Literature DB >> 23681617

Preparation of primary cultured dopaminergic neurons from mouse brain.

Won-Seok Choi1, Hyung-Wook Kim, Zhengui Xia.   

Abstract

Dopaminergic neurons are involved in a variety of normal brain functions; degenerations of these neurons cause diseases in human. Investigation of how dopaminergic neurons respond to extracellular signals and molecular mechanisms regulating dopaminergic neuron survival and death often requires reliable, reproducible, and high-quality primary cultures of dopaminergic neurons. Here, we described methods to dissect and culture these neurons from embryonic mesencephalon of mouse brain. We utilize coverslips made from Aclar film to maximize the number of surviving dopaminergic neuron in the culture and immunocytochemistry of tyrosine hydroxylase (TH) to identify dopaminergic neuron.

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Year:  2013        PMID: 23681617     DOI: 10.1007/978-1-62703-444-9_6

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  4 in total

Review 1.  Model systems for analysis of dopamine transporter function and regulation.

Authors:  Moriah J Hovde; Garret H Larson; Roxanne A Vaughan; James D Foster
Journal:  Neurochem Int       Date:  2018-09-01       Impact factor: 3.921

2.  Cell-attached and Whole-cell Patch-clamp Recordings of Dopamine Neurons in the Substantia Nigra Pars Compacta of Mouse Brain Slices.

Authors:  Stefano Cattaneo; Maria Regoni; Jenny Sassone; Stefano Taverna
Journal:  Bio Protoc       Date:  2021-08-05

3.  JNK inhibition of VMAT2 contributes to rotenone-induced oxidative stress and dopamine neuron death.

Authors:  Won-Seok Choi; Hyung-Wook Kim; Zhengui Xia
Journal:  Toxicology       Date:  2014-12-09       Impact factor: 4.221

4.  Comparison of Rat Primary Midbrain Neurons Cultured in DMEM/F12 and Neurobasal Mediums.

Authors:  Neda Valian; Mansooreh Heravi; Abolhassan Ahmadiani; Leila Dargahi
Journal:  Basic Clin Neurosci       Date:  2021-03-01
  4 in total

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