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Generation of cortical neurons from mouse embryonic stem cells.

Nature protocols (2009-10-03)
Nicolas Gaspard, Tristan Bouschet, Adèle Herpoel, Gilles Naeije, Jelle van den Ameele, Pierre Vanderhaeghen
ABSTRACT

Embryonic stem cells (ESCs) constitute a tool of great potential in neurobiology, enabling the directed differentiation of specific neural cell types. We have shown recently that neurons of the cerebral cortex can be generated from mouse ESCs cultured in a chemically defined medium that contains no morphogen, but in the presence of the sonic hedgehog inhibitor cyclopamine. Corticogenesis from ESCs recapitulates the most important steps of cortical development, leading to the generation of multipotent cortical progenitors that sequentially produce cortical pyramidal neurons displaying distinct layer-specific identities. The protocol provides a most reductionist cellular model to tackle the complex mechanisms of cortical development and function, thereby opening new perspectives for the modeling of cortical diseases and the design of novel neurological treatments, while offering an alternative to animal use. In this protocol, we describe a method by which millions of cortical neurons can be generated in 2-3 weeks, starting from a single frozen vial of ESCs.

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Sigma-Aldrich
Anticorpo anti-colina acetiltransferasi, Chemicon®, from goat
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Gelatin from bovine skin, Type B, powder, BioReagent, suitable for cell culture
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Proteina LIF ricombinante di topo ESGRO®, ESGRO Leukemia Inhibitory Factor (LIF) supplement for mouse ES cell culture. Each vial contains 10^7 units/ml.
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Anticorpo anti-tirosina idrossilasi, clone LNC1, ascites fluid, clone LNC1, Chemicon®
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Cyclopamine, V. californicum, Cyclopamine, V. californicum, CAS 4449-51-8, is a cell-permeable steroidal alkaloid & cholesterol mimic that specifically antagonizes Sonic Hedgehog signaling through direct interaction with Smo.