Evidence map›Paper›PMID 32245801›Full record

ArticleDiabetes2020

Secretory Functions of Macrophages in the Human Pancreatic Islet Are Regulated by Endogenous Purinergic Signaling.

Jonathan R Weitz, Carol Jacques-Silva, Mirza Muhammed Fahd Qadir, Oliver Umland, Elizabeth Pereira, Farhan Qureshi, Alejandro Tamayo, Juan Dominguez-Bendala, Rayner Rodriguez-Diaz, Joana Almaça and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

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  19. Islet Inflammation and β Cell Dysfunction in Type 2 Diabetes.Handbook of experimental pharmacology · 2022
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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

11 authors at 1 institution in 1 country.

Jonathan R WeitzDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Miami Miller School of Medicine, Miami, FL jrw64@med.miami.edu jalmaca@med.miami.edu acaicedo@med.miami.edu.ORCID 0000-0003-0216-7990
Carol Jacques-SilvaDiabetes Research Institute, University of Miami Miller School of Medicine, Miami, FL.
Mirza Muhammed Fahd QadirDiabetes Research Institute, University of Miami Miller School of Medicine, Miami, FL.
Oliver UmlandDiabetes Research Institute, University of Miami Miller School of Medicine, Miami, FL.
Elizabeth PereiraDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Miami Miller School of Medicine, Miami, FL.
Farhan QureshiDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Miami Miller School of Medicine, Miami, FL.
Alejandro TamayoDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Miami Miller School of Medicine, Miami, FL.
Juan Dominguez-BendalaDiabetes Research Institute, University of Miami Miller School of Medicine, Miami, FL.ORCID 0000-0001-9410-9143
Rayner Rodriguez-DiazDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Miami Miller School of Medicine, Miami, FL.
Joana AlmaçaDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Miami Miller School of Medicine, Miami, FL jrw64@med.miami.edu jalmaca@med.miami.edu acaicedo@med.miami.edu.ORCID 0000-0002-9316-712X
Alejandro CaicedoDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Miami Miller School of Medicine, Miami, FL jrw64@med.miami.edu jalmaca@med.miami.edu acaicedo@med.miami.edu.ORCID 0000-0002-3765-3529
University of Miami · US

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
The delta cell as a key regulator of pancreatic islet biologyR01DK124527 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI RODRIGUEZ-DIAZ, RAYNER · 2020 to 2024
$1.9M
The Role of Innervation for Hormone Secretion in Human IsletsR01DK084321 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI CAICEDO, ALEJANDRO · 2011 to 2015
$1.8M
Harnessing Innervation to Promote Pancreatic Islet FunctionR01DK113093 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI CAICEDO, ALEJANDRO · 2017 to 2020
$1.5M
Cholinergic signaling in the human pancreatic isletR01DK111538 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI CAICEDO, ALEJANDRO · 2016 to 2018
$1.2M
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
The role of the delta cell in islet homeostasisR21DK114418 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI RODRIGUEZ-DIAZ, RAYNER · 2017 to 2019
$576k
Imaging mitochondrial signaling in B-cells ectopically implanted in the eyeR21ES025673 · NIEHS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI CAICEDO, ALEJANDRO, MORAES, CARLOS TORRES · 2015 to 2017
$569k
The Role of Innervation for Hormone Secretion in Human IsletsR56DK084321 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI CAICEDO, ALEJANDRO · 2009 to 2016
$306k
NIDDK NIH HHS K01 DK111757NIDDK NIH HHS R01 DK084321NIDDK NIH HHS R01 DK111538NIDDK NIH HHS R01 DK113093NIDDK NIH HHS R01 DK124527NIDDK NIH HHS R21 DK114418NIDDK NIH HHS R56 DK084321NIDDK NIH HHS U01 DK120456NIEHS NIH HHS R21 ES025673NIEHS NIH HHS R33 ES025673
6 · The paper itself

Abstract

Endocrine cells of the pancreatic islet interact with their microenvironment to maintain tissue homeostasis. Communication with local macrophages is particularly important in this context, but the homeostatic functions of human islet macrophages are not known. In this study, we show that the human islet contains macrophages in perivascular regions that are the main local source of the anti-inflammatory cytokine interleukin-10 (IL-10) and the metalloproteinase MMP9. Macrophage production and secretion of these homeostatic factors are controlled by endogenous purinergic signals. In obese and diabetic states, macrophage expression of purinergic receptors MMP9 and IL-10 is reduced. We propose that in those states, exacerbated β-cell activity due to increased insulin demand and increased cell death produce high levels of ATP that downregulate purinergic receptor expression. Loss of ATP sensing in macrophages may reduce their secretory capacity.

Indexed as

AnimalsAntigens, CDCalciumCytokinesCytosolDiabetes MellitusDown-RegulationGene Expression RegulationHumansIslets of LangerhansMacrophagesMicePurinesReceptors, PurinergicSignal TransductionTranscriptomeAntigens, CDCalciumCytokinesPurinesReceptors, Purinergic

Identifiers

PMID32245801
PMCPMC7243286
OpenAlexW3015074703

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.