Evidence map›Paper›PMID 32324170›Full record

ArticleJCI insight2020

Pancreas tissue slices from organ donors enable in situ analysis of type 1 diabetes pathogenesis.

Julia K Panzer, Helmut Hiller, Christian M Cohrs, Joana Almaça, Stephen J Enos, Maria Beery, Sirlene Cechin, Denise M Drotar, John R Weitz, Jorge Santini and 10 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 85 citations in OpenAlex.

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  20. Paracrine Signaling by Pancreatic Islet Cilia.Current opinion in endocrine and metabolic research · 2024
    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

20 authors at 4 institutions in 3 countries.

Julia K PanzerPaul Langerhans Institute Dresden of the Helmholtz Zentrum München at the University Clinic Carl Gustav Carus of Technische Universität Dresden, Helmholtz Zentrum München, Neuherberg, Germany.
Helmut HillerDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Christian M CohrsPaul Langerhans Institute Dresden of the Helmholtz Zentrum München at the University Clinic Carl Gustav Carus of Technische Universität Dresden, Helmholtz Zentrum München, Neuherberg, Germany.
Joana AlmaçaDepartment of Medicine, Division of Metabolism, Endocrinology and Diabetes, and.
Stephen J EnosPaul Langerhans Institute Dresden of the Helmholtz Zentrum München at the University Clinic Carl Gustav Carus of Technische Universität Dresden, Helmholtz Zentrum München, Neuherberg, Germany.
Maria BeeryDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Sirlene CechinDiabetes Research Institute, University of Miami Miller School of Medicine, Miami, Florida, USA.
Denise M DrotarPaul Langerhans Institute Dresden of the Helmholtz Zentrum München at the University Clinic Carl Gustav Carus of Technische Universität Dresden, Helmholtz Zentrum München, Neuherberg, Germany.
John R WeitzDepartment of Medicine, Division of Metabolism, Endocrinology and Diabetes, and.
Jorge SantiniJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, Florida, USA.
Mollie K HuberDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Mirza Muhammad Fahd QadirDiabetes Research Institute, University of Miami Miller School of Medicine, Miami, Florida, USA.
Ricardo L PastoriDiabetes Research Institute, University of Miami Miller School of Medicine, Miami, Florida, USA.
Juan Domínguez-BendalaDiabetes Research Institute, University of Miami Miller School of Medicine, Miami, Florida, USA.
Edward A PhelpsJ. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, Florida, USA.
Mark A AtkinsonDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Alberto PuglieseDepartment of Medicine, Division of Metabolism, Endocrinology and Diabetes, and.
Alejandro CaicedoDepartment of Medicine, Division of Metabolism, Endocrinology and Diabetes, and.
Irina KusmartsevaDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Stephan SpeierPaul Langerhans Institute Dresden of the Helmholtz Zentrum München at the University Clinic Carl Gustav Carus of Technische Universität Dresden, Helmholtz Zentrum München, Neuherberg, Germany.
University of Florida · USHelmholtz Zentrum München · DEUniversity of Miami · USDiabetes Australia · AU

Funding

In situ analysis of functional endocrine, vascular, and immune cell interactions during early postnatal development of the human pancreasU01DK120456 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BRISSOVA, MARCELA, CAICEDO, ALEJANDRO · 2018 to 2021
$2.6M
Interdisciplinary Graduate Program in Type 1 Diabetes and Biomedical EngineeringT32DK108736 · NIDDK · UNIVERSITY OF FLORIDA · PI MARK A. ATKINSON, Benjamin George Keselowsky · 2017 to 2026
$1.9M
Harnessing Innervation to Promote Pancreatic Islet FunctionR01DK113093 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI CAICEDO, ALEJANDRO · 2017 to 2020
$1.5M
Imaging mitochondrial signaling in B-cells ectopically implanted in the eyeR33ES025673 · NIEHS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI CAICEDO, ALEJANDRO, MORAES, CARLOS TORRES · 2018 to 2019
$761k
Role of pericytes in pancreatic islet fibrosisK01DK111757 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ALMACA, JOANA · 2017 to 2021
$694k
NIDDK NIH HHS U01 DK120456
6 · The paper itself

Abstract

In type 1 diabetes (T1D), autoimmune destruction of pancreatic β cells leads to insulin deficiency and loss of glycemic control. However, knowledge about human pancreas pathophysiology in T1D remains incomplete. To address this limitation, we established a pancreas tissue slice platform of donor organs with and without diabetes, facilitating the first live cell studies of human pancreas in T1D pathogenesis to our knowledge. We show that pancreas tissue slices from organ donors allow thorough assessment of processes critical for disease development, including insulin secretion, β cell physiology, endocrine cell morphology, and immune infiltration within the same donor organ. Using this approach, we compared detailed pathophysiological profiles for 4 pancreata from donors with T1D with 19 nondiabetic control donors. We demonstrate that β cell loss, β cell dysfunction, alterations of β cell physiology, and islet infiltration contributed differently to individual cases of T1D, allowing insight into pathophysiology and heterogeneity of T1D pathogenesis. Thus, our study demonstrates that organ donor pancreas tissue slices represent a promising and potentially novel approach in the search for successful prevention and reversal strategies of T1D.

Indexed as

Tissue Culture TechniquesAdolescentAdultChildChild, PreschoolDiabetes Mellitus, Type 1FemaleHumansInsulin-Secreting CellsMalePancreasTissue DonorsYoung AdultAutoimmune diseasesAutoimmunityBeta cellsDiabetesEndocrinology

Identifiers

PMID32324170
PMCPMC7205437
OpenAlexW3018833713

What OpenQuestion holds

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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.