Extraction and purification of tumorigenic Schwann cells in vitro from neurofibromatosis type 2 tissues

Objective To establish a simple method to extract and purify tumorigenic Schwann cells (TSCs) from neurofibromatosis type 2 (NF2) tumor tissues in vitro, in order to improve the successful rate of primary culture and obtain a large number of TSCs from NF2 patients for further study. Methods Six fres...

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Main Authors: Wei WANG, Xuejun YANG, Yu LI, Xuetao DONG, Huamin WANG, Haolang MING, Bin ZHANG, Shengping YU
Format: Article
Language:English
Published: Tianjin Huanhu Hospital 2011-02-01
Series:Chinese Journal of Contemporary Neurology and Neurosurgery
Subjects:
Online Access:http://www.cjcnn.org/index.php/cjcnn/article/view/319
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spelling doaj-de691f6843ba4663b74a9bdaae139d7d2020-11-24T22:22:42ZengTianjin Huanhu HospitalChinese Journal of Contemporary Neurology and Neurosurgery1672-67312011-02-011118287318Extraction and purification of tumorigenic Schwann cells in vitro from neurofibromatosis type 2 tissuesWei WANGXuejun YANGYu LIXuetao DONGHuamin WANGHaolang MINGBin ZHANGShengping YUObjective To establish a simple method to extract and purify tumorigenic Schwann cells (TSCs) from neurofibromatosis type 2 (NF2) tumor tissues in vitro, in order to improve the successful rate of primary culture and obtain a large number of TSCs from NF2 patients for further study. Methods Six fresh tumor tissues from patients with NF2 were obtained from 2009 to 2010 in our hospital. TSCs were extracted after collagenase digestion, followed by cell purification through rapid digestion with low trypsin concentration, differential detachment and clone screening. Morphological changes of TSCs were observed under inverted microscope and cultured TSCs were identified immunocytochemically by S ⁃ 100 protein staining. Results TSCs were successfully cultured from 3 NF2 specimens. A large number of bipolar spindle or triangular⁃shaped cells could be seen on the third day of primary culture and 4 to 5 clones were formed after the third passage in each successfully cultured specimen. Purified TSCs expressed S ⁃ 100 protein detected by immunocytochemistry with the rate of positive cells of above 95%, and their cell activity was fine and were able to be passaged stably in the subculture. Conclusion It is a successful culture method to extract and purify TSCs, combining primary culture with rapid trypsin digestion with low concentration and differential detachment. After clone screening, the purified and energetic TSCs can be obtained and applied to clinical study for NF2 pathogenesis and treatment. Fibroblasts (FBs) can be removed effectively as well. DOI:10.3969/j.issn.1672-6731.2011.01.017http://www.cjcnn.org/index.php/cjcnn/article/view/319Neurofibromatosis 2Schwann cellsCells, culturedImmunohistochemistry
collection DOAJ
language English
format Article
sources DOAJ
author Wei WANG
Xuejun YANG
Yu LI
Xuetao DONG
Huamin WANG
Haolang MING
Bin ZHANG
Shengping YU
spellingShingle Wei WANG
Xuejun YANG
Yu LI
Xuetao DONG
Huamin WANG
Haolang MING
Bin ZHANG
Shengping YU
Extraction and purification of tumorigenic Schwann cells in vitro from neurofibromatosis type 2 tissues
Chinese Journal of Contemporary Neurology and Neurosurgery
Neurofibromatosis 2
Schwann cells
Cells, cultured
Immunohistochemistry
author_facet Wei WANG
Xuejun YANG
Yu LI
Xuetao DONG
Huamin WANG
Haolang MING
Bin ZHANG
Shengping YU
author_sort Wei WANG
title Extraction and purification of tumorigenic Schwann cells in vitro from neurofibromatosis type 2 tissues
title_short Extraction and purification of tumorigenic Schwann cells in vitro from neurofibromatosis type 2 tissues
title_full Extraction and purification of tumorigenic Schwann cells in vitro from neurofibromatosis type 2 tissues
title_fullStr Extraction and purification of tumorigenic Schwann cells in vitro from neurofibromatosis type 2 tissues
title_full_unstemmed Extraction and purification of tumorigenic Schwann cells in vitro from neurofibromatosis type 2 tissues
title_sort extraction and purification of tumorigenic schwann cells in vitro from neurofibromatosis type 2 tissues
publisher Tianjin Huanhu Hospital
series Chinese Journal of Contemporary Neurology and Neurosurgery
issn 1672-6731
publishDate 2011-02-01
description Objective To establish a simple method to extract and purify tumorigenic Schwann cells (TSCs) from neurofibromatosis type 2 (NF2) tumor tissues in vitro, in order to improve the successful rate of primary culture and obtain a large number of TSCs from NF2 patients for further study. Methods Six fresh tumor tissues from patients with NF2 were obtained from 2009 to 2010 in our hospital. TSCs were extracted after collagenase digestion, followed by cell purification through rapid digestion with low trypsin concentration, differential detachment and clone screening. Morphological changes of TSCs were observed under inverted microscope and cultured TSCs were identified immunocytochemically by S ⁃ 100 protein staining. Results TSCs were successfully cultured from 3 NF2 specimens. A large number of bipolar spindle or triangular⁃shaped cells could be seen on the third day of primary culture and 4 to 5 clones were formed after the third passage in each successfully cultured specimen. Purified TSCs expressed S ⁃ 100 protein detected by immunocytochemistry with the rate of positive cells of above 95%, and their cell activity was fine and were able to be passaged stably in the subculture. Conclusion It is a successful culture method to extract and purify TSCs, combining primary culture with rapid trypsin digestion with low concentration and differential detachment. After clone screening, the purified and energetic TSCs can be obtained and applied to clinical study for NF2 pathogenesis and treatment. Fibroblasts (FBs) can be removed effectively as well. DOI:10.3969/j.issn.1672-6731.2011.01.017
topic Neurofibromatosis 2
Schwann cells
Cells, cultured
Immunohistochemistry
url http://www.cjcnn.org/index.php/cjcnn/article/view/319
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