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IP3R1基因敲除小鼠培养的小脑细胞中钙动力学的改变

Altered calcium dynamics in cultured cerebellar cells from IP3R1-deficient mice.

作者信息

Matsumoto M, Kato K

机构信息

Developmental Neurobiology Laboratory, Brain Science Institute, Institute of Physical and Chemical Research (RIKEN) Hirosawa 2-1, Wako-shi, Saitama 351-0106, Japan.

出版信息

Neuroreport. 2001 Nov 16;12(16):3471-4. doi: 10.1097/00001756-200111160-00019.

Abstract

Intracellular calcium release in response to bath-applied quisqualate or caffeine was examined in cerebellar primary cultures of type-1-inositol-1,4,5-trisphosphate-receptor (IP3R1)- deficient mice. Under [Ca2+]o-free conditions, calcium release in response to 10 microM quisqualate was significantly reduced in Purkinje cells, but was unaffected in granule cells, suggesting that different subtypes of IP3 receptors contribute to the metabotropic glutamate response in these cells. In addition, calcium release in response to 10 mM caffeine under [Ca2+]o-free conditions was not impaired in cerebellar cells, suggesting that IICR and CICR are independently regulated in cerebellar cells. Moreover, in both wild-type and homozygous mutant mice, CICR in granule cells was approximately 6 times greater than in Purkinje cells.

摘要

在1型肌醇-1,4,5-三磷酸受体(IP3R1)缺陷小鼠的小脑原代培养物中,检测了对浴应用喹啉酸或咖啡因的细胞内钙释放情况。在无细胞外钙离子([Ca2+]o)的条件下,浦肯野细胞对10微摩尔喹啉酸的钙释放显著减少,但颗粒细胞不受影响,这表明不同亚型的IP3受体参与了这些细胞中的代谢型谷氨酸反应。此外,在无[Ca2+]o条件下,小脑细胞对10毫摩尔咖啡因的钙释放未受损,这表明在小脑细胞中,肌醇1,4,5-三磷酸受体介导的钙释放(IICR)和咖啡因诱导的钙释放(CICR)是独立调节的。此外,在野生型和纯合突变小鼠中,颗粒细胞中的CICR均比浦肯野细胞中的大约大6倍。

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