Neural subtype specification of fertilization and nuclear transfer embryonic stem cells and application in parkinsonian mice. Academic Article uri icon

Overview

abstract

  • Existing protocols for the neural differentiation of mouse embryonic stem (ES) cells require extended in vitro culture, yield variable differentiation results or are limited to the generation of selected neural subtypes. Here we provide a set of coculture conditions that allows rapid and efficient derivation of most central nervous system phenotypes. The fate of both fertilization- and nuclear transfer-derived ES (ntES) cells was directed selectively into neural stem cells, astrocytes, oligodendrocytes or neurons. Specific differentiation into gamma-aminobutyric acid (GABA), dopamine, serotonin or motor neurons was achieved by defining conditions to induce forebrain, midbrain, hindbrain and spinal cord identity. Neuronal function of ES cell-derived dopaminergic neurons was shown in vitro by electron microscopy, measurement of neurotransmitter release and intracellular recording. Furthermore, transplantation of ES and ntES cell-derived dopaminergic neurons corrected the phenotype of a mouse model of Parkinson disease, demonstrating an in vivo application of therapeutic cloning in neural disease.

publication date

  • September 21, 2003

Research

keywords

  • Coculture Techniques
  • Neurons
  • Nuclear Transfer Techniques
  • Parkinsonian Disorders
  • Stem Cell Transplantation
  • Stem Cells

Identity

Scopus Document Identifier

  • 10744229091

Digital Object Identifier (DOI)

  • 10.1038/nbt870

PubMed ID

  • 14502203

Additional Document Info

volume

  • 21

issue

  • 10