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Type 1 inositol 1,4,5-trisphosphate receptor knock-out mice: their phenotypes and their meaning in neuroscience and clinical practice
被引:40
作者:
Matsumoto, M
Nagata, E
机构:
[1] Univ Tokyo, Inst Phys & Chem Res, Brain Sci Inst, Minato Ku, Tokyo, Japan
[2] Univ Tokyo, Inst Med Sci, Dept Mol Neurobiol, Minato Ku, Tokyo, Japan
[3] Keio Univ, Dept Neurol, Tokyo, Japan
来源:
JOURNAL OF MOLECULAR MEDICINE-JMM
|
1999年
/
77卷
/
05期
关键词:
inositol 1,4,5-trisphosphate receptor;
calcium release from intracellular stores;
gene targeting;
ataxia;
epileptic seizures;
D O I:
10.1007/s001090050370
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Cytoplasmic calcium, which acts as a second messenger, is derived not only from outside the cell but also from intracellular stores. A receptor for inositol 1,4,5-trisphosphate (IP3), an intracellular second messenger, is located on these internal calcium stores and functions as a calcium releasing channel. The "type 1" IP3 receptor (IP(3)R1) is concentrated predominantly in cerebellar Purkinje cells and is also widely present in other neural and peripheral tissues, but many of its physiological roles in these cells are still unclear. We have previously succeeded in obtaining mice with disruption of this IP(3)R1 gene, in which brain IP3-induced calcium release was almost completely abolished. They were rarely born alive, indicating that IP(3)R1 has some functions during embryonic development. Animals exhibited severe neurological symptoms, ataxia and epilepsy, and were shown to be deficient in the cerebellar long-term depression. They give us promising clues regarding the physiological roles of calcium release from internal stores and serve as a model for the relevant human disease states.
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页码:406 / 411
页数:6
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