Evidence map›Paper›PMID 31672937›Full record

ArticleJCI insight2019

iPreP is a three-dimensional nanofibrillar cellulose hydrogel platform for long-term ex vivo preservation of human islets.

Yi-Ju Chen, Taiji Yamazoe, Karla F Leavens, Fabian L Cardenas-Diaz, Andrei Georgescu, Dongeun Huh, Paul Gadue, Ben Z Stanger

Abstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

8 authors.

Yi-Ju ChenGastroenterology Division, Department of Medicine.
Taiji YamazoeGastroenterology Division, Department of Medicine.
Karla F LeavensCenter for Cellular and Molecular Therapeutics, Department of Pathology and Laboratory Medicine.
Fabian L Cardenas-DiazCenter for Cellular and Molecular Therapeutics, Department of Pathology and Laboratory Medicine.
Andrei GeorgescuDepartment of Bioengineering, School of Engineering and Applied Sciences, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Dongeun HuhDepartment of Bioengineering, School of Engineering and Applied Sciences, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Paul GadueCenter for Cellular and Molecular Therapeutics, Department of Pathology and Laboratory Medicine.
Ben Z StangerGastroenterology Division, Department of Medicine.

Funding

Integrated Islet Distribution Program (U24) - 2021U24DK098085 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI Carmella Evans-Molina, Joyce Carol Niland · 2021 to 2026
$17.8M
Translational Research Training in Pediatric Diabetes & EndocrinologyT32DK063688 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI LORRAINE E LEVITT KATZ, ANDREA Bridget KELLY · 2002 to 2026
$5.4M
A vascularized 3D biomimetic for islet function and physiologyUC4DK104196 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI CHEN, CHRISTOPHER S, GADUE, PAUL J · 2014 to 2016
$5.1M
Career Development Program in Pediatric Diabetes Research (K12) at CHOPK12DK094723 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI WILLI, STEVEN M · 2011 to 2020
$3.6M
Microphysiological systems for modeling autoimmunity in type 1 diabetesUG3DK122644 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI GADUE, PAUL J, HUH, DONGEUN · 2019 to 2020
$2.3M
NIDDK NIH HHS K12 DK094723NIDDK NIH HHS T32 DK063688NIDDK NIH HHS U24 DK098085NIDDK NIH HHS UC4 DK104196NIDDK NIH HHS UG3 DK122644
6 · The paper itself

Abstract

Islet transplantation is an effective therapy for achieving and maintaining normoglycemia in patients with type 1 diabetes mellitus. However, the supply of transplantable human islets is limited. Upon removal from the pancreas, islets rapidly disintegrate and lose function, resulting in a short interval for studies of islet biology and pretransplantation assessment. Here, we developed a biomimetic platform that can sustain human islet physiology for a prolonged period ex vivo. Our approach involved the creation of a multichannel perifusion system to monitor dynamic insulin secretion and intracellular calcium flux simultaneously, enabling the systematic evaluation of glucose-stimulated insulin secretion under multiple conditions. Using this tool, we developed a nanofibrillar cellulose hydrogel-based islet-preserving platform (iPreP) that can preserve islet viability, morphology, and function for nearly 12 weeks ex vivo, and with the ability to ameliorate glucose levels upon transplantation into diabetic hosts. Our platform has potential applications in the prolonged maintenance of human islets, providing an expanded time window for pretransplantation assessment and islet studies.

Indexed as

Islets of LangerhansAdolescentAdultCelluloseFemaleHumansHydrogelsIn Vitro TechniquesIslets of Langerhans TransplantationMaleMiddle AgedNanofibersPreservation, BiologicalCelluloseHydrogelsDiabetesEndocrinologyIslet cells

Identifiers

PMID31672937
PMCPMC6948755

What Socratic holds

Textmetadata
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.