Evidence map›Paper›PMID 15024058›Full record

ArticleMolecular and cellular biology2004

Inhibition of Mist1 homodimer formation induces pancreatic acinar-to-ductal metaplasia.

Liqin Zhu, Thai Tran, J Michael Rukstalis, Peichuan Sun, Barbara Damsz, Stephen F Konieczny

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
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  3. Review
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  5. Be like water, my cells: cell plasticity and the art of transformation.Frontiers in cell and developmental biology · 2023
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Acinar cell plasticity and development of pancreatic ductal adenocarcinoma.Nature reviews. Gastroenterology & hepatology · 2017
    Review
  14. Article
  15. Review
  16. Article
  17. Article
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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

6 authors at 1 institution in 1 country.

Liqin ZhuDepartment of Biological Sciences, Purdue University, West Lafayette, Indiana 47907-1392, USA.
Thai Tran
J Michael Rukstalis
Peichuan Sun
Barbara Damsz
Stephen F Konieczny
Purdue University West Lafayette · US

Funding

Pancreas Transcription Factors and Disease Model SystemsR01DK055489 · NIDDK · PURDUE UNIVERSITY WEST LAFAYETTE · PI KONIECZNY, STEPHEN F · 2000 to 2017
$5.6M
NIDDK NIH HHS DK55489NIDDK NIH HHS R01 DK055489
6 · The paper itself

Abstract

The pancreas consists of three main cell lineages (endocrine, exocrine, and duct) that develop from common primitive foregut precursors. The transcriptional network responsible for endocrine cell development has been studied extensively, but much less is known about the transcription factors that maintain the exocrine and duct cell lineages. One transcription factor that may be important to exocrine cell function is Mist1, a basic helix-loop-helix (bHLH) factor that is expressed in acinar cells. In order to perform a molecular characterization of this protein, we employed coimmunoprecipitation and bimolecular fluorescence complementation assays, coupled with electrophoretic mobility shift assay studies, to show that Mist1 exists in vivo as a homodimer complex. Analysis of transgenic mice expressing a dominant-negative Mist1 transgene (Mist1(mutant basic) [Mist1(MB)]) revealed the cell autonomous effect of inhibiting endogenous Mist1. Mist1(MB) cells become disorganized, exhibit a severe depletion of intercellular gap junctions, and express high levels of the glycoprotein clusterin, which has been shown to demarcate immature acinar cells. Inhibition of Mist1 transcriptional activity also leads to activation of duct-specific genes, such as cytokeratin 19 and cytokeratin 20, suggesting that alterations in the bHLH network produce a direct acinar-to-ductal phenotypic switch in mature cells. We propose that Mist1 is a key transcriptional regulator of exocrine pancreatic cells and that in the absence of functional Mist1, acinar cells do not maintain their normal identity.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCell DifferentiationCell LineageClusterinConnexinsDimerizationGap Junction beta-1 ProteinGene Expression RegulationGenes, ReporterGlycoproteinsHelix-Loop-Helix MotifsMiceMice, TransgenicMolecular ChaperonesPancreasBasic Helix-Loop-Helix ProteinsBhlha15 protein, mouseClu protein, mouseClusterinConnexinsGap Junction beta-1 ProteinGlycoproteinsMolecular ChaperonesPancreatic ElastaseTranscription Factors

Identifiers

PMID15024058
PMCPMC371125
OpenAlexW2114278038

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.