Cargando…

Induced Autologous Stem Cell Transplantation for Treatment of Rabbit Renal Interstitial Fibrosis

INTRODUCTION: Renal interstitial fibrosis (RIF) is a significant cause of end-stage renal failure. The goal of this study was to characterize the distribution of transplanted induced autologous stem cells in a rabbit model of renal interstitial fibrosis and evaluate its therapeutic efficacy for trea...

Descripción completa

Detalles Bibliográficos
Autores principales: Ruan, Guang-Ping, Xu, Fan, Li, Zi-An, Zhu, Guang-Xu, Pang, Rong-Qing, Wang, Jin-Xiang, Cai, Xue-Min, He, Jie, Yao, Xiang, Ruan, Guang-Hong, Xu, Xin-Ming, Pan, Xing-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867441/
https://www.ncbi.nlm.nih.gov/pubmed/24367598
http://dx.doi.org/10.1371/journal.pone.0083507
_version_ 1782296306994118656
author Ruan, Guang-Ping
Xu, Fan
Li, Zi-An
Zhu, Guang-Xu
Pang, Rong-Qing
Wang, Jin-Xiang
Cai, Xue-Min
He, Jie
Yao, Xiang
Ruan, Guang-Hong
Xu, Xin-Ming
Pan, Xing-Hua
author_facet Ruan, Guang-Ping
Xu, Fan
Li, Zi-An
Zhu, Guang-Xu
Pang, Rong-Qing
Wang, Jin-Xiang
Cai, Xue-Min
He, Jie
Yao, Xiang
Ruan, Guang-Hong
Xu, Xin-Ming
Pan, Xing-Hua
author_sort Ruan, Guang-Ping
collection PubMed
description INTRODUCTION: Renal interstitial fibrosis (RIF) is a significant cause of end-stage renal failure. The goal of this study was to characterize the distribution of transplanted induced autologous stem cells in a rabbit model of renal interstitial fibrosis and evaluate its therapeutic efficacy for treatment of renal interstitial fibrosis. METHODS: A rabbit model of renal interstitial fibrosis was established. Autologous fibroblasts were cultured, induced and labeled with green fluorescent protein (GFP). These labeled stem cells were transplanted into the renal artery of model animals at 8 weeks. RESULTS: Eight weeks following transplantation of induced autologous stem cells, significant reductions (P < 0.05) were observed in serum creatinine (SCr) (14.8 ± 1.9 mmol/L to 10.1 ± 2.1 mmol/L) and blood urea nitrogen (BUN) (119 ± 22 µmol/L to 97 ± 13 µmol/L), indicating improvement in renal function. CONCLUSIONS: We successfully established a rabbit model of renal interstitial fibrosis and demonstrated that transplantation of induced autologous stem cells can repair kidney damage within 8 weeks. The repair occurred by both inhibition of further development of renal interstitial fibrosis and partial reversal of pre-existing renal interstitial fibrosis. These beneficial effects lead to the development of normal tissue structure and improved renal function.
format Online
Article
Text
id pubmed-3867441
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-38674412013-12-23 Induced Autologous Stem Cell Transplantation for Treatment of Rabbit Renal Interstitial Fibrosis Ruan, Guang-Ping Xu, Fan Li, Zi-An Zhu, Guang-Xu Pang, Rong-Qing Wang, Jin-Xiang Cai, Xue-Min He, Jie Yao, Xiang Ruan, Guang-Hong Xu, Xin-Ming Pan, Xing-Hua PLoS One Research Article INTRODUCTION: Renal interstitial fibrosis (RIF) is a significant cause of end-stage renal failure. The goal of this study was to characterize the distribution of transplanted induced autologous stem cells in a rabbit model of renal interstitial fibrosis and evaluate its therapeutic efficacy for treatment of renal interstitial fibrosis. METHODS: A rabbit model of renal interstitial fibrosis was established. Autologous fibroblasts were cultured, induced and labeled with green fluorescent protein (GFP). These labeled stem cells were transplanted into the renal artery of model animals at 8 weeks. RESULTS: Eight weeks following transplantation of induced autologous stem cells, significant reductions (P < 0.05) were observed in serum creatinine (SCr) (14.8 ± 1.9 mmol/L to 10.1 ± 2.1 mmol/L) and blood urea nitrogen (BUN) (119 ± 22 µmol/L to 97 ± 13 µmol/L), indicating improvement in renal function. CONCLUSIONS: We successfully established a rabbit model of renal interstitial fibrosis and demonstrated that transplantation of induced autologous stem cells can repair kidney damage within 8 weeks. The repair occurred by both inhibition of further development of renal interstitial fibrosis and partial reversal of pre-existing renal interstitial fibrosis. These beneficial effects lead to the development of normal tissue structure and improved renal function. Public Library of Science 2013-12-18 /pmc/articles/PMC3867441/ /pubmed/24367598 http://dx.doi.org/10.1371/journal.pone.0083507 Text en © 2013 Ruan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ruan, Guang-Ping
Xu, Fan
Li, Zi-An
Zhu, Guang-Xu
Pang, Rong-Qing
Wang, Jin-Xiang
Cai, Xue-Min
He, Jie
Yao, Xiang
Ruan, Guang-Hong
Xu, Xin-Ming
Pan, Xing-Hua
Induced Autologous Stem Cell Transplantation for Treatment of Rabbit Renal Interstitial Fibrosis
title Induced Autologous Stem Cell Transplantation for Treatment of Rabbit Renal Interstitial Fibrosis
title_full Induced Autologous Stem Cell Transplantation for Treatment of Rabbit Renal Interstitial Fibrosis
title_fullStr Induced Autologous Stem Cell Transplantation for Treatment of Rabbit Renal Interstitial Fibrosis
title_full_unstemmed Induced Autologous Stem Cell Transplantation for Treatment of Rabbit Renal Interstitial Fibrosis
title_short Induced Autologous Stem Cell Transplantation for Treatment of Rabbit Renal Interstitial Fibrosis
title_sort induced autologous stem cell transplantation for treatment of rabbit renal interstitial fibrosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867441/
https://www.ncbi.nlm.nih.gov/pubmed/24367598
http://dx.doi.org/10.1371/journal.pone.0083507
work_keys_str_mv AT ruanguangping inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT xufan inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT lizian inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT zhuguangxu inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT pangrongqing inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT wangjinxiang inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT caixuemin inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT hejie inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT yaoxiang inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT ruanguanghong inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT xuxinming inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis
AT panxinghua inducedautologousstemcelltransplantationfortreatmentofrabbitrenalinterstitialfibrosis