TY - JOUR
T1 - High efficacy of clonal growth and expansion of adult neural stem cells
AU - Wachs, Frank Peter
AU - Couillard-Despres, Sebastien
AU - Engelhardt, Maren
AU - Wilhelm, Daniel
AU - Ploetz, Sonja
AU - Vroemen, Maurice
AU - Kaesbauer, Johanna
AU - Uyanik, Goekhan
AU - Klucken, Jochen
AU - Karl, Claudia
AU - Tebbing, Johanna
AU - Svendsen, Clive
AU - Weidner, Norbert
AU - Kuhn, Hans Georg
AU - Winkler, Juergen
AU - Aigner, Ludwig
N1 - Funding Information:
F-PW and SC-D contributed equally to this work. This work was funded by the Volkswagen-Foundation, Hannover, and the School of Medicine, University of Regensburg, Germany (F-PW, GU, J. Klucken) (ReForM Program). SC-D and SP are funded by the Fritz-Thyssen-Foundation, Koeln, Germany. Address reprint requests to: Dr. L. Aigner, Department of Neurology, University of Regensburg, Franz-Josef-Strauss-Allee 11, D-93053 Regens-burg, Germany. E-mail: [email protected]
PY - 2003/7/1
Y1 - 2003/7/1
N2 - Neural stem cells (NSCs) from the adult central nervous system are currently being investigated for their potential use in autologous cell replacement strategies. High expansion rates of NSCs in culture are crucial for the generation of a sufficient amount of cells needed for transplantation. Here, we describe efficient growth of adult NSCs in Neurobasal medium containing B27 supplement under clonal and low-density conditions in the absence of serum or conditioned medium. Expansion of up to 15-fold within 1 week was achieved on low-density NSC cultures derived from the lateral ventricle wall, the hippocampal formation, and the spinal cord of adult rats. A 27% single-cell cloning efficiency in Neurobasal/B27 combination further demonstrates its growth-promoting ability. Multipotency and nontumorgenicity of NSCs were retained despite the high rate of culture expansion. In addition, increased cell survival was obtained when Accutase, instead of trypsin, was used for enzymatic dissociation of NSC cultures. This work provides an important step toward the development of standardized protocols for highly efficient in vitro expansion of NSCs from the adult central nervous system to move more closely to the clinical use of NSCs.
AB - Neural stem cells (NSCs) from the adult central nervous system are currently being investigated for their potential use in autologous cell replacement strategies. High expansion rates of NSCs in culture are crucial for the generation of a sufficient amount of cells needed for transplantation. Here, we describe efficient growth of adult NSCs in Neurobasal medium containing B27 supplement under clonal and low-density conditions in the absence of serum or conditioned medium. Expansion of up to 15-fold within 1 week was achieved on low-density NSC cultures derived from the lateral ventricle wall, the hippocampal formation, and the spinal cord of adult rats. A 27% single-cell cloning efficiency in Neurobasal/B27 combination further demonstrates its growth-promoting ability. Multipotency and nontumorgenicity of NSCs were retained despite the high rate of culture expansion. In addition, increased cell survival was obtained when Accutase, instead of trypsin, was used for enzymatic dissociation of NSC cultures. This work provides an important step toward the development of standardized protocols for highly efficient in vitro expansion of NSCs from the adult central nervous system to move more closely to the clinical use of NSCs.
UR - http://www.scopus.com/inward/record.url?scp=0041364517&partnerID=8YFLogxK
U2 - 10.1097/01.LAB.0000075556.74231.A5
DO - 10.1097/01.LAB.0000075556.74231.A5
M3 - Article
C2 - 12861035
AN - SCOPUS:0041364517
SN - 0023-6837
VL - 83
SP - 949
EP - 962
JO - Laboratory Investigation
JF - Laboratory Investigation
IS - 7
ER -