Pathogenic mechanism of calcium channelopathy
| Project/Area Number |
15300121
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Neurochemistry/Neuropharmacology
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| Research Institution | Tokyo Medical and Dental University |
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Principal Investigator |
TANABE Tsutomu Tokyo Medical and Dental University, Graduate School of Medicine, Professor, 大学院・医歯学総合研究科, 教授 (70183069)
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| Project Period (FY) |
2003 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥16,300,000 (Direct Cost: ¥16,300,000)
Fiscal Year 2005: ¥4,800,000 (Direct Cost: ¥4,800,000)
Fiscal Year 2004: ¥5,600,000 (Direct Cost: ¥5,600,000)
Fiscal Year 2003: ¥5,900,000 (Direct Cost: ¥5,900,000)
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| Keywords | Spinocerebellar ataxia type 6 / P-type calcium channel / Purkinje cell / Ca current / polyglutamine disease / SCA6 / Cav2 channel / knock-in mouse / FHM / EA2 |
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| Research Abstract |
Spinocerebellar ataxia type 6 (SCA6) is caused by polyglutamine expansion in P-type Ca channel and is characterized by predominant degeneration of cerebellar Purkinje cell. Although clinical and pathological features of each polyglutamine disease diverse widely, a common mechanism is presumed to underlie the pathogenesis inducing cytotoxicity. Polyglutamine expansion in SCA6 is within the normal range in other disease. Thus a different idea that functional alteration of the P-type Ca channel is causally related to pathophysiology of SCA6 has been emerged. Consistent with this idea several reports have been published showing SCA6 mutation induces alteration of channel properties. But these studies have been done using the non-neuronal cells. To characterize SCA6 mutation of P-type Ca channel in neuron especially in Purkinje cells, we have generated knock-in mouse models that express human P-type Ca^<2+> channel with SCA6 mutation. Patch-clamp recordings of the Purkinje cells from homozygous normal or SCA6 knock-in mice showed no alteration of channel properties by the SCA6 mutation. Thus SCA6 has been considered as one of channelopathies rather than a polyglutamine disease, our present results favors the idea that SCA6 is rather a polyglutamine disease. Therefore it may be important to explore the mechanism underlying SCA6 from the point of view of polyglutamine disease.
In line with this consideration, we have tested whether SCA6 mutation affects the channel localization. When using the primary cultured hippocampal neurons, SCA6 mutation did not modify the channel localization. Then we are currently conducting this study using cerebellar Purkinje cells.
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Report
(4 results)
Research Products
(26 results)
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[Journal Article] Leukemia inhibitory factor activates cardiac L-type Ca^<2+> channels via phosphorylation of serine 1829 in the rabbit Ca_v1.2 subunit2004
Author(s)
Takahashi, E., Fukuda, K., Miyoshi, S., Murata, M., Kato, T., Ita, M., Tanabe, T., Ogawa.S.
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Journal Title
Circulation Research 94
Pages: 1242-1248
Related Report
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[Journal Article] Blocking the R-type (Ca_v2.3) Ca^<2+> channel enhanced morphine analgesia and reduced morphine tolerance2004
Author(s)
Yokoyama, K., Kurihara, T., Saegusa, H., Zong, S., Makita, K., Tanabe, T.
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Journal Title
Eur.J.Neurosci. 20
Pages: 3516-3519
Related Report
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[Publications] Takei, T., Saegusa, H., Zong, S., Murakoshi, T., Makita, K., Tanabe, T.: "Anesthetic Sensitivities to Propofol and Halothane in Mice Lacking the R-type (Ca_v2.3)Ca^<2+> Channel."Anesthesia and Analgesia. 97. 96-103 (2003)
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[Publications] Takei, T., Saegusa, H., Zong, S., Murakoshi, T., Makita, K., Tanabe, T.: "Increased sensitivity to halothane but decreased sensitivity to propofol in mice lacking the N-type Ca^<2+> channel."Neuroscience Letters. 350. 41-45 (2003)
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