Evidence map›Paper›PMID 28407355›Full record

ArticleLiver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society2017

Extracellular vesicles from bone marrow-derived mesenchymal stem cells protect against murine hepatic ischemia/reperfusion injury.

Hiroaki Haga, Irene K Yan, David A Borrelli, Akiko Matsuda, Mansi Parasramka, Neha Shukla, David D Lee, Tushar Patel

Open access · bronzeAbstract read
In one paragraph

Article in Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 3 pooled it
5.7field-weighted citation impact, top 3% 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

69 citing papers in PubMed, 3 syntheses or guidelines pooled it, 121 citations in OpenAlex.

  1. Pooled it
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  4. Endogenous Engineering Reprograms Extracellular Vesicles for Enhanced Therapeutic Function.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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9 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Hiroaki HagaDepartments of Transplantation and Cancer Biology, Mayo Clinic, Jacksonville, Florida.
Irene K YanDepartments of Transplantation and Cancer Biology, Mayo Clinic, Jacksonville, Florida.
David A BorrelliDepartments of Transplantation and Cancer Biology, Mayo Clinic, Jacksonville, Florida.
Akiko MatsudaDepartments of Transplantation and Cancer Biology, Mayo Clinic, Jacksonville, Florida.
Mansi ParasramkaDepartments of Transplantation and Cancer Biology, Mayo Clinic, Jacksonville, Florida.
Neha ShuklaDepartments of Transplantation and Cancer Biology, Mayo Clinic, Jacksonville, Florida.
David D LeeDepartments of Transplantation and Cancer Biology, Mayo Clinic, Jacksonville, Florida.
Tushar PatelDepartments of Transplantation and Cancer Biology, Mayo Clinic, Jacksonville, Florida.
Mayo Clinic in Florida · US

Funding

Extracellular non-coding RNA biomarkers of hepatocellular cancerUH3TR000884 · NCATS · MAYO CLINIC JACKSONVILLE · PI PATEL, TUSHAR · 2015 to 2017
$3.0M
NCATS NIH HHS UH3 TR000884
6 · The paper itself

Abstract

Hepatic ischemia/reperfusion injury (IRI) and associated inflammation contributes to liver dysfunction and complications after liver surgery and transplantation. Mesenchymal stem cells (MSCs) have been reported to reduce hepatic IRI because of their reparative immunomodulatory effects in injured tissues. Recent studies have highlighted beneficial effects of extracellular vesicles from mesenchymal stem cells (MSC-EV) on tissue injury. The effects of systemically administered mouse bone marrow-derived MSC-EV were evaluated in an experimental murine model of hepatic IRI induced by cross-clamping the hepatic artery and portal vein for 90 minutes followed by reperfusion for periods of up to 6 hours. Compared with controls, intravenous administration of MSC-EV 30 minutes prior to IRI dramatically reduced the extent of tissue necrosis, decreased caspase 3-positive and apoptotic cells, and reduced serum aminotransferase levels. MSC-EV increased hepatic messenger RNA (mRNA) expression of NACHT, LRR, and PYD domains-containing protein 12, and the chemokine (C-X-C motif) ligand 1, and reduced mRNA expression of several inflammatory cytokines such as interleukin 6 during IRI. MSC-EV increased cell viability and suppressed both oxidative injury and nuclear factor kappa B activity in murine hepatocytes in vitro. In conclusion, the administration of extracellular vesicles derived from bone marrow-derived MSCs may ameliorate hepatic IRI by reducing hepatic injury through modulation of the inflammatory response.Liver Transplantation 23 791-803 2017 AASLD.

Indexed as

Extracellular VesiclesAnimalsApoptosisBone Marrow CellsCaspase 3Cell SurvivalChemokine CXCL1Hepatic ArteryHepatocytesHypoxiaInflammationInterleukin-6Intracellular Signaling Peptides and ProteinsLiverMesenchymal Stem CellsMesenchymal Stem Cell TransplantationCasp3 protein, mouseCaspase 3Chemokine CXCL1Cxcl1 protein, mouseInterleukin-6interleukin-6, mouseIntracellular Signaling Peptides and ProteinsNF-kappa B p50 SubunitNfkb1 protein, mouseNLRP12 protein, mouseOxygenReactive Oxygen SpeciesTransaminases

Identifiers

PMID28407355
PMCPMC5495137
OpenAlexW2606388654

What OpenQuestion holds

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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.