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组胺可诱导原代培养的大鼠脑星形胶质细胞线粒体游离钙离子浓度产生振荡。

Histamine induces oscillations of mitochondrial free Ca2+ concentration in single cultured rat brain astrocytes.

作者信息

Jou M J, Peng T I, Sheu S S

机构信息

Department of Pharmacology and Physiology, School of Medicine and Dentistry, University of Rochester, NY 14642-8711, USA.

出版信息

J Physiol. 1996 Dec 1;497 ( Pt 2)(Pt 2):299-308. doi: 10.1113/jphysiol.1996.sp021769.

Abstract
  1. The free Ca2+ concentration of mitochondria ([Ca2+]m) in cultured rat brain astrocytes was measured with a fluorescent Ca2+ indicator, rhod-2, and laser confocal microscopy. 2. Confocal images revealed a rhod-2 distribution that matched mitochondrial localization. 3. Using a Ca2+ ionophore, ionomycin, to clamp the [Ca2+]m from 0 to 100 microM in order to obtain the minimal and maximal fluorescence of rhod-2 in situ, a 3.5 +/- 0.4-fold increase in fluorescence intensity was observed, suggesting that the fluorescence of intramitochondrial rhod-2 was responding in a Ca(2+)-sensitive manner, thereby allowing measurements of [Ca2+]m in single astrocytes. 4. Exposure of fura-2-loaded astrocytes to 100 microM histamine produced a rapid and transient increase in cytosolic Ca2+ concentration ([Ca2+]c) that lasted for several tens of seconds. The spike in [Ca2+]c was frequently followed by variable numbers of repetitive oscillations of Ca2+, which appeared to dampen in amplitude with time. 5. This pattern of histamine-induced [Ca2+]c oscillations was also observed in rhod-2-loaded cells suggesting that [Ca2+]m fluctuated with a similar frequency. 6. The oscillations of [Ca2+]m, but not of [Ca2+]c, were abolished by a proton ionophore, carbonyl cyanide m-chlorophenyl-hydrazone (CCCP), and by Ruthenium Red, a mitochondrial Ca(2+)-uniporter inhibitor. 7. These results suggest that the mitochondrial Ca2+ transport systems in cultured rat brain astrocytes are able to relay receptor-mediated [Ca2+]m oscillations into mitochondria.
摘要
  1. 用荧光钙指示剂罗丹明-2(rhod-2)和激光共聚焦显微镜测量培养的大鼠脑星形胶质细胞中线粒体的游离钙离子浓度([Ca2+]m)。2. 共聚焦图像显示罗丹明-2的分布与线粒体定位相符。3. 使用钙离子载体离子霉素将[Ca2+]m从0钳制到100微摩尔,以获得原位罗丹明-2的最小和最大荧光,观察到荧光强度增加了3.5±0.4倍,表明线粒体内罗丹明-2的荧光以钙敏感方式响应,从而能够测量单个星形胶质细胞中的[Ca2+]m。4. 用100微摩尔组胺处理负载fura-2的星形胶质细胞,导致胞质钙离子浓度([Ca2+]c)迅速短暂升高,持续数十秒。[Ca2+]c的峰值之后经常伴随着数量不等的钙离子重复振荡,其幅度似乎随时间衰减。5. 在负载罗丹明-2的细胞中也观察到这种组胺诱导的[Ca2+]c振荡模式,表明[Ca2+]m以相似频率波动。6. 质子离子载体羰基氰化物间氯苯腙(CCCP)和线粒体钙单向转运体抑制剂钌红消除了[Ca2+]m的振荡,但未消除[Ca2+]c的振荡。7. 这些结果表明,培养的大鼠脑星形胶质细胞中的线粒体钙转运系统能够将受体介导的[Ca2+]m振荡传递到线粒体中。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc3a/1160985/77fe9fc35b39/jphysiol00386-0007-a.jpg

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