Time-Course of Changes in Phosphorylated CREB in Neuroblasts and BDNF in the Mouse Dentate Gyrus at Early Postnatal Stages |
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| Authors: | In Koo Hwang Ki-Yeon Yoo Dae Young Yoo Ji Won Choi Choong Hyun Lee Jung Hoon Choi Yeo Sung Yoon Moo-Ho Won |
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| Institution: | (1) Department of Anatomy and Cell Biology, College of Veterinary Medicine, and Research Institute for Veterinary Science, Seoul National University, Seoul, 151-742, South Korea;(2) Department of Oral Anatomy, College of Dentistry, Gangneung-Wonju National University, Gangneung, 210-702, South Korea;(3) Laboratory of Veterinary Pharmacology, College of Veterinary Medicine, Seoul National University, Seoul, 151-742, South Korea;(4) Department of Neurobiology, School of Medicine, Kangwon National University, Chuncheon, 200-701, South Korea;(5) Department of Anatomy, College of Veterinary Medicine, Kangwon National University, Chuncheon, 200-701, South Korea; |
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| Abstract: | Cyclic AMP (cAMP) response element-binding protein (CREB) is involved in memory, learning, and synaptic transmission. In this
study, we observed changes of phosphorylated CREB (pCREB) immunoreactivity and its protein levels as well as brain-derived
neurotrophic factor (BDNF) levels in the hippocampal dentate gyrus at postnatal (P) 1, 7, 14, and 21 in mice. In addition,
we also investigated pCREB expression in doublecortin (DCX, a marker for neuronal progenitors) immunoreactive neuroblasts
at P21. pCREB immunoreaction at P1 was detected in most of cells in the dentate gyrus, thereafter pCREB immunoreactivity was
decreased in all the layers of the dentate gyrus with time, however, strong pCREB immunoreactivity was shown in cells confined
to the subgranular zone of the dentate gyrus at P21. In this group, many pCREB immunoreactive cells were co-localized with
DCX immunoreactive neuroblasts. In addition, pCREB protein levels were decreased with age, showing that their levels were
very low at P21, while BDNF protein levels were increased with age. These results suggest that pCREB may play important roles
in functional maturity of granule cells in mice. |
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