Evidence map›Paper›PMID 39779976›Full record

ArticleExperimental & molecular medicine2025

Pancreatic organogenesis mapped through space and time.

Marissa A Scavuzzo, Wojciech J Szlachcic, Matthew C Hill, Natalia M Ziojla, Jessica Teaw, Jeffrey C Carlson, Jonathan Tiessen, Jolanta Chmielowiec, James F Martin, Malgorzata Borowiak

Abstract read
In one paragraph

Article in Experimental & molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. 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

10 authors.

Marissa A Scavuzzo *Program in Developmental Biology, Baylor College of Medicine, Houston, TX, USA.
Wojciech J Szlachcic *Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.
Matthew C HillProgram in Developmental Biology, Baylor College of Medicine, Houston, TX, USA.
Natalia M ZiojlaInstitute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.
Jessica TeawCenter for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, and Houston Methodist Hospital, Houston, TX, USA.
Jeffrey C CarlsonProgram in Developmental Biology, Baylor College of Medicine, Houston, TX, USA.
Jonathan TiessenProgram in Developmental Biology, Baylor College of Medicine, Houston, TX, USA.
Jolanta ChmielowiecCenter for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, and Houston Methodist Hospital, Houston, TX, USA.
James F MartinProgram in Developmental Biology, Baylor College of Medicine, Houston, TX, USA.
Malgorzata BorowiakProgram in Developmental Biology, Baylor College of Medicine, Houston, TX, USA. malgorzata.borowiak@amu.edu.pl.

Funding

Fondation Leducq 14CVD01Fundacja na rzecz Nauki Polskiej (Foundation for Polish Science) POIR.04.04.00-00-20C5/16-00Howard Hughes Medical Institute (HHMI) Hanna H. Gray FellowshipNarodowe Centrum Nauki (National Science Centre) UMO-2020/37/B/NZ3/01917Narodowe Centrum Nauki (National Science Centre) UMO-2021/43/D/NZ3/02294New York Stem Cell Foundation (NYSCF) Druckenmiller Fellowship
6 · The paper itself

Abstract

The spatial organization of cells within a tissue is dictated throughout dynamic developmental processes. We sought to understand whether cells geometrically coordinate with one another throughout development to achieve their organization. The pancreas is a complex cellular organ with a particular spatial organization. Signals from the mesenchyme, neurons, and endothelial cells instruct epithelial cell differentiation during pancreatic development. To understand the cellular diversity and spatial organization of the developing pancreatic niche, we mapped the spatial relationships between single cells over time. We found that four transcriptionally unique subtypes of mesenchyme in the developing pancreas spatially coordinate throughout development, with each subtype at fixed locations in space and time in relation to other cells, including beta cells, vasculature, and epithelial cells. Our work provides insight into the mechanisms of pancreatic development by showing that cells are organized in a space and time manner.

Indexed as

OrganogenesisPancreasAnimalsCell DifferentiationGene Expression Regulation, DevelopmentalInsulin-Secreting CellsMesodermMice

Identifiers

PMID39779976
PMCPMC11799519

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.