Evidence map›Paper›PMID 9077547›Full record

ArticleThe Journal of clinical investigation1997

Crypt stem cell survival in the mouse intestinal epithelium is regulated by prostaglandins synthesized through cyclooxygenase-1.

S M Cohn, S Schloemann, T Tessner, K Seibert, W F Stenson

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
12.0field-weighted citation impact, top 1% 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

65 citing papers in PubMed, 223 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. COX-1/PGEScientific reports · 2017
    Article
  19. The whipworm (Trichuris suis) secretes prostaglandin E2 to suppress proinflammatory properties in human dendritic cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  20. Review

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

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

5 authors at 2 institutions in 1 country.

S M CohnDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
S Schloemann
T Tessner
K Seibert
W F Stenson
Washington University in St. Louis · USPfizer (United States) · US

Funding

MEDIATORS OF INFLAMMATION IN INFLAMMATORY BOWEL DISEASER01DK033165 · NIDDK · WASHINGTON UNIVERSITY · PI STENSON, WILLIAM F. · 1986 to 2006
$1.9M
FIBROBLAST GROWTH FACTORS IN INFLAMMATORY BOWEL DISEASER01DK050924 · NIDDK · WASHINGTON UNIVERSITY · PI COHN, STEVEN M · 1995 to 2002
$785k
INJURY REPAIR AND GROWTH FACTORS IN GUT DEVELOPMENTR01HD031914 · NICHD · WASHINGTON UNIVERSITY · PI COHN, STEVEN M · 1994 to 1996
–
NICHD NIH HHS R01 HD-31914NIDDK NIH HHS R01 DK-33165NIDDK NIH HHS R01 DK-50924
6 · The paper itself

Abstract

Prostaglandins (PGs) are important mediators of epithelial integrity and function in the gastrointestinal tract. Relatively little is known, however, about the mechanism by which PGs affect stem cells in the intestine during normal epithelial turnover, or during wound repair. PGs are synthesized from arachidonate by either of two cyclooxygenases, cyclooxygenase-1 (Cox-1) or cyclooxygenase-2 (Cox-2), which are present in a wide variety of mamalian cells. Cox-1 is thought to be a constitutively expressed enzyme, and the expression of Cox-2 is inducible by cytokines or other stimuli in a variety of cell types. We investigated the role of PGs in mouse intestinal stem cell survival and proliferation following radiation injury. The number of surviving crypt stem cells was determined 3.5 d after irradiation by the microcolony assay. Radiation injury induced a dose-dependent decrease in the number of surviving crypts. Indomethacin, an inhibitor of Cox-1 and Cox-2, further reduced the number of surviving crypts in irradiated mice. The indomethacin dose response for inhibition of PGE2 production and reduction of crypt survival were similar. DimethylPGE2 reversed the indomethacin-induced decrease in crypt survival. Selective Cox-2 inhibitors had no effect on crypt survival. PGE2, Cox-1 mRNA, and Cox-1 protein levels all increase in the 3 d after irradiation. Immunohistochemistry for Cox-1 demonstrated localization in epithelial cells of the crypt in the unirradiated mouse, and in the regenerating crypt epithelium in the irradiated mouse. We conclude that radiation injury results in increased Cox-1 levels in crypt stem cells and their progeny, and that PGE2 produced through Cox-1 promotes crypt stem cell survival and proliferation.

Indexed as

AnimalsCell SurvivalCyclooxygenase 1DinoprostoneEpithelial CellsEpitheliumFemaleGamma RaysIndomethacinIntestinal MucosaIsoenzymesMembrane ProteinsMiceMice, Inbred StrainsProstaglandin AntagonistsProstaglandin-Endoperoxide SynthasesCyclooxygenase 1DinoprostoneIndomethacinIsoenzymesMembrane ProteinsProstaglandin AntagonistsProstaglandin-Endoperoxide SynthasesPtgs1 protein, mouseRNA, Messenger

Identifiers

PMID9077547
PMCPMC507953
OpenAlexW2060571271

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.