Evidence map›Paper›PMID 34638521›Full record

ArticleInternational journal of molecular sciences2021

Exploring Insulin Production Following Alveolar Islet Transplantation (AIT).

Hien Lau, Tanja Khosrawipour, Shiri Li, Michael Alexander, Piotr Frelkiewicz, Maya Karine Labbé, Sven Stieglitz, Jonathan Robert Todd Lakey, Wojciech Kielan, Veria Khosrawipour

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 6 institutions in 3 countries.

Hien LauDepartment of Surgery, University of California, Irvine (UCI), Orange, CA 92868, USA.
Tanja KhosrawipourDepartment of Surgery (A), University-Hospital Düsseldorf, Heinrich-Heine University, Moorenstrasse 5, D-40225 Duesseldorf, Germany.
Shiri LiDepartment of Surgery, Weill Medical College of Cornell University, New York, NY 10065, USA.
Michael AlexanderDepartment of Surgery, University of California, Irvine (UCI), Orange, CA 92868, USA.
Piotr FrelkiewiczCenter for Experimental Diagnostics and Biomedical Innovations, Wroclaw University of Environmental and Life Sciences, 50-375 Wroclaw, Poland.
Maya Karine LabbéSchool of Dentistry, Wroclaw Medical University, 50-367 Wroclaw, Poland.
Sven StieglitzDepartment Pulmonary Medicine, Petrus-Hospital Wuppertal, University of Witten-Herdecke, D-42283 Wuppertal, Germany.
Jonathan Robert Todd LakeyDepartment of Surgery, University of California, Irvine (UCI), Orange, CA 92868, USA.
Wojciech Kielan2nd Department of General Surgery and Surgical Oncology, Wroclaw Medical University, 50-556 Wroclaw, Poland.
Veria KhosrawipourDepartment of Surgery, University of California, Irvine (UCI), Orange, CA 92868, USA.
University of California, Irvine · USWroclaw Medical University · PLCornell University · USHeinrich Heine University Düsseldorf · DEHelios Universitätsklinikum Wuppertal · DEWrocław University of Environmental and Life Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have demonstrated the feasibility of islet implantation into the alveoli. However, until today, there are no data on islet behavior and morphology at their transplant site. This study is the first to investigate islet distribution as well insulin production at the implant site. Using an ex vivo postmortem swine model, porcine pancreatic islets were isolated and aerosolized into the lung using an endoscopic spray-catheter. Lung tissue was explanted and bronchial airways were surgically isolated and connected to a perfusor. Correct implantation was confirmed via histology. The purpose of using this new lung perfusion model was to measure static as well as dynamic insulin excretions following glucose stimulation. Alveolar islet implantation was confirmed after aerosolization. Over 82% of islets were correctly implanted into the intra-alveolar space. The medium contact area to the alveolar surface was estimated at 60 +/- 3% of the total islet surface. The new constructed lung perfusion model was technically feasible. Following static glucose stimulation, insulin secretion was detected, and dynamic glucose stimulation revealed a biphasic insulin secretion capacity during perfusion. Our data indicate that islets secrete insulin following implantation into the alveoli and display an adapted response to dynamic changes in glucose. These preliminary results are encouraging and mark a first step toward endoscopically assisted islet implantation in the lung.

Indexed as

Administration, InhalationAerosolsAnimalsBlood GlucoseDiabetes Mellitus, Type 1GlucoseInsulinInsulin SecretionIslets of LangerhansIslets of Langerhans TransplantationPulmonary AlveoliSwineAerosolsBlood GlucoseGlucoseInsulinaerosoldrug deliveryinsulinisletlungtransplantationxenograft

Identifiers

PMID34638521
PMCPMC8508311
OpenAlexW3199010673

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.