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The change and effect of endothelial progenitor cells in pig with multiple organ dysfunction syndromes
INTRODUCTION: The dysfunction and decrease of endothelial progenitor cells (EPCs) may play a very important role in the initiation of organ dysfunction caused by trauma or severe sepsis. We aim to measure the number and function of EPCs in the progression of multiple organ dysfunction syndromes (MOD...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750166/ https://www.ncbi.nlm.nih.gov/pubmed/19604356 http://dx.doi.org/10.1186/cc7968 |
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author | Luo, Tian Hang Wang, Yao Lu, Zheng Mao Zhou, Hong Xue, Xu Chao Bi, Jian Wei Ma, Li Ye Fang, Guo En |
author_facet | Luo, Tian Hang Wang, Yao Lu, Zheng Mao Zhou, Hong Xue, Xu Chao Bi, Jian Wei Ma, Li Ye Fang, Guo En |
author_sort | Luo, Tian Hang |
collection | PubMed |
description | INTRODUCTION: The dysfunction and decrease of endothelial progenitor cells (EPCs) may play a very important role in the initiation of organ dysfunction caused by trauma or severe sepsis. We aim to measure the number and function of EPCs in the progression of multiple organ dysfunction syndromes (MODS) caused by severe sepsis, which may help to understand the pathogenesis of MODS by the changing of EPCs. METHODS: A total of 40 pigs were randomly divided into two groups, which were subjected to hemorrhagic shock, resuscitation and endotoxemia (experimental group, n = 20) or acted as a control (control group, n = 20). The number and function of EPCs including adhesive, migratory and angiogenesis capacities were analyzed at different times in both groups. RESULTS: All the animals in the experimental group developed MODS (100%) and 17 of 20 animals (85%) died due to MODS; the incidence of MODS and death of the animals in the control group were 0% (P < 0.01). The number, migratory and adhesive capacities of EPCs decreased sharply in the animals of the experimental group corresponding to the increasing severities of MODS, but the angiogenesis function increased gradually until death. The decrease in function of EPCs preceded the decrease in number of EPCs. The decrease in number and function of EPCs occurred prior to the occurrence of MODS. CONCLUSIONS: For the first time, it was observed that the number and function of EPCs decreased sharply in the progression of MODS and that it was prior to the occurrence of MODS. The decrease in number and function of EPCs may be one of the main pathogenic factors of MODS. |
format | Text |
id | pubmed-2750166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27501662009-09-25 The change and effect of endothelial progenitor cells in pig with multiple organ dysfunction syndromes Luo, Tian Hang Wang, Yao Lu, Zheng Mao Zhou, Hong Xue, Xu Chao Bi, Jian Wei Ma, Li Ye Fang, Guo En Crit Care Research INTRODUCTION: The dysfunction and decrease of endothelial progenitor cells (EPCs) may play a very important role in the initiation of organ dysfunction caused by trauma or severe sepsis. We aim to measure the number and function of EPCs in the progression of multiple organ dysfunction syndromes (MODS) caused by severe sepsis, which may help to understand the pathogenesis of MODS by the changing of EPCs. METHODS: A total of 40 pigs were randomly divided into two groups, which were subjected to hemorrhagic shock, resuscitation and endotoxemia (experimental group, n = 20) or acted as a control (control group, n = 20). The number and function of EPCs including adhesive, migratory and angiogenesis capacities were analyzed at different times in both groups. RESULTS: All the animals in the experimental group developed MODS (100%) and 17 of 20 animals (85%) died due to MODS; the incidence of MODS and death of the animals in the control group were 0% (P < 0.01). The number, migratory and adhesive capacities of EPCs decreased sharply in the animals of the experimental group corresponding to the increasing severities of MODS, but the angiogenesis function increased gradually until death. The decrease in function of EPCs preceded the decrease in number of EPCs. The decrease in number and function of EPCs occurred prior to the occurrence of MODS. CONCLUSIONS: For the first time, it was observed that the number and function of EPCs decreased sharply in the progression of MODS and that it was prior to the occurrence of MODS. The decrease in number and function of EPCs may be one of the main pathogenic factors of MODS. BioMed Central 2009 2009-07-15 /pmc/articles/PMC2750166/ /pubmed/19604356 http://dx.doi.org/10.1186/cc7968 Text en Copyright ©2009 Luo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Luo, Tian Hang Wang, Yao Lu, Zheng Mao Zhou, Hong Xue, Xu Chao Bi, Jian Wei Ma, Li Ye Fang, Guo En The change and effect of endothelial progenitor cells in pig with multiple organ dysfunction syndromes |
title | The change and effect of endothelial progenitor cells in pig with multiple organ dysfunction syndromes |
title_full | The change and effect of endothelial progenitor cells in pig with multiple organ dysfunction syndromes |
title_fullStr | The change and effect of endothelial progenitor cells in pig with multiple organ dysfunction syndromes |
title_full_unstemmed | The change and effect of endothelial progenitor cells in pig with multiple organ dysfunction syndromes |
title_short | The change and effect of endothelial progenitor cells in pig with multiple organ dysfunction syndromes |
title_sort | change and effect of endothelial progenitor cells in pig with multiple organ dysfunction syndromes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750166/ https://www.ncbi.nlm.nih.gov/pubmed/19604356 http://dx.doi.org/10.1186/cc7968 |
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