HIPPOCAMPAL-NEURONS PREDISPOSED TO NEUROFIBRILLARY TANGLE FORMATION ARE ENRICHED IN TYPE-II CALCIUM CALMODULIN-DEPENDENT PROTEIN-KINASE

被引:110
作者
MCKEE, AC
KOSIK, KS
KENNEDY, MB
KOWALL, NW
机构
[1] MASSACHUSETTS GEN HOSP,DEPT NEUROL,BOSTON,MA 02114
[2] CALTECH,DIV BIOL,PASADENA,CA 91125
[3] HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,CTR NEUROL DIS,BOSTON,MA 02115
关键词
Alzheimer’s disease; Calcium/calmodulin-dependent kinase II; Hippocampus; Protein kinase; Tau protein;
D O I
10.1097/00005072-199001000-00006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The microtubule-associated phosphoprotein, tau, is an integral component of paired helical filaments in Alzheimer neurofibrillary tangles (NFT). The mechanism of NFT formation is unknown but aberrant phosphorylation of tau may be contributory. Calcium/calmodulin-dependent protein kinase type II (CaM kinase II), the most abundant kinase in the brain, phosphorylates tau in vitro. We found CaM kinase II immunoreactivity concentrated in human hippocampal pyramidal neurons of CA1 and the subiculum. In Alzheimer’s disease (AD) staining intensity of CA1 and subicular neurons is strikingly increased despite NFT formation and neuronal depletion. Enhanced CaM kinase II activity, possibly a result of deafferentation, may contribute to phosphorylation of tau protein leading to NFT deposition and neuronal death in AD © 1990 by the American Association of Neuropathologists.
引用
收藏
页码:49 / 63
页数:15
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