Cytoprotective Effects of Mesenchymal Stem Cells During Liver Transplantation From Donors After Cardiac Death in Swine.


Journal

Transplantation proceedings
ISSN: 1873-2623
Titre abrégé: Transplant Proc
Pays: United States
ID NLM: 0243532

Informations de publication

Date de publication:
Historique:
received: 30 12 2019
accepted: 26 01 2020
pubmed: 12 5 2020
medline: 24 11 2020
entrez: 12 5 2020
Statut: ppublish

Résumé

Liver transplantation from donors after cardiac death (DCDs) can increase the pool of available organs. Recently, mesenchymal stem cells (MSCs) have been used to treat various diseases. Some studies have reported that MSCs improve the outcome of liver transplantation from DCDs in mice. The aim of this study was to evaluate the cytoprotective effects and safety of MSC transplantation on liver grafts from DCDs in swine. For the MSCs, we used swine adipose-derived stem cells (ADSCs). Landrace swine were divided into 3 groups (n = 5) as follows: 1. the heart-beating (HB) group, from which liver grafts were retrieved and transplanted; 2. the DCD group, from which liver grafts were retrieved 10 minutes after apnea-induced cardiac arrest and transplanted; and 3. the ADSC group, from which liver grafts were retrieved as with the DCD group, transplanted, and then infused with 1.0 × 10 In the HB group, all 5 recipients survived for >7 days, whereas all 5 recipients in the DCD group died within 24 hours after transplantation. In the ADSC group, 3 recipients survived for >7 days, whereas 2 recipients died within 4 days after transplantation. The survival rate was significantly higher in the ADSC group than in the DCD group. MSCs could protect the function of liver grafts from warm ischemia-reperfusion injury and improve the viability of DCD liver grafts.

Sections du résumé

BACKGROUND BACKGROUND
Liver transplantation from donors after cardiac death (DCDs) can increase the pool of available organs. Recently, mesenchymal stem cells (MSCs) have been used to treat various diseases. Some studies have reported that MSCs improve the outcome of liver transplantation from DCDs in mice. The aim of this study was to evaluate the cytoprotective effects and safety of MSC transplantation on liver grafts from DCDs in swine.
METHODS METHODS
For the MSCs, we used swine adipose-derived stem cells (ADSCs). Landrace swine were divided into 3 groups (n = 5) as follows: 1. the heart-beating (HB) group, from which liver grafts were retrieved and transplanted; 2. the DCD group, from which liver grafts were retrieved 10 minutes after apnea-induced cardiac arrest and transplanted; and 3. the ADSC group, from which liver grafts were retrieved as with the DCD group, transplanted, and then infused with 1.0 × 10
RESULTS RESULTS
In the HB group, all 5 recipients survived for >7 days, whereas all 5 recipients in the DCD group died within 24 hours after transplantation. In the ADSC group, 3 recipients survived for >7 days, whereas 2 recipients died within 4 days after transplantation. The survival rate was significantly higher in the ADSC group than in the DCD group.
CONCLUSIONS CONCLUSIONS
MSCs could protect the function of liver grafts from warm ischemia-reperfusion injury and improve the viability of DCD liver grafts.

Identifiants

pubmed: 32389486
pii: S0041-1345(19)31859-7
doi: 10.1016/j.transproceed.2020.01.165
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1891-1900

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Hideaki Sasajima (H)

Department of Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan. Electronic address: jimayei7720012000@yahoo.co.jp.

Shigehito Miyagi (S)

Department of Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.

Shuhei Yamada (S)

Department of Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.

Yuta Kakizaki (Y)

Department of Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.

Takashi Kamei (T)

Department of Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.

Michiaki Unno (M)

Department of Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.

Masafumi Goto (M)

Division of Transplantation and Regenerative Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.

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