Stress and glucocorticoid regulation of NR4A genes in mice.

Jean-Christophe Helbling, Amandine M. Minni, Véronique Pallet, Marie-Pierre Moisan
Journal of Neuroscience Research. 2014-02-19; 92(7): 825-834
DOI: 10.1002/jnr.23366

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The NR4A nuclear receptors subgroup, comprising Nur77 (NR4A1), Nurr1 (NR4A2), and
Nor1 (NR4A3), are orphan receptors induced by a variety of signals, including
stress. These receptors are described as early response genes and in vitro
studies have shown that they take part in regulation of the
hypothalamic-pituitary-adrenal (HPA) axis, the major stress-responsive
neuroendocrine system. This study analyzes further the interweaving of NR4A
receptors with the HPA axis at rest and after a restraint stress in vivo in mice.
We show that each NR4A member has a similar mRNA expression pattern and low
levels of expression at rest except, in particular in hippocampus for Nurr1 and
in adrenals for Nur77. After restraint stress, mRNA expression of each NR4A is
markedly induced in adrenals and pituitary and significantly in hypothalamus. In
higher cerebral regions, such as cortex, hippocampus, and amygdala, induction of
NR4A mRNA elicited by stress was very moderate or undetected. The influence of
glucocorticoids on NR4A mRNA expression was analyzed by comparing wild-type and
Cbg k.o. mice used as a model of glucocorticoid hyposignaling. Nur77 mRNA and
protein expression and a downstream Nur77 target gene were found to be affected
in the hypothalamus and pituitary of the Cbg k.o. mice but not in hippocampus and
cortex. These results further support a physiological role of NR4A orphan
receptors in the glucocorticoid response to stress.


Auteurs Bordeaux Neurocampus