Nurr1, an orphan receptor of the nuclear receptor superfamily, is widely ex
pressed in the central nervous system (CNS) including brain regions where d
opaminergic neurons are abundant. Recent analyses of Nurr1 null mutant mice
have shown that Nurr1 is essential for the development and survival of mid
brain dopaminergic neurons. However, other dopaminergic neuronal population
s do not seem to be affected by ablation of the Nurr1 gene. The purpose of
the present study was to investigate the degree of co-existence of Nurr1 mR
NA and tyrosine hydroxylase (TH) immunoreactivity in the brain of adult mic
e to better characterize the selective effects of Nurr1 on catecholaminergi
c neurons. Our results indicate that the majority of TH-immunoreactive neur
ons in the substantia nigra (SN; 96%), ventral tegmental area (VTA; 95%), r
etrorubral field (91%), olfactory bulb (85%), linear nucleus raphe (91%) an
d central grey (61%) express Nurr1, In contrast, dopaminergic cells of the
paraventricular and periventricular hypothalamic nucleus showed only a few
Nurr1/TH double labeled neurons, while TH-immunoreactive neurons in the arc
uate nucleus and zona incerta did not express Nurr1 mRNA. Nurr1 expression
was also excluded from (nor)adrenergic neurons of the brainstem. In conclus
ion, Nurr1 transcripts were not found in all CNS catecholaminergic neurons.
Nurr1 expression was confined to periglomerular and midbrain dopaminergic
neurons. These results suggest that within the adult mouse brain, Nurr1 may
participate in dopaminergic functions of the olfactory bulb and midbrain.
(C) 1999 Elsevier Science B.V. All rights reserved.