The ability to manipulate human neural stem/precursor cells (hNSPCs) in vitro allows to investigate their utility as cell transplants for therapeutic purposes and to explore human neural development. This protocol presents a method of culturing and passaging hNSPCs in hopes of increasing reproducibility of human stem cell research.
Abstract
The ability to manipulate human neural stem/precursor cells (hNSPCs) in vitro provides a means to investigate their utility as cell transplants for therapeutic purposes as well as to explore many fundamental processes of human neural development and pathology. This protocol presents a simple method of culturing and passaging hNSPCs in hopes of standardizing this technique and increasing reproducibility of human stem cell research. The hNSPCs we use were isolated from cadaveric postnatal brain cortices by the National Human Neural Stem Cell Resource and grown as adherent cultures on flasks coated with fibronectin (Palmer et al., 2001; Schwartz et al., 2003). We culture our hNSPCs in a DMEM:F12 serum-free media supplemented with EGF, FGF, and PDGF and passage them 1:2 approximately every seven days. Using these conditions, the majority of the cells in the culture maintain a bipolar morphology and express markers of undifferentiated neural stem cells (such as nestin and sox2).
Protocol
Note: For routine culturing of our hNSPCs, we change 50-100% of the media every other day and usually passage them 1:2 once a week. The culture media contains 20% BIT-9500, 1X antibiotic/antimycotic, and growth factors (EGF, FGF, and PDGF each at 40 ng/ml) in DMEM:F12 base media. Preparing the Coated Flask and Dissociating the Cells To prepare new flasks for the passaged cells, coat T25 flasks with 10 µg/ml human fibronectin in EMEM for 4 hours, or overnight, in a 37&d…
Discussion
We have found that this protocol provides reliable cultures of hNSPCs. One critical factor for our cells is that they need to be kept as fairly dense cultures and cannot be passaged to the point that the cells are sparse. In our hands, sparse cultures grow very slowly or completely cease dividing. For this reason, we usually split our cultures 1:2 or 1:3 when a culture is extremely dense. Coating the surface of a culture dish with fibronectin is important since it promotes good cell attachment and migration, but, unl…
Acknowledgements
The authors gratefully acknowledge Dr. Philip H. Schwartz of the National Human Neural Stem Cell Resource at the Children’s Hospital, Orange County Research Institute for providing hNSPCs and initial instruction in their culturing.
Materials
Material Name
Type
Company
Catalogue Number
Comment
BIT-9500 (BSA, Insulin, Transferrin)
Reagent
Stem Cell Technologies
09500
Antibiotic-Antimycotic
Reagent
Invitrogen
15240-062
DMEM:F12 (1X)
Reagent
Invitrogen
11330-032
EMEM (1X)
Reagent
Mediatech
MT-10-010-CV
Distributed by Fisher under the indicated catalog #
Fetal Bovine Serum
Reagent
Invitrogen
10437-028
FGF, human basic recombinant
Reagent
Peprotech
100-18B
PDGF-AB
Reagent
Peprotech
100-00AB
EGF, human recombinant
Reagent
BD Biosciences
CB40052
Distributed by Fisher under the indicated catalog #
Cell Culture Flask, 25 cm2
Tool
Corning
10-126-28
Distributed by Fisher under the indicated catalog #
Fibronectin, human, natural
Reagent
BD Biosciences
CB40008A
Distributed by Fisher under the indicated catalog #
Human Neural Stem/Precursor Cells
Cells
National Human Neural Stem Cell Resource http://www.nhnscr.org/default.htm
Nethercott, H. N., Maxwell, H., Schwartz, P. H., Loring, J. F., Wesselschmidt, R. W., Schwartz, P. H. Neural stem cell culture.Human Stem Cell Manual: A Laboratory Guide. , (2007).