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Pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells
BACKGROUND: This study is to explore the pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells. METHODS: CD133 positive TJ905 glioma cells were separated by immunomagnetic beads to isolate glioma stem-like cells. TJ905 cells and stem-like cells...
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/PMC4487198/ https://www.ncbi.nlm.nih.gov/pubmed/26136642 http://dx.doi.org/10.1186/s12935-015-0208-y |
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author | Jin, Feng Zhang, Ran Feng, Song Yuan, Chuan-Tao Zhang, Ren-Ya Han, Guang-Kui Li, Gen-Hua Yu, Xi-Zhen Liu, Yang Kong, Ling-Sheng Zhang, Shu-Ling Zhao, Lei |
author_facet | Jin, Feng Zhang, Ran Feng, Song Yuan, Chuan-Tao Zhang, Ren-Ya Han, Guang-Kui Li, Gen-Hua Yu, Xi-Zhen Liu, Yang Kong, Ling-Sheng Zhang, Shu-Ling Zhao, Lei |
author_sort | Jin, Feng |
collection | PubMed |
description | BACKGROUND: This study is to explore the pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells. METHODS: CD133 positive TJ905 glioma cells were separated by immunomagnetic beads to isolate glioma stem-like cells. TJ905 cells and stem-like cells were inoculated subcutaneously into the mice to establish model of transplanted tumor, respectively. Mice growing condition and behavior were observed. HE staining assay, immunohistochemical assay for GFAP, Ki-67 and Olig-2, and CD34 marked microvascular density (MVD) test were performed. RESULTS: The growing condition and behavior of mice in TJ905 stem cell group was more exaggerated and the models showed stronger malignant features pathologically than that in TJ905 cell group. Glial fibrillary acidic protein (GFAP) in TJ905 cell and stem-like cell group showed the transplanted tumor originated from astrocytes. Expression of Ki-67 and oligodendrocyte transcription factor-2 (Olig-2) in TJ905 stem cells was higher notably and CD34 expression in stem cell group was significantly higher than that in the other two groups. CONCLUSIONS: Pathological features of transplanted tumor established by CD133 positive glioblastoma stem-like cells show more malignant. Use of TJ905 stem cells to establish transplanted tumor model in nude mice is excellent for glioma research. |
format | Online Article Text |
id | pubmed-4487198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44871982015-07-02 Pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells Jin, Feng Zhang, Ran Feng, Song Yuan, Chuan-Tao Zhang, Ren-Ya Han, Guang-Kui Li, Gen-Hua Yu, Xi-Zhen Liu, Yang Kong, Ling-Sheng Zhang, Shu-Ling Zhao, Lei Cancer Cell Int Primary Research BACKGROUND: This study is to explore the pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells. METHODS: CD133 positive TJ905 glioma cells were separated by immunomagnetic beads to isolate glioma stem-like cells. TJ905 cells and stem-like cells were inoculated subcutaneously into the mice to establish model of transplanted tumor, respectively. Mice growing condition and behavior were observed. HE staining assay, immunohistochemical assay for GFAP, Ki-67 and Olig-2, and CD34 marked microvascular density (MVD) test were performed. RESULTS: The growing condition and behavior of mice in TJ905 stem cell group was more exaggerated and the models showed stronger malignant features pathologically than that in TJ905 cell group. Glial fibrillary acidic protein (GFAP) in TJ905 cell and stem-like cell group showed the transplanted tumor originated from astrocytes. Expression of Ki-67 and oligodendrocyte transcription factor-2 (Olig-2) in TJ905 stem cells was higher notably and CD34 expression in stem cell group was significantly higher than that in the other two groups. CONCLUSIONS: Pathological features of transplanted tumor established by CD133 positive glioblastoma stem-like cells show more malignant. Use of TJ905 stem cells to establish transplanted tumor model in nude mice is excellent for glioma research. BioMed Central 2015-06-13 /pmc/articles/PMC4487198/ /pubmed/26136642 http://dx.doi.org/10.1186/s12935-015-0208-y Text en © Jin et al. 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 | Primary Research Jin, Feng Zhang, Ran Feng, Song Yuan, Chuan-Tao Zhang, Ren-Ya Han, Guang-Kui Li, Gen-Hua Yu, Xi-Zhen Liu, Yang Kong, Ling-Sheng Zhang, Shu-Ling Zhao, Lei Pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells |
title | Pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells |
title_full | Pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells |
title_fullStr | Pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells |
title_full_unstemmed | Pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells |
title_short | Pathological features of transplanted tumor established by CD133 positive TJ905 glioblastoma stem-like cells |
title_sort | pathological features of transplanted tumor established by cd133 positive tj905 glioblastoma stem-like cells |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487198/ https://www.ncbi.nlm.nih.gov/pubmed/26136642 http://dx.doi.org/10.1186/s12935-015-0208-y |
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