Accéder au contenu
Merck

Clock genes control cortical critical period timing.

Neuron (2015-03-25)
Yohei Kobayashi, Zhanlei Ye, Takao K Hensch
RÉSUMÉ

Circadian rhythms control a variety of physiological processes, but whether they may also time brain development remains largely unknown. Here, we show that circadian clock genes control the onset of critical period plasticity in the neocortex. Within visual cortex of Clock-deficient mice, the emergence of circadian gene expression was dampened, and the maturation of inhibitory parvalbumin (PV) cell networks slowed. Loss of visual acuity in response to brief monocular deprivation was concomitantly delayed and rescued by direct enhancement of GABAergic transmission. Conditional deletion of Clock or Bmal1 only within PV cells recapitulated the results of total Clock-deficient mice. Unique downstream gene sets controlling synaptic events and cellular homeostasis for proper maturation and maintenance were found to be mis-regulated by Clock deletion specifically within PV cells. These data demonstrate a developmental role for circadian clock genes outside the suprachiasmatic nucleus, which may contribute mis-timed brain plasticity in associated mental disorders.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
Anticorps anti-NeuN, clone A60, clone A60, Chemicon®, from mouse
Sigma-Aldrich
Anticorps anti-somatostatine, clone YC7, culture supernatant, clone YC7, Chemicon®
Sigma-Aldrich
Anticorps anti-recombinase Cre, clone 2D8, ascites fluid, clone 2D8, Chemicon®
Sigma-Aldrich
Anticorps anti-mPER1 (résidus 6-21), serum, from rabbit
Sigma-Aldrich
Anti-BMAL1 Antibody, serum, from guinea pig
Sigma-Aldrich
Anti-CLOCK Antibody, serum, Chemicon®