Evidence map›Paper›PMID 25782016›Full record

ArticleJournal of cellular and molecular medicine2015

Controlled aggregation of primary human pancreatic islet cells leads to glucose-responsive pseudoislets comparable to native islets.

Janneke Hilderink, Siebe Spijker, Françoise Carlotti, Lydia Lange, Marten Engelse, Clemens van Blitterswijk, Eelco de Koning, Marcel Karperien, Aart van Apeldoorn

Open access · goldAbstract readComparative Study
In one paragraph

Article in Journal of cellular and molecular medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
6.2field-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

46 citing papers in PubMed, 77 citations in OpenAlex.

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  13. Formation of Re-Aggregated Neonatal Porcine Islet Clusters ImprovesTransplant international : official journal of the European Society for Organ Transplantation · 2022
    Article
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  16. Pancreatic Organoids for Regenerative Medicine and Cancer Research.Frontiers in cell and developmental biology · 2022
    Review
  17. Review
  18. Towards organoid culture without Matrigel.Communications biology · 2021
    Review
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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

9 authors at 2 institutions in 1 country.

Janneke HilderinkDepartment of Developmental Bioengineering, University of Twente, Enschede, The Netherlands.
Siebe SpijkerDepartment of Nephrology, Leiden University Medical Center, Leiden, The Netherlands.
Françoise CarlottiDepartment of Nephrology, Leiden University Medical Center, Leiden, The Netherlands.
Lydia LangeDepartment of Developmental Bioengineering, University of Twente, Enschede, The Netherlands.
Marten EngelseDepartment of Nephrology, Leiden University Medical Center, Leiden, The Netherlands.
Clemens van BlitterswijkDepartment of Tissue Regeneration, University of Twente, Enschede, The Netherlands.
Eelco de KoningDepartment of Nephrology, Leiden University Medical Center, Leiden, The Netherlands.
Marcel KarperienDepartment of Developmental Bioengineering, University of Twente, Enschede, The Netherlands.
Aart van ApeldoornDepartment of Developmental Bioengineering, University of Twente, Enschede, The Netherlands.ORCID http://orcid.org/0000-0002-2940-5699
University of Twente · NLLeiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinical islet transplantation is a promising treatment for patients with type 1 diabetes. However, pancreatic islets vary in size and shape affecting their survival and function after transplantation because of mass transport limitations. To reduce diffusion restrictions and improve islet cell survival, the generation of islets with optimal dimensions by dispersion followed by reassembly of islet cells, can help limit the length of diffusion pathways. This study describes a microwell platform that supports the controlled and reproducible production of three-dimensional pancreatic cell clusters of human donor islets. We observed that primary human islet cell aggregates with a diameter of 100-150 μm consisting of about 1000 cells best resembled intact pancreatic islets as they showed low apoptotic cell death (<2%), comparable glucose-responsiveness and increasing PDX1, MAFA and INSULIN gene expression with increasing aggregate size. The re-associated human islet cells showed an a-typical core shell configuration with beta cells predominantly on the outside unlike human islets, which became more randomized after implantation similar to native human islets. After transplantation of these islet cell aggregates under the kidney capsule of immunodeficient mice, human C-peptide was detected in the serum indicating that beta cells retained their endocrine function similar to human islets. The agarose microwell platform was shown to be an easy and very reproducible method to aggregate pancreatic islet cells with high accuracy providing a reliable tool to study cell-cell interactions between insuloma and/or primary islet cells.

Indexed as

AnimalsCell AggregationCell Line, TumorCells, CulturedCell SizeCell SurvivalFemaleGlucoseHumansInsulinomaIslets of LangerhansMaleMice, SCIDMiddle AgedReproducibility of ResultsGlucosebeta cellsisletspseudoislets bioengineeringtype 1 diabetes

Identifiers

PMID25782016
PMCPMC4549034
OpenAlexW2160639244

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.