Reduced Nurr1 expression increases the vulnerability of mesencephalic dopamine neurons to MPTP-induced injury

Author(s): Le W, Conneely OM, He Y, Jankovic J, Appel SH

Abstract

Mutation in the Nurr1 gene, a member of the nuclear receptor superfamily, causes selective agenesis of dopaminergic neurons in the midbrain of null mice. Homozygous Nurr1 knockout mice (Nurr1-/-) die 1 day after birth, but heterozygous mice (Nurr1 +/-) survive postnatally without obvious locomotor deficits. Although adult Nurr1 +/- mice show significantly reduced Nurr1 protein levels in the substantia nigra (SN), they display a normal range of tyrosine hydroxylase-positive neuron numbers in the SN and normal levels of dopamine in the striatum. The reduction in Nurr1 expression in Nurr1 +/- mice, however, confers increased vulnerability to the selective dopaminergic neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) compared with wild-type (Nurr1 +/+) mice. This study suggests that Nurr1 may play an important role in maintaining mature mesencephalic dopaminergic neuron function and that a defect in Nurr1 may increase susceptibility to SN injury.

Similar Articles

Etiology of Parkinson's disease: Genetics and environment revisited

Author(s): Steece-Collier K, Maries E, Kordower JH

Dopamine neuron agenesis in Nurr1-deficient mice

Author(s): Zetterström RH, Solomin L, Jansson L, Hoffer BJ, Olson L, et al.

Dopamine biosynthesis is selectively abolished in substantia nigra/ventral tegmental area but not in hypothalamic neuron

Author(s): Castillo SO, Baffi JS, Palkovits M, Goldstein DS, Kopin IJ, et al.

Nurr1 regulates dopamine synthesis and storage in MN9D dopamine cells

Author(s): Hermanson E, Joseph B, Castro D, Lindqvist E, Aarnisalo P, et al.

Transcription factor Nurr1 maintains fiber integrity and nuclearencoded mitochondrial gene expression in dopamine neurons

Author(s): Kadkhodaei B, Alvarsson A, Alvarsson A, Schintu N, Ramskold D, et al.

NR4A orphan nuclear receptors as mediators of CREB-dependent neuroprotection

Author(s): Volakakis N, Kadkhodaei B, Joodmardi E, Wallis K, Panman L, et al.

A-Synuclein-induced down-regulation of Nurr1 disrupts GDNF signaling in nigral dopamine neurons

Author(s): Decressac M, Kadkhodaei B, Mattsson B, Laguna A, Perlmann T, et al.

Combined Nurr1 and Foxa2 roles in the therapy of Parkinson’s disease

Author(s): Oh S, Chang M, Song J, Rhee Y, Joe E, et al.

Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson's disease

Author(s): Xu PY, Liang R, Jankovic J, Hunter C, Zeng YX, et al.

Familial Parkinson's disease: a hint to elucidate the mechanisms of nigral degeneration

Author(s): Hattori N, Kobayashi H, Sasaki-Hatano Y, Sato K, Mizuno Y

Mutations in NR4A2 associated with familial Parkinson disease

Author(s): Le WD, Xu P, Jankovic J, Jiang H, Appel SH, et al.

Translated mutation in the Nurr1 gene as a cause for Parkinson's disease

Author(s): Grimes DA, Han F, Panisset M, Racacho L, Xiao F, et al.

Age-related decreases in Nurr1 immunoreactivity in the human substantia nigra

Author(s): Chu Y, Kompoliti K, Cochran EJ, Mufson EJ, Kordower JH

NURR1 mutations in cases of schizophrenia and manic-depressive disorder

Author(s): BuervenichS, Carmine A, Arvidsson M, Xiang F, ZhangZ, et al.

Nurr1 enhances transcription of the human dopamine transporter gene through a novel mechanism

Author(s): Sacchetti P, Mitchell TR, Granneman JG, Bannon MJ

Regulation of GTP cyclohydrolase I expression by orphan receptor Nurr1 in cell culture and in vivo

Author(s): Gil M, McKinney C, Lee MK, Eells JB, Phyillaier MA, et al.

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

Author(s): Kadkhodaei B, Ito T, Joodmardi E,Mattsson B, Rouillard C, et al.

Nitric oxide mediates increased susceptibility to dopaminergic damage in Nurr1 heterozygous mice

Author(s): Imam SZ, Jankovic J, Ali SF, Skinner JT, Xie W, et al.

Aging of the striatum: mechanisms and interventions

Author(s): Umegaki H, Roth GS, Ingram DK

Structure and function of the Nur77 subfamily, a unique class of hormone nuclear receptors

Author(s): Eells JB,Witta J,Otridge JB, Zuffova E, Nikodem VM

Age-dependent dopaminergic dysfunction in Nurr1 knockout mice

Author(s): Iang C, Wan X, He Y, Pan T, Jankovic J, et al.

Chronic Toxoplasma gondii in Nurr1-null heterozygous mice exacerbates elevated

Author(s): EellJB, Varela-Stokes A, Guo-Ross SX, Kummari E, Smith HM, et al.

Parkinson disease in twins: an etiologic study

Author(s): Tanner CM, Ottman R, Goldman SM, Ellenberg J, Chan P, et al.

No evidence for heritability of Parkinson disease in Swedish twins

Author(s): Wirdefeldt K, Gatz M, Schalling M, Pedersen NL

Heritability of Parkinson disease in Swedish twins: a longitudinal study

Author(s): Wirdefeldt K, Gatz M, Reynolds CA, Prescott CA, Pedersen NL

Decreased ethanol preferences and wheel running in Nurr1-deficient mice

Author(s): Werme M, HermansonE, Carmine A, Buervenich S, Zetterstrom RH, et al.

Schizophrenia-relevant behaviors in a genetic mouse model of constitutive Nurr1 deficiency

Author(s): VuillermotS, JoodmardiE, Perlmann T, Ove Ögren S,FeldonJ, et al.

Otx2 expression is restricted to dopaminergic neurons of the ventral tegmental area in the adult brain

Author(s): DiSalvio M, Di Giovannantonio LG, OmodeiD, AcamporaD, SimeoneA