Evidence map›Paper›PMID 40395933›Full record

ArticleFrontiers in cell and developmental biology2025

Generation and functional characterization of tuft cells in non-human primate pancreatic ducts through organoid culture systems.

Kosuke Sakaguchi, Chiemi Kimura-Nakajima, Akihiko Inaba, Yoshiko Hatano, Hanako Ogawa, Yuichi Koshiishi, Keisuke Tanaka, Tatsuya Kometani, Makoto Ohmoto, Koji Sato and 2 more

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Animal organoids as models for integrated One Health research.One health (Amsterdam, Netherlands) · 2026
    Review
  2. 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

12 authors.

Kosuke SakaguchiFaculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Chiemi Kimura-NakajimaFaculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Akihiko InabaGraduate School of Science, Osaka University, Suita, Ōsaka, Japan.
Yoshiko HatanoFaculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Hanako OgawaFaculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Yuichi KoshiishiFaculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Keisuke TanakaFaculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Tatsuya KometaniFaculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Makoto OhmotoFaculty of Health and Welfare, Takasaki University of Health and Welfare, Takasaki, Gunma, Japan.
Koji SatoDepartment of Applied Biological Chemistry, The University of Tokyo, Tokyo, Japan.
Hiroo ImaiCenter for the Evolutionary Origins of Human Behavior, Kyoto University, Kyoto, Japan.
Ken IwatsukiFaculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pancreatic duct plays a key role in collecting pancreatic juice, which is rich in digestive enzymes. The fluid flows unidirectionally into the duodenum, where it mixes with partially digested food to further facilitate digestion. In this study, we report the generation of pancreatic ductal organoids from non-human primates for the first time, aimed at investigating the role of tuft cells that reside in the pancreatic duct since no studies have addressed the role of tuft cells in the pancreas. The organoids were maintained in a medium supplemented with Wnt3a, Noggin, R-spondin, and other factors that support pancreatic duct proliferation. These pancreatic organoids expressed the stem cell marker LGR5 mRNA and the ductal marker protein CK19, although tuft cell markers were not detectable at this stage. Upon stimulation with IL-4/13, tuft cell differentiation was confirmed by immunohistochemistry and transcriptomic analysis. We observed induction of DCLK1, as well as taste signaling molecules such as TRPM5 and PLCβ2, which are markers of type II taste cells. Additionally, upregulation of LYZ and DEFB1 mRNA indicated the expression of antimicrobial peptide markers, alongside molecules associated with inflammation. Furthermore, the differentiated organoids specifically responded to a bitter compound, suggesting that pancreatic tuft cells may play a role in detecting potentially harmful chemicals. Finally, immunohistochemical analysis identified tuft cells in the non-human primate pancreas, supporting their involvement in sensing harmful compounds and regulating protective responses within the pancreas.

Indexed as

organoidpancreasprimatetuft cellstype 2 immunity

Identifiers

PMID40395933
PMCPMC12089129

What Socratic holds

Textmetadata
LicenceCC BY
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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.