Evidence map›Paper›PMID 26283731›Full record

ArticleMolecular and cellular biology2015

Loss of ADAM17-Mediated Tumor Necrosis Factor Alpha Signaling in Intestinal Cells Attenuates Mucosal Atrophy in a Mouse Model of Parenteral Nutrition.

Yongjia Feng, Yu-Hwai Tsai, Weidong Xiao, Matthew W Ralls, Alex Stoeck, Carole L Wilson, Elaine W Raines, Daniel H Teitelbaum, Peter J Dempsey

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2015. 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
3.2field-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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Myeloid ADAM17 induces ST2Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2025
    Article
  3. Review
  4. Fn14 and TNFR2 as regulators of cytotoxic TNFR1 signaling.Frontiers in cell and developmental biology · 2023
    Review
  5. Article
  6. NRG4-ErbB4 signaling represses proinflammatory macrophage activity.American journal of physiology. Gastrointestinal and liver physiology · 2021
    Article
  7. Review
  8. Article
  9. Article
  10. Role of ADAM10 in intestinal crypt homeostasis and tumorigenesis.Biochimica et biophysica acta. Molecular cell research · 2017
    Review
  11. Article
  12. Article
  13. ADAM17 is a Tumor Promoter and Therapeutic Target in Western Diet-associated Colon Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  14. Article
  15. Article
  16. ADAM Proteases and Gastrointestinal Function.Annual review of physiology · 2016
    Review
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

9 authors at 2 institutions in 1 country.

Yongjia FengSection of Pediatric Surgery, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Yu-Hwai TsaiDivision of Gastroenterology, Department of Pediatrics, University of Michigan Medical School, Ann Arbor, Michigan, USA Department of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Weidong XiaoSection of Pediatric Surgery, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Matthew W RallsSection of Pediatric Surgery, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Alex StoeckDivision of Gastroenterology, Department of Pediatrics, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Carole L WilsonDepartment of Pathology, University of Washington, Seattle, Washington, USA.
Elaine W RainesDepartment of Pathology, University of Washington, Seattle, Washington, USA.
Daniel H TeitelbaumSection of Pediatric Surgery, Department of Surgery, University of Michigan Medical School, Ann Arbor, Michigan, USA dttlbm@med.umich.edu peter.dempsey@ucdenver.edu.
Peter J DempseyDivision of Gastroenterology, Department of Pediatrics, University of Michigan Medical School, Ann Arbor, Michigan, USA Department of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, USA Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, University of Colorado Medical School, Aurora, Colorado, USA dttlbm@med.umich.edu peter.dempsey@ucdenver.edu.
University of Michigan–Ann Arbor · USUniversity of Washington · US

Funding

PUBLIC HEALTH DEMONSTRATIONP60DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MYERS, MARTIN G · 1985 to 2012
$26.5M
Role of ADAMs in Endothelial Inflammatory ResponseR01HL067267 · NHLBI · UNIVERSITY OF WASHINGTON · PI BORNFELDT, KARIN E. · 2002 to 2015
$3.9M
TPN INDUCED CHANGES IN INTRAEPITHELIAL LYMPHOCYTESR01AI044076 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TEITELBAUM, DANIEL H · 2004 to 2014
$3.2M
ADAM10 in Intestinal Homeostasis and RegenerationR01DK093697 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DEMPSEY, PETER J · 2012 to 2016
$1.5M
NHLBI NIH HHS R01 HL067267NHLBI NIH HHS R01-HL067267NIAID NIH HHS R01 AI044076NIAID NIH HHS R01-AI044076NIDDK NIH HHS P60 DK020572NIDDK NIH HHS P60DK020572NIDDK NIH HHS R01 DK093697NIDDK NIH HHS R01-DK093697
6 · The paper itself

Abstract

Total parenteral nutrition (TPN) is commonly used clinically to sustain patients; however, TPN is associated with profound mucosal atrophy, which may adversely affect clinical outcomes. Using a mouse TPN model, removing enteral nutrition leads to decreased crypt proliferation, increased intestinal epithelial cell (IEC) apoptosis and increased mucosal tumor necrosis factor alpha (TNF-α) expression that ultimately produces mucosal atrophy. Upregulation of TNF-α signaling plays a central role in mediating TPN-induced mucosal atrophy without intact epidermal growth factor receptor (EGFR) signaling. Currently, the mechanism and the tissue-specific contributions of TNF-α signaling to TPN-induced mucosal atrophy remain unclear. ADAM17 is an ectodomain sheddase that can modulate the signaling activity of several cytokine/growth factor receptor families, including the TNF-α/TNF receptor and ErbB ligand/EGFR pathways. Using TPN-treated IEC-specific ADAM17-deficient mice, the present study demonstrates that a loss of soluble TNF-α signaling from IECs attenuates TPN-induced mucosal atrophy. Importantly, this response remains dependent on the maintenance of functional EGFR signaling in IECs. TNF-α blockade in wild-type mice receiving TPN confirmed that soluble TNF-α signaling is responsible for downregulation of EGFR signaling in IECs. These results demonstrate that ADAM17-mediated TNF-α signaling from IECs has a significant role in the development of the proinflammatory state and mucosal atrophy observed in TPN-treated mice.

Indexed as

Signal TransductionADAM17 ProteinADAM ProteinsAnimalsApoptosisAtrophyCell ProliferationCytokinesErbB ReceptorsFemaleGene Knockout TechniquesHumansIntestinal MucosaMaleMiceMice, Inbred C57BLADAM17 ProteinADAM17 protein, humanAdam17 protein, mouseADAM ProteinsCytokinesErbB ReceptorsSTAT3 Transcription FactorTumor Necrosis Factor-alpha

Identifiers

PMID26283731
PMCPMC4589604
OpenAlexW2222692732

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.