Evidence map›Paper›PMID 23820734›Full record

ArticleCell and tissue research2013

Intestinal stem cells remain viable after prolonged tissue storage.

Megan K Fuller, Denver M Faulk, Nambirajan Sundaram, Maxime M Mahe, Kara M Stout, Richard J von Furstenberg, Brian J Smith, Kirk K McNaughton, Noah F Shroyer, Michael A Helmrath and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cell and tissue research, 2013. 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
1.4field-weighted citation impact, top 19% 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, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Preservation of reserve intestinal epithelial stem cells following severe ischemic injury.American journal of physiology. Gastrointestinal and liver physiology · 2019
    Article
  8. Review
  9. Article
  10. A paradox of transcriptional and functional innate interferon responses of human intestinal enteroids to enteric virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  11. Review
  12. Article
  13. Article
  14. Animal models of ischemia-reperfusion-induced intestinal injury: progress and promise for translational research.American journal of physiology. Gastrointestinal and liver physiology · 2015
    Review
  15. Article
  16. Establishment of Gastrointestinal Epithelial Organoids.Current protocols in mouse biology · 2013
    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

11 authors at 2 institutions in 1 country.

Megan K FullerDepartment of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Denver M Faulk
Nambirajan Sundaram
Maxime M Mahe
Kara M Stout
Richard J von Furstenberg
Brian J Smith
Kirk K McNaughton
Noah F Shroyer
Michael A Helmrath
Susan J Henning
University of North Carolina at Chapel Hill · USCincinnati Children's Hospital Medical Center · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI David Darr · 1985 to 2026
$201.5M
PILOT AND FEASIBILITY STUDIESP30DK034987 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Temitope O. Keku · 1985 to 2026
$30.5M
Intestinal Stem Cell Consortium Coordinating CenterU01DK085532 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI NILAND, JOYCE CAROL · 2009 to 2018
$6.5M
Limited Competition for the Continuation of the Intestinal Stem Cell Consortium Coordinating CenterU24DK085532 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI NILAND, JOYCE CAROL · 2019 to 2023
$2.3M
Collaborative Approaches to the Study of Intestinal Epithelial Stem CellsU01DK085547 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HENNING, SUSAN J. · 2009 to 2013
$2.0M
KLF5 regulation of intestinal development and stem cell homeostasis.R01DK092306 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI SHROYER, NOAH FREEMAN · 2011 to 2014
$1.6M
Mechanisms of Intestinal Stem Cell Expansion Following ResectionR01DK083325 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HELMRATH, MICHAEL A. · 2009 to 2013
$1.5M
The role of ATOH1 as a tumor suppressor in colorectal cancerR01CA142826 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI SHROYER, NOAH FREEMAN · 2010 to 2014
$1.5M
NCI NIH HHS P30 CA016086NCI NIH HHS P30CA06086NCI NIH HHS R01 CA142826NIDDK NIH HHS P30 DK034987NIDDK NIH HHS R01 DK083325NIDDK NIH HHS R01-DK083325NIDDK NIH HHS R01 DK092306NIDDK NIH HHS U01 DK085532NIDDK NIH HHS U01 DK085547NIDDK NIH HHS U01-DK085547NIDDK NIH HHS U24 DK085532
6 · The paper itself

Abstract

Intestinal stem cells (ISCs) are responsible for renewal of the epithelium both during normal homeostasis and following injury. As such, they have significant therapeutic potential. However, whether ISCs can survive tissue storage is unknown. We hypothesize that, although the majority of epithelial cells might die, ISCs would remain viable for at least 24 h at 4 °C. To explore this hypothesis, jejuna of C57Bl6/J or Lgr5-LacZ mice were removed and either processed immediately or placed in phosphate-buffered saline at 4 °C. Delayed isolation of epithelium was performed after 24, 30, or 48 h storage. At the light microscope level, despite extensive apoptosis of villus epithelial cells, small intestinal crypts remained morphologically intact for 30 h and ISCs were identifiable via Lgr5-LacZ positivity. Electron microscopy showed that ISCs retained high integrity for 24 h. When assessed by flow cytometry, ISCs were more resistant to degeneration than the rest of the epithelium, including neighboring Paneth cells, with higher viability across all time points. Cultured isolated crypts showed no loss of capacity to form complex enteroids after 24 h tissue storage, with efficiencies after 7 days of culture remaining above 80 %. By 30 h storage, efficiencies declined but budding capability was retained. We conclude that, with delay in isolation, ISCs remain viable and retain their proliferative capacity. In contrast, the remainder of the epithelium, including the Paneth cells, exhibits degeneration and programmed cell death. If these findings are recapitulated in human tissue, storage at 4 °C might offer a valuable temporal window for the harvesting of crypts or ISCs for therapeutic application.

Indexed as

AnimalsApoptosisCell Culture TechniquesCell ProliferationCells, CulturedCell SeparationCell SurvivalHumansIntestinal MucosaJejunumMaleMiceMice, Inbred C57BLStem CellsTissue Preservation

Identifiers

PMID23820734
PMCPMC3812345
OpenAlexW1979408091

What OpenQuestion holds

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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.