Evidence map›Paper›PMID 37829188›Full record

ArticleGastro hep advances2022

Specific Temporal Requirement of Prox1 Activity During Pancreatic Acinar Cell Development.

Angelica S Martinez-Ramirez, Thomas L Borders, Leena Paul, Matthew Schipma, Xinkun Wang, Farida Korobova, Christopher V Wright, Beatriz Sosa-Pineda

Open access · goldAbstract read
In one paragraph

Article in Gastro hep advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 89% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 3 institutions in 1 country.

Angelica S Martinez-RamirezDepartment of Medicine, Feinberg Cardiovascular and Renal Research Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Thomas L BordersDepartment of Medicine, Feinberg Cardiovascular and Renal Research Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Leena PaulDepartment of Genetics, St. Jude Children's Research Hospital, Memphis, Tennessee.
Matthew SchipmaCenter for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Xinkun WangCenter for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Farida KorobovaCenter for Advanced Microscopy, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Christopher V WrightDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee.
Beatriz Sosa-PinedaDepartment of Medicine, Feinberg Cardiovascular and Renal Research Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Northwestern University · USSt. Jude Children's Research Hospital · USVanderbilt University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LEONIDAS C. PLATANIAS · 1993 to 2026
$153.9M
Development, cellular plasticity and homeostasis of the exocrine pancreasR01DK106266 · NIDDK · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SOSA-PINEDA, BEATRIZ · 2015 to 2018
$1.3M
NCI NIH HHS P30 CA060553NIDDK NIH HHS R01 DK106266
6 · The paper itself

Abstract

BACKGROUND AND

aimsAn interactive regulatory network assembled through the induction and downregulation of distinct transcription factors governs acinar cell maturation. Understanding how this network is built is relevant for protocols of directed pancreatic acinar differentiation. The murine transcription factor Prox1 is highly expressed in multipotent pancreatic progenitors and in various mature pancreatic cell types except for acinar cells. In this study, we investigated when is Prox1 expression terminated in developing acinar cells and the potential involvement of its activity in acinar cell specification/differentiation. We also investigated the effects of sustained Prox1 expression in acinar maturation and maintenance.

methodsProx1 acinar expression was analyzed by immunofluorescence and confocal microscopy.

resultsImmunostaining results reveal transient Prox1 expression in newly committed embryonic acinar cells. RNA-sequencing demonstrate precocious expression of multiple "late" acinar genes in the pancreas of

conclusionProx1 transient expression in early acinar cells is necessary for correct sequential gene expression. Prox1 expression is terminated in developing acinar cells to complete maturation and to preserve homeostasis.

Indexed as

Acinar CellMaturationProx1

Identifiers

PMID37829188
PMCPMC10569262
OpenAlexW4281551495

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.