Evidence map›Paper›PMID 39298538›Full record

ArticleIslets2024

EndoC-βH3 pseudoislets are suitable for intraportal transplantation in diabetic mice.

Mengmeng Zhou, Thomas Linn, Sebastian Friedrich Petry

Abstract read
In one paragraph

Article in Islets, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Mengmeng ZhouClinical Research Unit and Working Group Experimental Diabetology and Islet Cell Biology, Medical Clinic and Polyclinic III, Center of Internal Medicine, Justus Liebig University, Gießen, Germany.ORCID 0009-0007-6546-6548
Thomas LinnClinical Research Unit and Working Group Experimental Diabetology and Islet Cell Biology, Medical Clinic and Polyclinic III, Center of Internal Medicine, Justus Liebig University, Gießen, Germany.ORCID 0000-0002-0870-8164
Sebastian Friedrich PetryClinical Research Unit and Working Group Experimental Diabetology and Islet Cell Biology, Medical Clinic and Polyclinic III, Center of Internal Medicine, Justus Liebig University, Gießen, Germany.ORCID 0000-0002-3496-9894

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIslet or β-cell transplantation is a therapeutical approach to substitute the insulin-producing cells which are abolished in type 1 diabetes mellitus. The shortage of human islets as well as the complicated and costly isolation process limit the application of these techniques in daily clinical practice. EndoC-βH is a human β-cell line that readily forms aggregates termed pseudoislets, providing an alternative to primary human islets or β-cells.

methodsEndoC-βH3 cells were seeded and incubated to form pseudoislets. Their insulin secretion was analyzed by ELISA and compared with cell monolayers. Pseudoislets were transplanted into streptozotocin-treated NMRi nu/nu mice. Blood glucose was monitored before and after transplantation and compared with wild types. Grafts were analyzed by immunohistology.

resultsThis study shows that EndoC-βH cells are able to form pseudoislets by aggregation, leading to an enhanced glucose stimulated insulin secretion in vitro. These pseudoislets were then successfully transplanted into the livers of diabetic mice and produced insulin in vitro. Blood glucose levels of the streptozocin-treated recipient mice were significantly decreased when compared to pre-transplantation and matched the levels found in control mice.

conclusionWe suggest pseudoislets aggregated from EndoC-βH cells as a valuable and promising model for islet transplantation research.

Indexed as

Blood GlucoseDiabetes Mellitus, ExperimentalInsulinInsulin-Secreting CellsIslets of Langerhans TransplantationAnimalsCell AggregationCell LineDiabetes Mellitus, Type 1HumansInsulin SecretionMaleMiceMice, NudeBlood GlucoseInsulinEndoChumanhuman-to-mouseislet transplantationpseudoisletsstreptozotocintype 1 diabetes mellitus

Identifiers

PMID39298538
PMCPMC12135693

What Socratic holds

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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.