Evidence map›Paper›PMID 31075154›Full record

ArticlePloS one2019

Distributions of endocrine cell clusters during porcine pancreatic development.

Masaki Nagaya, Asuka Hayashi, Kazuaki Nakano, Michiyo Honda, Koki Hasegawa, Kazutoshi Okamoto, Shiori Itazaki, Hitomi Matsunari, Masahito Watanabe, Kazuhiro Umeyama and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Masaki NagayaMeiji University International Institute for Bio-Resource Research, Kawasaki, Japan.ORCID 0000-0003-0784-5009
Asuka HayashiLaboratory of Developmental Engineering, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki, Japan.
Kazuaki NakanoMeiji University International Institute for Bio-Resource Research, Kawasaki, Japan.
Michiyo HondaMeiji University International Institute for Bio-Resource Research, Kawasaki, Japan.
Koki HasegawaLaboratory of Developmental Engineering, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki, Japan.
Kazutoshi OkamotoLaboratory of Developmental Engineering, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki, Japan.
Shiori ItazakiLaboratory of Developmental Engineering, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki, Japan.
Hitomi MatsunariMeiji University International Institute for Bio-Resource Research, Kawasaki, Japan.
Masahito WatanabeMeiji University International Institute for Bio-Resource Research, Kawasaki, Japan.
Kazuhiro UmeyamaMeiji University International Institute for Bio-Resource Research, Kawasaki, Japan.
Hiroshi NagashimaMeiji University International Institute for Bio-Resource Research, Kawasaki, Japan.
Meiji University · JPSt. Marianna University School of Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic islet xenotransplantation is a potential treatment for diabetes mellitus, and porcine pancreas may provide a readily available source of islets. Islets in juvenile pigs are smaller than those in young adult pigs, but the insulin content is very similar. In addition, as juvenile pigs are more easily reared in uncontaminated conditions, many researchers have conducted studies using pancreatic islets from juvenile pigs. We aimed to analyze the distributions of endocrine cell clusters by comprehensively evaluating juvenile porcine pancreatic development and to propose an appropriate age at which islets could be isolated from the juvenile porcine pancreas.

methodsSplenic (SL) and duodenal lobe (DL) samples were collected from the pancreases of pigs aged 0-180 days (n = 3/day after birth). The chronological changes in endocrine cell clustering were analyzed in relation to morphological changes, cell characterization, numbers, islet areas, and gene expression.

resultsIn juvenile pigs aged 0-21 days, the pancreas contained numerous endocrine cells, and compact islets appeared from 21 days of age. Well-defined small islets were seen at 28 days of age, and the clusters were denser in the SL than in the DL. At 35 days of age, the islets were morphologically similar to those observed at 180 days of age, and the greater number of islets was similar to that seen at 90 days of age. The differences in the islets' cytoarchitecture between the lobes were negligible. The expression of β-cell-related genes was higher in the juvenile pancreas than in the adult pancreas, and the expression of neurogenin-3 decreased dramatically over time.

conclusionsThese findings may have implications for attempts to refine the most appropriate age for islet isolation from porcine donors. Focusing on porcine pancreatic islets isolated at around 35 days after birth may offer benefits regarding their xenotransplantation potential.

Indexed as

Age FactorsAnimalsBasic Helix-Loop-Helix ProteinsCluster AnalysisDiabetes MellitusEndocrine CellsHumansIslets of LangerhansIslets of Langerhans TransplantationNerve Tissue ProteinsSwineTransplantation, HeterologousBasic Helix-Loop-Helix ProteinsNerve Tissue Proteins

Identifiers

PMID31075154
PMCPMC6510474
OpenAlexW2944288314

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Registered trials

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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.