Evidence map›Paper›PMID 18483182›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2008

Modulation of mouse intestinal epithelial cell turnover in the absence of angiotensin converting enzyme.

Emir Q Haxhija, Hua Yang, Ariel U Spencer, Hiroyuki Koga, Xiaoyi Sun, Daniel H Teitelbaum

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Special Issue "Zebrafish: A Model Organism for Human Health and Disease".International journal of molecular sciences · 2025
    Article
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  3. International journal of molecular sciences · 2024
    Article
  4. Article
  5. Review
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  7. Article
  8. Article
  9. Recent advances in small bowel diseases: Part II.World journal of gastroenterology · 2012
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

6 authors at 1 institution in 1 country.

Emir Q HaxhijaSection of Pediatric Surgery, Department of Surgery, University of Michigan Medical School, Ann Arbor, MI, USA.
Hua Yang
Ariel U Spencer
Hiroyuki Koga
Xiaoyi Sun
Daniel H Teitelbaum
University of Michigan–Ann Arbor · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
TPN INDUCED CHANGES IN INTRAEPITHELIAL LYMPHOCYTESR01AI044076 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TEITELBAUM, DANIEL H · 2004 to 2014
$3.2M
UNIVERSITY OF MICHIGAN MULTIPURPOSE ARTHRITIS CENTERP60AR020557 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SOWERS, MARYFRAN R · 1986 to 2001
$2.9M
TPN INDUCED CHANGES IN INTRAEPITHELIAL LYMPHOCYTESR29AI044076 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TEITELBAUM, DANIEL H · 1999 to 2003
$422k
NCI NIH HHS 5 P30 CA-46592NIAID NIH HHS AI44076-09NIAID NIH HHS R01 AI044076NIAMS NIH HHS AR-20557
6 · The paper itself

Abstract

Angiotensin converting enzyme (ACE) has been shown to be involved in regulation of apoptosis in nonintestinal tissues. This study examined the role of ACE in the modulation of intestinal adaptation utilizing ACE knockout mice (ACE-/-). A 60% small bowel resection (SBR) was used, since this model results in a significant increase in intestinal epithelial cell (EC) apoptosis as well as proliferation. Baseline villus height, crypt depth, and intestinal EC proliferation were higher, and EC apoptosis rates were lower in ACE-/- compared with ACE+/+ mice. After SBR, EC apoptosis rates remained significantly lower in ACE-/- compared with ACE+/+ mice. Furthermore, villus height and crypt depth after SBR continued to be higher in ACE-/- mice. The finding of a lower bax-to-bcl-2 protein ratio in ACE-/- mice may account for reduced EC apoptotic rates after SBR in ACE-/- compared with ACE+/+ mice. The baseline higher rate of EC proliferation in ACE-/- compared with ACE+/+ mice may be due to an increase in the expression of several EC growth factor receptors. In conclusion, ACE appears to have an important role in the modulation of intestinal EC apoptosis and proliferation and suggests that the presence of ACE in the intestinal epithelium has a critical role in guiding epithelial cell adaptive response.

Indexed as

AnimalsApoptosisCell ProliferationEpithelial CellsGene Expression RegulationIleumIntestinal MucosaJejunumMiceMice, Inbred C57BLMice, KnockoutMicroscopy, Electron, TransmissionPeptidyl-Dipeptidase APeptidyl-Dipeptidase A

Identifiers

PMID18483182
PMCPMC2494725
OpenAlexW2167904177

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.