Polysialylated neural cell adhesion molecule modulates photic signaling in the mouse suprachiasmatic nucleus

被引:31
作者
Glass, JD [1 ]
Shena, HM
Fedorkova, L
Chen, L
Tomasiewicz, H
Watanabe, M
机构
[1] Kent State Univ, Dept Biol Sci, Kent, OH 44242 USA
[2] Emory Univ, Dept Anat & Cell Biol, Atlanta, GA 30322 USA
[3] Case Western Reserve Univ, Sch Med, Rainbow Babies & Childrens Hosp, Dept Pediat,Div Pediat Cardiol, Cleveland, OH 44106 USA
关键词
suprachiasmatic nucleus; aging; polysialic acid; neural cell adhesion molecule;
D O I
10.1016/S0304-3940(00)00786-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Polysialic acid (PSA), a sialic acid polymer that regulates plasticity and cell-cell interactions in neural tissues, is expressed in the mammalian circadian clock located in the suprachiasmatic nucleus (SCN). In vivo enzymatic removal of PSA from the mouse SCN significantly impaired both the photic induction of Fos protein in SCN cells and light-induced phase-resetting of the circadian locomotor activity rhythm. Genetic deletion of PSA and it's neural cell adhesion molecule (NCAM) carrier correspondingly attenuated light-induced circadian phase-shifting. Comparison of PSA levels between young and old mice revealed a large aging-related reduction in SCN PSA content that accompanies the diminished capacity for circadian photic response reported in old rodents. Collectively these data support the contention that PSA modulates photic signaling in the SCN, and that normal reductions in the cell surface molecule contribute to aging-related deficits in SCN circadian clock function. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:207 / 210
页数:4
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