Evidence map›Paper›PMID 18511597›Full record

ArticleStem cells (Dayton, Ohio)2008

Diverse adult stem cells share specific higher-order patterns of gene expression.

Jason M Doherty, Michael J Geske, Thaddeus S Stappenbeck, Jason C Mills

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 30 citations in OpenAlex.

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  9. MIST1-a novel marker of plasmacytic differentiation.Applied immunohistochemistry & molecular morphology : AIMM · 2012
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  11. Sorting mouse jejunal epithelial cells with CD24 yields a population with characteristics of intestinal stem cells.American journal of physiology. Gastrointestinal and liver physiology · 2011
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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

4 authors at 1 institution in 1 country.

Jason M DohertyDepartment of Pathology and Immunology, Washington University School of Medicine, Box 8118, 660 South Euclid Avenue, St. Louis, Missouri 63110, USA.
Michael J Geske
Thaddeus S Stappenbeck
Jason C Mills
Washington University in St. Louis · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
Pancreas Transcription Factors and Disease Model SystemsR01DK055489 · NIDDK · PURDUE UNIVERSITY WEST LAFAYETTE · PI KONIECZNY, STEPHEN F · 2000 to 2017
$5.6M
MOLECULAR REGULATION OF GASTRIC CHIEF (ZYMOGENIC) CELL DIFFERENTIATIONR01DK079798 · NIDDK · WASHINGTON UNIVERSITY · PI MILLS, JASON C · 2008 to 2012
$1.6M
Molecular regulation of gastric epithelial renewalK08DK066062 · NIDDK · WASHINGTON UNIVERSITY · PI MILLS, JASON C · 2004 to 2008
$598k
Responses of Intestinal Stem Cells to Epithelial InjuryR03DK066220 · NIDDK · WASHINGTON UNIVERSITY · PI STAPPENBECK, THADDEUS S · 2004 to 2005
$153k
NCI NIH HHS P30 CA091842NCI NIH HHS P30-CA91842NIDDK NIH HHS K08 DK066062NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30-DK52574NIDDK NIH HHS R01 DK055489NIDDK NIH HHS R01 DK079798NIDDK NIH HHS R01-DK079798NIDDK NIH HHS R03 DK066220NIDDK NIH HHS R03-DK55489
6 · The paper itself

Abstract

Adult tissue stem cells (SCs) share functional properties regardless of their tissue of residence. It had been thought that SCs might also share expression of certain "stemness" genes, although early investigations for such genes were unsuccessful. Here, we show that SCs from diverse tissues do preferentially express certain types of genes and that SCs resemble other SCs in terms of global gene expression more than they resemble the differentiated cells (DCs) of the tissues that they supply. Genes associated with nuclear function and RNA binding were over-represented in SCs. In contrast, DCs from diverse tissues shared enrichment in genes associated with extracellular space, signal transduction, and the plasma membrane. Further analysis showed that transit-amplifying cells could be distinguished from both SCs and DCs by heightened expression of cell division and DNA repair genes and decreased expression of apoptosis-related genes. This transit-amplifying cell-specific signature was confirmed by de novo generation of a global expression profile of a cell population highly enriched for transit-amplifying cells: colonic crypt-base columnar cells responding to mucosal injury. Thus, progenitor cells preferentially express intracellular or biosynthetic genes, and differentiation correlates with increased expression of genes for interacting with other cells or the microenvironment. The higher-order, Gene Ontology term-based analysis we use to distinguish SC- and DC-associated gene expression patterns can also be used to identify intermediate differentiation states (e.g., that of transit-amplifying cells) and, potentially, any biological state that is reflected in changes in global gene expression patterns. Disclosure of potential conflicts of interest is found at the end of this article.

Indexed as

Gene Expression ProfilingAdult Stem CellsAlgorithmsAnimalsCell DifferentiationCell DivisionCell MembraneDNADNA RepairGene Expression RegulationHumansMiceMice, Inbred C57BLRNASignal TransductionDNARNA

Identifiers

PMID18511597
PMCPMC2610416
OpenAlexW2086801645

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.