Literature search services are currently unavailable. During our hosting provider's UPS upgrade we experienced a hardware failure and are currently working to resolve the issue.

Preparing your results

Our searching services are busy right now. Your search will reload in five seconds.

Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Nurr1 is required for maintenance of maturing and adult midbrain dopamine neurons.

Transcription factors involved in the specification and differentiation of neurons often continue to be expressed in the adult brain, but remarkably little is known about their late functions. Nurr1, one such transcription factor, is essential for early differentiation of midbrain dopamine (mDA) neurons but continues to be expressed into adulthood. In Parkinson's disease, Nurr1 expression is diminished and mutations in the Nurr1 gene have been identified in rare cases of disease; however, the significance of these observations remains unclear. Here, a mouse strain for conditional targeting of the Nurr1 gene was generated, and Nurr1 was ablated either at late stages of mDA neuron development by crossing with mice carrying Cre under control of the dopamine transporter locus or in the adult brain by transduction of adeno-associated virus Cre-encoding vectors. Nurr1 deficiency in maturing mDA neurons resulted in rapid loss of striatal DA, loss of mDA neuron markers, and neuron degeneration. In contrast, a more slowly progressing loss of striatal DA and mDA neuron markers was observed after ablation in the adult brain. As in Parkinson's disease, neurons of the substantia nigra compacta were more vulnerable than cells in the ventral tegmental area when Nurr1 was ablated at late embryogenesis. The results show that developmental pathways play key roles for the maintenance of terminally differentiated neurons and suggest that disrupted function of Nurr1 and other developmental transcription factors may contribute to neurodegenerative disease.

Pubmed ID: 20016108


  • Kadkhodaei B
  • Ito T
  • Joodmardi E
  • Mattsson B
  • Rouillard C
  • Carta M
  • Muramatsu S
  • Sumi-Ichinose C
  • Nomura T
  • Metzger D
  • Chambon P
  • Lindqvist E
  • Larsson NG
  • Olson L
  • Bj√∂rklund A
  • Ichinose H
  • Perlmann T


The Journal of neuroscience : the official journal of the Society for Neuroscience

Publication Data

December 16, 2009

Associated Grants


Mesh Terms

  • Age Factors
  • Animals
  • Embryonic Stem Cells
  • Female
  • Gene Targeting
  • Integrases
  • Mesencephalon
  • Mice
  • Mice, Transgenic
  • Neurogenesis
  • Neurons
  • Nuclear Receptor Subfamily 4, Group A, Member 2
  • Pregnancy