首页> 外文期刊>Journal of Microscopy >COMPARISON OF TWO-PHOTON EXCITATION LASER SCANNING MICROSCOPY WITH UV-CONFOCAL LASER SCANNING MICROSCOPY IN THREE-DIMENSIONAL CALCIUM IMAGING USING THE FLUORESCENCE INDICATOR INDO-1
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COMPARISON OF TWO-PHOTON EXCITATION LASER SCANNING MICROSCOPY WITH UV-CONFOCAL LASER SCANNING MICROSCOPY IN THREE-DIMENSIONAL CALCIUM IMAGING USING THE FLUORESCENCE INDICATOR INDO-1

机译:荧光指示剂INDO-1对二维钙成像中两光子激发激光扫描显微镜与紫外共聚焦激光扫描显微镜的比较

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Two-photon excitation laser scanning fluorescence microscopy (2p-LSM) was compared with UV-excitation confocal laser scanning fluorescence microscopy (UV-CLSM) in terms of three-dimensional (3-D) calcium imaging of living cells in culture, Indo-1 was used as a calcium indicator. Since the excitation volume is more wavelengths are longer in 2p-LSM than 2p-LSM exhibited several advantages over UV-CLSM: (1) a lower level of background signal by a factor of 6-17, which enhances the contrast by a factor of 6-21; (2) a lower rate of photobleaching by a factor of 2-4; (3) slightly lower phototoxicity. When 3-D images were repeatedly acquired, the calcium concentration determined by UV-CLSM depended strongly on the number of data acquisitions and the nuclear regions falsely exhibited low calcium concentrations, probably due to an interplay of different levels of photobleaching of Indo-1 and autofluorescence, while the calcium concentration evaluated by 2p-LSM was stable and homogeneous throughout the cytoplasm, The spatial resolution of 2p-LSM was worse by 10% in the focal plane and by 30% along the optical axis due to the longer excitation wavelength, This disadvantage can be overcome by the addition of a confocal pinhole (two-photon excitation confocal laser scanning fluorescence microscopy), which made the resolution similar to that in UV-CLSM. These results indicate that 2p-LSM is preferable for repeated 3-D reconstruction of calcium concentration in living cells. In UV-CLSM, 0.18-mW laser power with a 2.6-phi pinhole (in normalized optical coordinate) gives better signal-to-noise ratio, contrast and resolution than 0.09-mW laser power with a 49-phi pinhole. However, since the damage to cells and the rate of photobleaching is substantially greater under the former condition, it is not suitable for repeated acquisition of 3-D images. [References: 14]
机译:在培养物中活细胞的三维(3-D)钙成像方面,将两光子激发激光扫描荧光显微镜(2p-LSM)与紫外线激发共聚焦激光扫描荧光显微镜(UV-CLSM)进行了比较1用作钙指示剂。由于2p-LSM的激发体积更多,因此波长比2p-LSM更长,与UV-CLSM相比显示出以下几个优点:(1)将背景信号的水平降低6-17倍,将对比度提高6倍6-21; (2)光漂白率降低2-4倍; (3)光毒性稍低。重复获取3-D图像时,由UV-CLSM确定的钙浓度在很大程度上取决于数据采集的数量,并且核区域错误地显示出低的钙浓度,这可能是由于Indo-1和Indo-1的不同水平的光漂白相互作用所致。自发荧光,虽然2p-LSM评估的钙浓度在整个细胞质中是稳定且均一的,但2p-LSM的空间分辨率在焦平面中差了10%,而在光轴上的空间分辨率差了,因为激发波长更长,可以通过添加共聚焦针孔(双光子激发共聚焦激光扫描荧光显微镜)来克服此缺点,该方法的分辨率类似于UV-CLSM。这些结果表明2p-LSM对于重复3-D重建活细胞中钙浓度是优选的。在UV-CLSM中,具有2.6phi针孔的0.18 mW激光功率(在归一化光学坐标下)比具有49 phi针孔的0.09 mW激光功率具有更好的信噪比,对比度和分辨率。但是,由于在前一种条件下对细胞的损害和光致漂白的速率明显更大,因此不适合重复采集3D图像。 [参考:14]

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