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Lipopolysaccharide preconditioning of adipose-derived stem cells improves liver-regenerating activity of the secretome
INTRODUCTION: Growing recognition of paracrine mechanisms in stem cell plasticity has resulted in considerable interest in stem cell-derived secretome. The aim of this study was to investigate the effects of lipopolysaccharide (LPS) preconditioning on the composition and hepatic regenerative activit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416308/ https://www.ncbi.nlm.nih.gov/pubmed/25890074 http://dx.doi.org/10.1186/s13287-015-0072-7 |
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author | Lee, Sang Chul Jeong, Hye Jin Lee, Sang Kuon Kim, Say-June |
author_facet | Lee, Sang Chul Jeong, Hye Jin Lee, Sang Kuon Kim, Say-June |
author_sort | Lee, Sang Chul |
collection | PubMed |
description | INTRODUCTION: Growing recognition of paracrine mechanisms in stem cell plasticity has resulted in considerable interest in stem cell-derived secretome. The aim of this study was to investigate the effects of lipopolysaccharide (LPS) preconditioning on the composition and hepatic regenerative activity of adipose-derived stem cell (ASC) secretome. METHODS: Conditioned medium (CM) and LPS-CM were obtained after culturing human ASCs without or with low-dose LPS (0.5 ng/mL) for 24 hours. Untreated and thioacetamide-treated mouse AML12 hepatocytes were incubated for 24 hours with the control medium, LPS (0.5 ng/mL), CM, and LPS-CM and then cell viabilities were compared. CM and LPS-CM were also intravenously administered to partially hepatectomized mice, and their effects on liver regeneration were assessed by using liver weight measurements, immunohistochemistry, and Western blotting. RESULTS: In the in vitro experiments, LPS preconditioning of ASCs enhanced the mRNA expression levels of interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), hepatocyte growth factor, and vascular endothelial growth factor, which evoke inflammatory response or liver regeneration. LPS-CM significantly promoted thioacetamide-damaged AML12 cell viability compared with CM-incubated cells and the control cells (77%, 69%, and 65% P <0.05). In the in vivo experiment, LPS-CM infusion into the partially hepatectomized mice significantly reduced serum IL-6 and TNF-α levels compared with the other groups (P <0.05) on days 1 and 2 after partial hepatectomy. Moreover, LPS-CM infusion enhanced liver regeneration (based on the liver weight changes at day 7 after partial hepatectomy, 3.73% versus 3.22% in the CM group; P <0.05) and significantly reduced the elevated serum levels of aspartate transaminase and alanine transaminase (at day 1, P <0.05). CONCLUSIONS: Our results suggest that LPS preconditioning effectively stimulates ASCs to produce the secretome beneficial to hepatic regeneration. Thus, optimizing ASC secretome profile by LPS preconditioning could be a promising approach to treat liver diseases by using stem cells. |
format | Online Article Text |
id | pubmed-4416308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44163082015-05-02 Lipopolysaccharide preconditioning of adipose-derived stem cells improves liver-regenerating activity of the secretome Lee, Sang Chul Jeong, Hye Jin Lee, Sang Kuon Kim, Say-June Stem Cell Res Ther Research INTRODUCTION: Growing recognition of paracrine mechanisms in stem cell plasticity has resulted in considerable interest in stem cell-derived secretome. The aim of this study was to investigate the effects of lipopolysaccharide (LPS) preconditioning on the composition and hepatic regenerative activity of adipose-derived stem cell (ASC) secretome. METHODS: Conditioned medium (CM) and LPS-CM were obtained after culturing human ASCs without or with low-dose LPS (0.5 ng/mL) for 24 hours. Untreated and thioacetamide-treated mouse AML12 hepatocytes were incubated for 24 hours with the control medium, LPS (0.5 ng/mL), CM, and LPS-CM and then cell viabilities were compared. CM and LPS-CM were also intravenously administered to partially hepatectomized mice, and their effects on liver regeneration were assessed by using liver weight measurements, immunohistochemistry, and Western blotting. RESULTS: In the in vitro experiments, LPS preconditioning of ASCs enhanced the mRNA expression levels of interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), hepatocyte growth factor, and vascular endothelial growth factor, which evoke inflammatory response or liver regeneration. LPS-CM significantly promoted thioacetamide-damaged AML12 cell viability compared with CM-incubated cells and the control cells (77%, 69%, and 65% P <0.05). In the in vivo experiment, LPS-CM infusion into the partially hepatectomized mice significantly reduced serum IL-6 and TNF-α levels compared with the other groups (P <0.05) on days 1 and 2 after partial hepatectomy. Moreover, LPS-CM infusion enhanced liver regeneration (based on the liver weight changes at day 7 after partial hepatectomy, 3.73% versus 3.22% in the CM group; P <0.05) and significantly reduced the elevated serum levels of aspartate transaminase and alanine transaminase (at day 1, P <0.05). CONCLUSIONS: Our results suggest that LPS preconditioning effectively stimulates ASCs to produce the secretome beneficial to hepatic regeneration. Thus, optimizing ASC secretome profile by LPS preconditioning could be a promising approach to treat liver diseases by using stem cells. BioMed Central 2015-04-14 /pmc/articles/PMC4416308/ /pubmed/25890074 http://dx.doi.org/10.1186/s13287-015-0072-7 Text en © Lee et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Lee, Sang Chul Jeong, Hye Jin Lee, Sang Kuon Kim, Say-June Lipopolysaccharide preconditioning of adipose-derived stem cells improves liver-regenerating activity of the secretome |
title | Lipopolysaccharide preconditioning of adipose-derived stem cells improves liver-regenerating activity of the secretome |
title_full | Lipopolysaccharide preconditioning of adipose-derived stem cells improves liver-regenerating activity of the secretome |
title_fullStr | Lipopolysaccharide preconditioning of adipose-derived stem cells improves liver-regenerating activity of the secretome |
title_full_unstemmed | Lipopolysaccharide preconditioning of adipose-derived stem cells improves liver-regenerating activity of the secretome |
title_short | Lipopolysaccharide preconditioning of adipose-derived stem cells improves liver-regenerating activity of the secretome |
title_sort | lipopolysaccharide preconditioning of adipose-derived stem cells improves liver-regenerating activity of the secretome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416308/ https://www.ncbi.nlm.nih.gov/pubmed/25890074 http://dx.doi.org/10.1186/s13287-015-0072-7 |
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