Optimization of glioblastoma multiforme stem cell isolation, transfection, and transduction.

Publication Type	Academic Article
Authors	Gürsel D, Beyene R, Hofstetter C, Greenfield J, Souweidane M, Kaplitt M, Arango-Lievano M, Howard B, Boockvar J
Journal	J Neurooncol
Volume	104
Issue	2
Pagination	509-22
Date Published	02/19/2011
ISSN	1573-7373
Keywords	Brain Neoplasms, Cell Separation, Glioblastoma, Neoplastic Stem Cells
Abstract	It has been postulated that brain tumor stem cells (TSCs) may be the population of cells responsible for the maintenance and recurrence of glioblastoma multiforme (GBM). The purpose of this study was to optimize a reproducible protocol for generating TSCs for their subsequent transfection or transduction. Patient GBMs were enzymatically and mechanically dissociated and tumor spheres were resuspended in appropriate media and analyzed to ensure they met stem cell criteria. These cells were then transfected with a plasmid or transduced with a viral vector to introduce a previously absent gene and then allowed to form tumor spheres. Tumor spheres were generated from patient GBMs without contamination. These cells met stringent criteria as stem cells, including multipotentiality and self-renewal. High efficiency transfection and transduction of tumor spheres was possible, even at the core of the sphere. This allowed for the introduction of new genes to the TSCs, as evidenced by fluorescent microscopy and Western blot analysis. This study is a guide to optimize the generation of patient derived GBM tumor spheres without RBC and dead cell contamination. GBM TSCs within tumor spheres can easily be transfected with plasmids or transduced with a virus. This is important from a therapeutic perspective if gene replacement is to be successful in replacing genes lost in GBM progression or to knock down or silence genes that are over-expressed in malignant brain tumors.
DOI	10.1007/s11060-011-0528-2
PubMed ID	21336775