Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we will assume that you are happy to receive all cookies and you will not see this message again. Click 'Find out more' for information on how to change your cookie settings.

A protocol for the isolation and culture of motor neurons from postnatal day 1 mouse spinal cord is described. After 72 h in culture, phase contrast microscopy reveals healthy cells with motor neuronal morphology and extensive neuritic processes. These neurons express the 75-kDa low-affinity neurotrophin receptor (p75NTR) and choline acetyltransferase (ChAT), both proteins are specifically expressed by neonatal and embryonic motor neurons in vivo. This protocol can be adapted for various postnatal motor neuron assays.

Original publication

DOI

10.1016/j.brainresprot.2003.10.001

Type

Journal article

Journal

Brain Res Brain Res Protoc

Publication Date

02/2004

Volume

12

Pages

132 - 136

Keywords

Animals, Animals, Newborn, Biomarkers, Cell Culture Techniques, Cell Differentiation, Cell Lineage, Cell Separation, Cells, Cultured, Choline O-Acetyltransferase, Immunohistochemistry, Mice, Motor Neurons, Neurites, Neurofilament Proteins, Receptor, Nerve Growth Factor, Receptors, Nerve Growth Factor, Reproducibility of Results, Spinal Cord