Department of Neuroscience, Mt. Sinai School of Medicine, One Gustave Levy Place, New York, New York, USA.
ACS Chem Neurosci. 2010 Aug 18;1(8):575-85. doi: 10.1021/cn100052v. Epub 2010 Jun 15.
We have developed a caged IP(3) analogue for two-photon photolysis in living animals. This probe is a cell permeable version and was coloaded with a fluorescent Ca(2+) dye into astrocytes in layer 1 of the somatosensory cortex of anesthetized mice. Two-photon irradiation of single cells at 720 nm produced rapid and robust increases in intracellular Ca(2+) concentrations monitored using two-photon microscopy at 950 nm. The photoevoked intracellular Ca(2+) waves were similar in magnitude to intrinsic signals in wild type mice. These waves did not propagate to other cells beyond the targeted astrocyte. In contrast, we observed intercellular astrocytic Ca(2+) waves in two mouse models of familial Alzheimer's disease. These data suggest that Alzheimer's might perturb gliotransmission but not IP(3) signaling per se in mouse models of the disease.
我们开发了一种笼状 IP(3)类似物,用于活体内动物的双光子光解。这种探针是一种细胞通透型,与荧光 Ca(2+)染料共载入麻醉小鼠体感皮层 1 层的星形胶质细胞中。在 720nm 处对单个细胞进行双光子辐照,使用 950nm 处的双光子显微镜监测,可快速产生并增强细胞内 Ca(2+)浓度。光诱发的细胞内 Ca(2+)波的幅度与野生型小鼠的固有信号相似。这些波不会在靶星形胶质细胞之外的其他细胞中传播。相比之下,我们在两种家族性阿尔茨海默病的小鼠模型中观察到细胞间星形胶质细胞 Ca(2+)波。这些数据表明,阿尔茨海默病可能会扰乱神经胶质传递,但不会扰乱疾病小鼠模型中 IP(3)信号本身。