Evidence map›Paper›PMID 39885637›Full record

ArticleThe International journal of artificial organs2025

Hepatic conditioning results in better lung endothelial cell preservation under hypoxic environment in vitro.

Kentaro Noda, Neha Atale, Taylor Austin, David A Geller, Jorg Gerlach, Pablo G Sanchez

Abstract read
In one paragraph

Article in The International journal of artificial organs, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

6 authors.

Kentaro NodaDepartment of Cardiothoracic Surgery, University of Pittsburgh Medical Center Health System, Pittsburgh, PA, USA.ORCID 0000-0001-8921-1944
Neha AtaleDepartment of Cardiothoracic Surgery, University of Pittsburgh Medical Center Health System, Pittsburgh, PA, USA.
Taylor AustinDepartment of Surgery, University of Pittsburgh Medical Center Health System, Pittsburgh, PA, USA.
David A GellerDepartment of Surgery, University of Pittsburgh Medical Center Health System, Pittsburgh, PA, USA.
Jorg GerlachDepartment of Surgery, University of Pittsburgh Medical Center Health System, Pittsburgh, PA, USA.
Pablo G SanchezDepartments of Surgery and Bioengineering, McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0003-3607-0345

Funding

Incorporating hepatic cell function into lung ex vivo lung perfusion for transplant preservationR21HL164436 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GERLACH, JOERG C., SANCHEZ, PABLO G · 2023 to 2024
$437k
NHLBI NIH HHS R21 HL164436
6 · The paper itself

Abstract

backgroundas we look to extend

methodswe performed in vitro experiments using human lung microvascular endothelial cells (HLMVECs), human hepatocytes, and perfusate (Steen solution). Four experimental groups: 1) fresh Steen (negative controls, NC), 2) EVLP'ed Steen control, this solution collected after 12 h of EVLP of human lungs, 3) hepatocyte conditioned EVLP'ed Steen (Hep-cond.), and 4) a RAGE inhibitor added in EVLP'ed Steen (RAGE inhibitor). HLMVECs were incubated in each testing condition and exposed to hypoxia (1% O

resultsHLMVECs incubated under hypoxia in EVLP'ed Steen showed significantly upregulated NF-κB signal and endothelial damage denoted by increased glycosaminoglycans and matrix metalloproteinase-2 activity among the groups. The Hep-cond. solution significantly attenuated those findings, while the RAGE inhibitor attenuated the NF-κB signal but not endothelial glycocalyx damage.

conclusionOur study demonstrates that hepatic function incorporated into EVLP can ameliorate pulmonary endothelial cells injury under hypoxic normothermic perfusion exposure. Our data supports the concept of incorporating other organ functions into an organ perfusion platform, to enhance lung graft preservation.

Indexed as

Endothelial CellsHepatocytesLungOrgan PreservationCell HypoxiaCells, CulturedHumansNF-kappa BOrgan Preservation SolutionsPerfusionReceptor for Advanced Glycation End ProductsSignal TransductionNF-kappa BOrgan Preservation SolutionsReceptor for Advanced Glycation End Productsendothelial dysfunctionex vivo lung perfusionhepatic supportlung preservationLung transplantation

Identifiers

PMID39885637
PMCPMC12355480

What OpenQuestion holds

Textmetadata
LicenceTDM
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.