Evidence map›Paper›PMID 30996131›Full record

ArticleJCI insight2019

Human duct cells contribute to β cell compensation in insulin resistance.

Ercument Dirice, Dario F De Jesus, Sevim Kahraman, Giorgio Basile, Raymond Ws Ng, Abdelfattah El Ouaamari, Adrian Kee Keong Teo, Shweta Bhatt, Jiang Hu, Rohit N Kulkarni

Open access · goldAbstract 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 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
11.3field-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

34 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
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  8. Beta-cell compensation and gestational diabetes.The Journal of biological chemistry · 2023
    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

10 authors at 1 institution in 2 countries.

Ercument DiriceSection of Islet Cell and Regenerative Biology, Joslin Diabetes Center, Boston, Massachusetts, USA.
Dario F De JesusSection of Islet Cell and Regenerative Biology, Joslin Diabetes Center, Boston, Massachusetts, USA.
Sevim KahramanSection of Islet Cell and Regenerative Biology, Joslin Diabetes Center, Boston, Massachusetts, USA.
Giorgio BasileSection of Islet Cell and Regenerative Biology, Joslin Diabetes Center, Boston, Massachusetts, USA.
Raymond Ws NgSection of Islet Cell and Regenerative Biology, Joslin Diabetes Center, Boston, Massachusetts, USA.
Abdelfattah El OuaamariSection of Islet Cell and Regenerative Biology, Joslin Diabetes Center, Boston, Massachusetts, USA.
Adrian Kee Keong TeoSection of Islet Cell and Regenerative Biology, Joslin Diabetes Center, Boston, Massachusetts, USA.
Shweta BhattSection of Islet Cell and Regenerative Biology, Joslin Diabetes Center, Boston, Massachusetts, USA.
Jiang HuSection of Islet Cell and Regenerative Biology, Joslin Diabetes Center, Boston, Massachusetts, USA.
Rohit N KulkarniSection of Islet Cell and Regenerative Biology, Joslin Diabetes Center, Boston, Massachusetts, USA.
Brigham and Women's Hospital · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI ROHIT N. KULKARNI · 1986 to 2026
$50.5M
Role of IGF-1 and Insulin Receptors Beta-Cell SurvivalR01DK067536 · NIDDK · JOSLIN DIABETES CENTER · PI ROHIT N. KULKARNI · 2004 to 2026
$8.0M
Role of SerpinB1 in beta cell growthR01DK103215 · NIDDK · JOSLIN DIABETES CENTER · PI KULKARNI, ROHIT N. · 2014 to 2018
$2.6M
Role of IGF-1 and insulin receptors beta-cell survivalR56DK067536 · NIDDK · JOSLIN DIABETES CENTER · PI KULKARNI, ROHIT N. · 2009 to 2010
$291k
NIDDK NIH HHS P30 DK036836NIDDK NIH HHS R01 DK067536NIDDK NIH HHS R01 DK103215NIDDK NIH HHS R56 DK067536
6 · The paper itself

Abstract

The identification of new sources of β cells is an important endeavor with therapeutic implications for diabetes. Insulin resistance, in physiological states such as pregnancy or in pathological states such as type 2 diabetes (T2D), is characterized by a compensatory increase in β cell mass. To explore the existence of a dynamic β cell reserve, we superimposed pregnancy on the liver-specific insulin receptor-KO (LIRKO) model of insulin resistance that already exhibits β cell hyperplasia and used lineage tracing to track the source of new β cells. Although both control and LIRKO mice displayed increased β cell mass in response to the relative insulin resistance of pregnancy, the further increase in mass in the latter supported a dynamic source that could be traced to pancreatic ducts. Two observations support the translational significance of these findings. First, NOD/SCID-γ LIRKO mice that became pregnant following cotransplantation of human islets and human ducts under the kidney capsule showed enhanced β cell proliferation and an increase in ductal cells positive for transcription factors expressed during β cell development. Second, we identified duct cells positive for immature β cell markers in pancreas sections from pregnant humans and in individuals with T2D. Taken together, during increased insulin demand, ductal cells contribute to the compensatory β cell pool by differentiation/neogenesis.

Indexed as

AdultAnimalsCell DifferentiationCell ProliferationDiabetes Mellitus, Type 2Disease Models, AnimalFemaleHumansInsulinInsulin ResistanceInsulin-Secreting CellsIslets of Langerhans TransplantationMiceMice, KnockoutMiddle AgedPancreatic DuctsInsulinReceptor, InsulinCell BiologyDiabetesEndocrinologyIslet cellsMouse models

Identifiers

PMID30996131
PMCPMC6538348
OpenAlexW2938533945

What OpenQuestion 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 OpenQuestion graph.