Neural-colony forming cell assay: an assay to discriminate bona fide neural stem cells from neural progenitor cells

• Published in: Journal of visualized experiments 2011-03 (49)
• Main Authors: Azari, Hassan, Louis, Sharon A, Sharififar, Sharareh, Vedam-Mai, Vinata, Reynolds, Brent A
• Format: Article
• Language: English
• Subjects: Adult Stem Cells - cytology; Animals; Brain - cytology; Brain - embryology; Colony-Forming Units Assay - methods; Embryonic Stem Cells - cytology; Mice; Neural Stem Cells - cytology; Neuroscience
• ISSN: 1940-087X; 1940-087X
• DOI: 10.3791/2639

The neurosphere assay (NSA) is one of the most frequently used methods to isolate, expand and also calculate the frequency of neural stem cells (NSCs). Furthermore, this serum-free culture system has also been employed to expand stem cells and determine their frequency from a variety of tumors and normal tissues. It has been shown recently that a one-to-one relationship does not exist between neurosphere formation and NSCs. This suggests that the NSA as currently applied, overestimates the frequency of NSCs in a mixed population of neural precursor cells isolated from both the embryonic and adult mammalian brain. This video practically demonstrates a novel collagen based semi- solid assay, the neural-colony forming cell assay (N-CFCA), which has the ability to discriminate stem from progenitor cells based on their long-term proliferative potential, and thus provides a method to enumerate NSC frequency. In the N-CFCA, colonies ≥2 mm in diameter are derived from cells that meet all the functional criteria of a NSC, while colonies < 2mm are derived from progenitors. The N-CFCA procedure can be used for cells prepared from different sources including primary and cultured adult or embryonic mouse CNS cells. Here we use cells prepared from passage one neurospheres generated from embryonic day 14 mice brain to perform N-CFCA. The cultures are replenished with proliferation medium every seven days for three weeks to allow the plated cells to exhibit their full proliferative potential and then the frequency of neural progenitor and bona fide neural stem cells is calculated respectively by counting the number of colonies that are < 2mm and the ones that are ≥2mm in reference to the number of cells that were initially plated.