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Neuronal medium that supports basic synaptic functions and activity of human neurons in vitro

Authors :
Bardy, C.
Hurk, M. van den
Eames, T.
Marchand, C.
Hernandez, R.V.
Kellogg, M.
Gorris, M.A.J.
Galet, B.
Palomares, V.
Brown, J.
Bang, A.G.
Mertens, J.
Bohnke, L.
Boyer, L.
Simon, S.
Gage, F.H.
Bardy, C.
Hurk, M. van den
Eames, T.
Marchand, C.
Hernandez, R.V.
Kellogg, M.
Gorris, M.A.J.
Galet, B.
Palomares, V.
Brown, J.
Bang, A.G.
Mertens, J.
Bohnke, L.
Boyer, L.
Simon, S.
Gage, F.H.
Source :
Proceedings of the National Academy of Sciences USA; E2725; 34; 0027-8424; 20; 112; ~Proceedings of the National Academy of Sciences USA~E2725~34~~~0027-8424~20~112~~
Publication Year :
2015

Abstract

Item does not contain fulltext<br />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.

Details

Database :
OAIster
Journal :
Proceedings of the National Academy of Sciences USA; E2725; 34; 0027-8424; 20; 112; ~Proceedings of the National Academy of Sciences USA~E2725~34~~~0027-8424~20~112~~
Publication Type :
Electronic Resource
Accession number :
edsoai.on1284163121
Document Type :
Electronic Resource