| Literature DB >> 25870293 |
Cedric Bardy1, Mark van den Hurk2, Tameji Eames3, Cynthia Marchand4, Ruben V Hernandez3, Mariko Kellogg3, Mark Gorris3, Ben Galet3, Vanessa Palomares3, Joshua Brown5, Anne G Bang5, Jerome Mertens3, Lena Böhnke3, Leah Boyer3, Suzanne Simon3, Fred H Gage1.
Abstract
Human cell reprogramming technologies offer access to live human neurons from patients and provide a new alternative for modeling neurological disorders in vitro. Neural electrical activity is the essence of nervous system function in vivo. Therefore, we examined neuronal activity in media widely used to culture neurons. We found that classic basal media, as well as serum, impair action potential generation and synaptic communication. To overcome this problem, we designed a new neuronal medium (BrainPhys basal + serum-free supplements) in which we adjusted the concentrations of inorganic salts, neuroactive amino acids, and energetic substrates. We then tested that this medium adequately supports neuronal activity and survival of human neurons in culture. Long-term exposure to this physiological medium also improved the proportion of neurons that were synaptically active. The medium was designed to culture human neurons but also proved adequate for rodent neurons. The improvement in BrainPhys basal medium to support neurophysiological activity is an important step toward reducing the gap between brain physiological conditions in vivo and neuronal models in vitro.Entities:
Keywords: BrainPhys; induced pluripotent stem cells; neurobasal DMEM; neuromedium; tissue culture milieu
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Year: 2015 PMID: 25870293 PMCID: PMC4443325 DOI: 10.1073/pnas.1504393112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205