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Establishing a tree shrew model of systemic lupus erythematosus and cell transplantation treatment

BACKGROUND: The establishment of a tree shrew model for systemic lupus erythematosus (SLE) provides a new method to evaluate the pathogenesis of autoimmune diseases. METHODS: Eighty tree shrews were randomly divided into four groups receiving either an intraperitoneal injection of pristane, lipopoly...

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Autores principales: Ruan, Guang-Ping, Yao, Xiang, Liu, Ju-Fen, He, Jie, Li, Zi-An, Yang, Jian-Yong, Pang, Rong-Qing, Pan, Xing-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995612/
https://www.ncbi.nlm.nih.gov/pubmed/27558022
http://dx.doi.org/10.1186/s13287-016-0385-1
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author Ruan, Guang-Ping
Yao, Xiang
Liu, Ju-Fen
He, Jie
Li, Zi-An
Yang, Jian-Yong
Pang, Rong-Qing
Pan, Xing-Hua
author_facet Ruan, Guang-Ping
Yao, Xiang
Liu, Ju-Fen
He, Jie
Li, Zi-An
Yang, Jian-Yong
Pang, Rong-Qing
Pan, Xing-Hua
author_sort Ruan, Guang-Ping
collection PubMed
description BACKGROUND: The establishment of a tree shrew model for systemic lupus erythematosus (SLE) provides a new method to evaluate the pathogenesis of autoimmune diseases. METHODS: Eighty tree shrews were randomly divided into four groups receiving either an intraperitoneal injection of pristane, lipopolysaccharide (LPS), or pristane and LPS, or no injection. Three weeks after injection, the SLE model tree shrews were divided into the model group and the treatment group. Tree shrews in the treatment group and the normal control group were infused with umbilical cord mesenchymal stem cells (UC-MSCs). The cells were labeled with DiR. Two weeks after transplantation, three groups of tree shrews were analyzed for urine protein, serum antinuclear antibodies and antiphospholipid, and inflammatory cytokine antibody microarray detection. The heart, liver, spleen, lung, and kidney were collected from the three groups and subjected to hematoxylin and eosin (HE) staining and detection of renal immune complex deposition. RESULTS: HE staining indicated pathology in the model group. Red fluorescence revealed immune complex deposition in the kidneys from the model group. CONCLUSIONS: The combined intraperitoneal injection of pristane and LPS is the best way to induce SLE pathological changes. The pathological changes improved after UC-MSC treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-016-0385-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-49956122016-08-25 Establishing a tree shrew model of systemic lupus erythematosus and cell transplantation treatment Ruan, Guang-Ping Yao, Xiang Liu, Ju-Fen He, Jie Li, Zi-An Yang, Jian-Yong Pang, Rong-Qing Pan, Xing-Hua Stem Cell Res Ther Research BACKGROUND: The establishment of a tree shrew model for systemic lupus erythematosus (SLE) provides a new method to evaluate the pathogenesis of autoimmune diseases. METHODS: Eighty tree shrews were randomly divided into four groups receiving either an intraperitoneal injection of pristane, lipopolysaccharide (LPS), or pristane and LPS, or no injection. Three weeks after injection, the SLE model tree shrews were divided into the model group and the treatment group. Tree shrews in the treatment group and the normal control group were infused with umbilical cord mesenchymal stem cells (UC-MSCs). The cells were labeled with DiR. Two weeks after transplantation, three groups of tree shrews were analyzed for urine protein, serum antinuclear antibodies and antiphospholipid, and inflammatory cytokine antibody microarray detection. The heart, liver, spleen, lung, and kidney were collected from the three groups and subjected to hematoxylin and eosin (HE) staining and detection of renal immune complex deposition. RESULTS: HE staining indicated pathology in the model group. Red fluorescence revealed immune complex deposition in the kidneys from the model group. CONCLUSIONS: The combined intraperitoneal injection of pristane and LPS is the best way to induce SLE pathological changes. The pathological changes improved after UC-MSC treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-016-0385-1) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-24 /pmc/articles/PMC4995612/ /pubmed/27558022 http://dx.doi.org/10.1186/s13287-016-0385-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ruan, Guang-Ping
Yao, Xiang
Liu, Ju-Fen
He, Jie
Li, Zi-An
Yang, Jian-Yong
Pang, Rong-Qing
Pan, Xing-Hua
Establishing a tree shrew model of systemic lupus erythematosus and cell transplantation treatment
title Establishing a tree shrew model of systemic lupus erythematosus and cell transplantation treatment
title_full Establishing a tree shrew model of systemic lupus erythematosus and cell transplantation treatment
title_fullStr Establishing a tree shrew model of systemic lupus erythematosus and cell transplantation treatment
title_full_unstemmed Establishing a tree shrew model of systemic lupus erythematosus and cell transplantation treatment
title_short Establishing a tree shrew model of systemic lupus erythematosus and cell transplantation treatment
title_sort establishing a tree shrew model of systemic lupus erythematosus and cell transplantation treatment
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995612/
https://www.ncbi.nlm.nih.gov/pubmed/27558022
http://dx.doi.org/10.1186/s13287-016-0385-1
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