Cargando…
Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment
BACKGROUND: The present study was conducted to evaluate the distribution of Wharton’s jelly-derived mesenchymal stem cells (WJMSCs) and their repairing function on the oviduct. METHODS: WJMSCs were transfected with the LV3-GFP-PURO lentivirus. Female New Zealand rabbits (n = 24) were divided randoml...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709981/ https://www.ncbi.nlm.nih.gov/pubmed/29191249 http://dx.doi.org/10.1186/s13287-017-0714-z |
_version_ | 1783282890975477760 |
---|---|
author | Li, Zhe Zhang, Zhao Ming, Wai-kit Chen, Xin Xiao, Xiao-min |
author_facet | Li, Zhe Zhang, Zhao Ming, Wai-kit Chen, Xin Xiao, Xiao-min |
author_sort | Li, Zhe |
collection | PubMed |
description | BACKGROUND: The present study was conducted to evaluate the distribution of Wharton’s jelly-derived mesenchymal stem cells (WJMSCs) and their repairing function on the oviduct. METHODS: WJMSCs were transfected with the LV3-GFP-PURO lentivirus. Female New Zealand rabbits (n = 24) were divided randomly into control A and B groups and experimental C and D groups to establish inflammation models. Sterile saline solution or WJMSCs were injected into rabbits via ear veins and/or genital tract perfusion once weekly for 3 weeks. All rabbits were humanely sacrificed 1 week after the last perfusion to collect the oviduct, uterus, liver, and bladder for examination. Green fluorescent protein (GFP) and cytokeratin 7 (CK7) were imaged using a Leica Qwin Plus V3 fluorescence confocal microscope and analyzed as mean optical densities in an Image-Pro Plus analysis system. RESULTS: We found that lentivirus expressing the GFP gene produced an efficient transfection. The mean optical density values of GFP and CK7 in the oviducts were higher in the experimental D group than those in the control A and experimental C groups. No GFP fluorescence deposits occurred in the bladder of the control A group or experimental C group. Colocalization of CK7 and WJMSCs was observed in the oviducts in all groups. CONCLUSIONS: WJMSCs exhibited homing characteristics and migrated to the injured oviduct to promote epithelial cell growth. Additionally, local treatment resulted in higher efficiency. |
format | Online Article Text |
id | pubmed-5709981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57099812017-12-06 Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment Li, Zhe Zhang, Zhao Ming, Wai-kit Chen, Xin Xiao, Xiao-min Stem Cell Res Ther Research BACKGROUND: The present study was conducted to evaluate the distribution of Wharton’s jelly-derived mesenchymal stem cells (WJMSCs) and their repairing function on the oviduct. METHODS: WJMSCs were transfected with the LV3-GFP-PURO lentivirus. Female New Zealand rabbits (n = 24) were divided randomly into control A and B groups and experimental C and D groups to establish inflammation models. Sterile saline solution or WJMSCs were injected into rabbits via ear veins and/or genital tract perfusion once weekly for 3 weeks. All rabbits were humanely sacrificed 1 week after the last perfusion to collect the oviduct, uterus, liver, and bladder for examination. Green fluorescent protein (GFP) and cytokeratin 7 (CK7) were imaged using a Leica Qwin Plus V3 fluorescence confocal microscope and analyzed as mean optical densities in an Image-Pro Plus analysis system. RESULTS: We found that lentivirus expressing the GFP gene produced an efficient transfection. The mean optical density values of GFP and CK7 in the oviducts were higher in the experimental D group than those in the control A and experimental C groups. No GFP fluorescence deposits occurred in the bladder of the control A group or experimental C group. Colocalization of CK7 and WJMSCs was observed in the oviducts in all groups. CONCLUSIONS: WJMSCs exhibited homing characteristics and migrated to the injured oviduct to promote epithelial cell growth. Additionally, local treatment resulted in higher efficiency. BioMed Central 2017-12-01 /pmc/articles/PMC5709981/ /pubmed/29191249 http://dx.doi.org/10.1186/s13287-017-0714-z Text en © The Author(s). 2017 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 Li, Zhe Zhang, Zhao Ming, Wai-kit Chen, Xin Xiao, Xiao-min Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment |
title | Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment |
title_full | Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment |
title_fullStr | Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment |
title_full_unstemmed | Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment |
title_short | Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment |
title_sort | tracing gfp-labeled wjmscs in vivo using a chronic salpingitis model: an animal experiment |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709981/ https://www.ncbi.nlm.nih.gov/pubmed/29191249 http://dx.doi.org/10.1186/s13287-017-0714-z |
work_keys_str_mv | AT lizhe tracinggfplabeledwjmscsinvivousingachronicsalpingitismodelananimalexperiment AT zhangzhao tracinggfplabeledwjmscsinvivousingachronicsalpingitismodelananimalexperiment AT mingwaikit tracinggfplabeledwjmscsinvivousingachronicsalpingitismodelananimalexperiment AT chenxin tracinggfplabeledwjmscsinvivousingachronicsalpingitismodelananimalexperiment AT xiaoxiaomin tracinggfplabeledwjmscsinvivousingachronicsalpingitismodelananimalexperiment |