Reduction of acute rejection by bone marrow mesenchymal stem cells during rat small bowel transplantation.

Bone marrow mesenchymal stem cells (BMMSCs) have shown immunosuppressive activity in transplantation. This study was designed to determine whether BMMSCs could improve outcomes of small bowel transplantation in rats.Heterotopic small bowel transplantation was performed from Brown Norway to Lewis rat...

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Main Authors: Yang Yang, Hong-Li Song, Wen Zhang, Ben-Juan Wu, Nan-Nan Fu, Wei-Ping Zheng, Chong Dong, Zhong-Yang Shen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4266507?pdf=render
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spelling doaj-c03376c0928b424283db0796a08ef1d22020-11-25T02:45:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01912e11452810.1371/journal.pone.0114528Reduction of acute rejection by bone marrow mesenchymal stem cells during rat small bowel transplantation.Yang YangHong-Li SongWen ZhangBen-Juan WuNan-Nan FuWei-Ping ZhengChong DongZhong-Yang ShenBone marrow mesenchymal stem cells (BMMSCs) have shown immunosuppressive activity in transplantation. This study was designed to determine whether BMMSCs could improve outcomes of small bowel transplantation in rats.Heterotopic small bowel transplantation was performed from Brown Norway to Lewis rats, followed by infusion of BMMSCs through the superficial dorsal veins of the penis. Controls included rats infused with normal saline (allogeneic control), isogeneically transplanted rats (BN-BN) and nontransplanted animals. The animals were sacrificed after 1, 5, 7 or 10 days. Small bowel histology and apoptosis, cytokine concentrations in serum and intestinal grafts, and numbers of T regulatory (Treg) cells were assessed at each time point.Acute cellular rejection occurred soon after transplantation and became aggravated over time in the allogeneic control rats, with increase in apoptosis, inflammatory response, and T helper (Th)1/Th2 and Th17/Treg-related cytokines. BMMSCs significantly attenuated acute cellular rejection, reduced apoptosis and suppressed the concentrations of interleukin (IL)-2, IL-6, IL-17, IL-23, tumor necrosis factor (TNF)-α, and interferon (IFN)-γ while upregulating IL-10 and transforming growth factor (TGF)-β expression and increasing Treg levels.BMMSCs improve the outcomes of allogeneic small bowel transplantation by attenuating the inflammatory response and acute cellular rejection. Treatment with BMMSCs may overcome acute cellular rejection in small bowel transplantation.http://europepmc.org/articles/PMC4266507?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yang Yang
Hong-Li Song
Wen Zhang
Ben-Juan Wu
Nan-Nan Fu
Wei-Ping Zheng
Chong Dong
Zhong-Yang Shen
spellingShingle Yang Yang
Hong-Li Song
Wen Zhang
Ben-Juan Wu
Nan-Nan Fu
Wei-Ping Zheng
Chong Dong
Zhong-Yang Shen
Reduction of acute rejection by bone marrow mesenchymal stem cells during rat small bowel transplantation.
PLoS ONE
author_facet Yang Yang
Hong-Li Song
Wen Zhang
Ben-Juan Wu
Nan-Nan Fu
Wei-Ping Zheng
Chong Dong
Zhong-Yang Shen
author_sort Yang Yang
title Reduction of acute rejection by bone marrow mesenchymal stem cells during rat small bowel transplantation.
title_short Reduction of acute rejection by bone marrow mesenchymal stem cells during rat small bowel transplantation.
title_full Reduction of acute rejection by bone marrow mesenchymal stem cells during rat small bowel transplantation.
title_fullStr Reduction of acute rejection by bone marrow mesenchymal stem cells during rat small bowel transplantation.
title_full_unstemmed Reduction of acute rejection by bone marrow mesenchymal stem cells during rat small bowel transplantation.
title_sort reduction of acute rejection by bone marrow mesenchymal stem cells during rat small bowel transplantation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Bone marrow mesenchymal stem cells (BMMSCs) have shown immunosuppressive activity in transplantation. This study was designed to determine whether BMMSCs could improve outcomes of small bowel transplantation in rats.Heterotopic small bowel transplantation was performed from Brown Norway to Lewis rats, followed by infusion of BMMSCs through the superficial dorsal veins of the penis. Controls included rats infused with normal saline (allogeneic control), isogeneically transplanted rats (BN-BN) and nontransplanted animals. The animals were sacrificed after 1, 5, 7 or 10 days. Small bowel histology and apoptosis, cytokine concentrations in serum and intestinal grafts, and numbers of T regulatory (Treg) cells were assessed at each time point.Acute cellular rejection occurred soon after transplantation and became aggravated over time in the allogeneic control rats, with increase in apoptosis, inflammatory response, and T helper (Th)1/Th2 and Th17/Treg-related cytokines. BMMSCs significantly attenuated acute cellular rejection, reduced apoptosis and suppressed the concentrations of interleukin (IL)-2, IL-6, IL-17, IL-23, tumor necrosis factor (TNF)-α, and interferon (IFN)-γ while upregulating IL-10 and transforming growth factor (TGF)-β expression and increasing Treg levels.BMMSCs improve the outcomes of allogeneic small bowel transplantation by attenuating the inflammatory response and acute cellular rejection. Treatment with BMMSCs may overcome acute cellular rejection in small bowel transplantation.
url http://europepmc.org/articles/PMC4266507?pdf=render
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