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Use of Granulocyte Colony-Stimulating Factor for the Treatment of Thin Endometrium in Experimental Rats
Granulocyte colony-stimulating factor (G-CSF) induces stem cells to mobilize to the injury site, which have beneficial effect on tissue repair. The aim of this study was to investigate the effect of G-CSF on the thin endometrium in rat models. In the present study, rats with thin endometrium were di...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871160/ https://www.ncbi.nlm.nih.gov/pubmed/24376532 http://dx.doi.org/10.1371/journal.pone.0082375 |
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author | Zhao, Jing Tian, Tian Zhang, Qiong Wang, Yonggang Li, Yanping |
author_facet | Zhao, Jing Tian, Tian Zhang, Qiong Wang, Yonggang Li, Yanping |
author_sort | Zhao, Jing |
collection | PubMed |
description | Granulocyte colony-stimulating factor (G-CSF) induces stem cells to mobilize to the injury site, which have beneficial effect on tissue repair. The aim of this study was to investigate the effect of G-CSF on the thin endometrium in rat models. In the present study, rats with thin endometrium were divided into 4 groups (experimental group I: administrated with G-CSF (40 µg/kg/d) 4–6 hours post-modeling; control group I: administrated with saline 4–6 hours post-modeling; experimental group II: administrated with G-CSF (40 µg/kg/d) 12 days post-modeling; control group II: administrated with saline 12 days post-modeling. The agentia was given once daily and last for 5 days. Endometrial morphology was analyzed by Hematoxylin-Eosin staining, and the regeneration of endometrial cells was evaluated by immunohistochemistry and western-blot with cytokeratin and vimentin. We found that endometrial thickness and morphology presented a significant difference between experimental groups and control groups. No matter when we start with G-CSF, there was a significantly thicker endometrium and stronger expression of cytokeratin/vimintin in the experimental groups compared with the control groups (P<0.01). There were significant thicker endometrial lining and stronger expression of cytokeratin/vimintin in experimental group I than that of experimental group II (P<0.05), but there was no difference in the endometrial lining and the expression of cytokeratin/vimintin between the two control groups (P>0.05). In conclusion, G-CSF can promote the regeneration of endometrial cells in animal research, especially when the G-CSF was administrated earlier. |
format | Online Article Text |
id | pubmed-3871160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38711602013-12-27 Use of Granulocyte Colony-Stimulating Factor for the Treatment of Thin Endometrium in Experimental Rats Zhao, Jing Tian, Tian Zhang, Qiong Wang, Yonggang Li, Yanping PLoS One Research Article Granulocyte colony-stimulating factor (G-CSF) induces stem cells to mobilize to the injury site, which have beneficial effect on tissue repair. The aim of this study was to investigate the effect of G-CSF on the thin endometrium in rat models. In the present study, rats with thin endometrium were divided into 4 groups (experimental group I: administrated with G-CSF (40 µg/kg/d) 4–6 hours post-modeling; control group I: administrated with saline 4–6 hours post-modeling; experimental group II: administrated with G-CSF (40 µg/kg/d) 12 days post-modeling; control group II: administrated with saline 12 days post-modeling. The agentia was given once daily and last for 5 days. Endometrial morphology was analyzed by Hematoxylin-Eosin staining, and the regeneration of endometrial cells was evaluated by immunohistochemistry and western-blot with cytokeratin and vimentin. We found that endometrial thickness and morphology presented a significant difference between experimental groups and control groups. No matter when we start with G-CSF, there was a significantly thicker endometrium and stronger expression of cytokeratin/vimintin in the experimental groups compared with the control groups (P<0.01). There were significant thicker endometrial lining and stronger expression of cytokeratin/vimintin in experimental group I than that of experimental group II (P<0.05), but there was no difference in the endometrial lining and the expression of cytokeratin/vimintin between the two control groups (P>0.05). In conclusion, G-CSF can promote the regeneration of endometrial cells in animal research, especially when the G-CSF was administrated earlier. Public Library of Science 2013-12-23 /pmc/articles/PMC3871160/ /pubmed/24376532 http://dx.doi.org/10.1371/journal.pone.0082375 Text en © 2013 Zhao et al http://creativecommons.org/licenses/by/4.0/ Except for Figure 3, 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 author and source are credited. |
spellingShingle | Research Article Zhao, Jing Tian, Tian Zhang, Qiong Wang, Yonggang Li, Yanping Use of Granulocyte Colony-Stimulating Factor for the Treatment of Thin Endometrium in Experimental Rats |
title | Use of Granulocyte Colony-Stimulating Factor for the Treatment of Thin Endometrium in Experimental Rats |
title_full | Use of Granulocyte Colony-Stimulating Factor for the Treatment of Thin Endometrium in Experimental Rats |
title_fullStr | Use of Granulocyte Colony-Stimulating Factor for the Treatment of Thin Endometrium in Experimental Rats |
title_full_unstemmed | Use of Granulocyte Colony-Stimulating Factor for the Treatment of Thin Endometrium in Experimental Rats |
title_short | Use of Granulocyte Colony-Stimulating Factor for the Treatment of Thin Endometrium in Experimental Rats |
title_sort | use of granulocyte colony-stimulating factor for the treatment of thin endometrium in experimental rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871160/ https://www.ncbi.nlm.nih.gov/pubmed/24376532 http://dx.doi.org/10.1371/journal.pone.0082375 |
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