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.