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首页> 外文期刊>Journal of Molecular and Cellular Cardiology >Sub-microscopic analysis of t-tubule geometry in living cardiac ventricular myocytes using a shape-based analysis method
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Sub-microscopic analysis of t-tubule geometry in living cardiac ventricular myocytes using a shape-based analysis method

机译:使用基于形状的分析方法的生物心室肌细胞中T型小管几何形状的亚微观分析

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摘要

Abstract Transverse-axial tubules (TTs) are key structures involved in cardiac excitation-contraction coupling and can become deranged in disease. Although optical measurement of TTs is frequently employed to assess TT abundance and regularity, TT dimensions are generally below the diffraction limit of optical microscopy so determination of tubule size is problematic. TT diameter was measured by labeling both local surface membrane area and volume with fluorescent probes (FM4-64 and calcein, respectively), correcting image asymmetry by image processing and using the relationship between surface area and volume for a geometric primitive. This method shows that TTs have a mean (± SEM) diameter of 356 ± 18 nm in rabbit and 169 ± 15 nm in mouse ( p 0.001). Rabbit TT diameters were more variable than those of mouse ( p 0.01) and the smallest TT detected was 41 nm in mouse and the largest 695 nm in rabbit. These estimates are consistent with TT diameters derived from the more limited sampling of high-pressure frozen samples by electron tomography (which examines only a small fraction of the cell volume). Other measures of TT abundance and geometry (such as volume, membrane fractions and direction) were also derived. On the physiological time scale of E-C coupling (milliseconds), the average TT electrical space constant is ~ 175 μm in rabbit and ~ 120 μm in mouse and is ~ 50% of the steady-state space constant. This is sufficient to ensure reasonable electrical uniformity across normal cells. The image processing strategy and shape-based 3D approach to feature quantification is also generally applicable to other problems in quantification of sub-cellular anatomy. Highlights ? Living cardiomyocytes were dual-labeled with fluorescent surface and volume probes. ? A novel 3D image processing strategy enabled calculation of t-tubule diameter. ? The method shows rabbit and mouse t-tubules have quite different morphologies. ? Mean diameters of rabbit and mouse t-tubules were 360 and 170 nm, respectively. ? Estimated electrical space constants are sufficient to ensure electrical uniformity. ]]>
机译:摘要横向轴管(TTS)是涉及心脏激发收缩偶联的关键结构,并且可以在疾病中变得紊乱。尽管TTS的光学测量经常用于评估TT丰度和规律性,但TT尺寸通常低于光学显微镜的衍射极限,因此小管尺寸的测定是有问题的。通过用荧光探针(分别用荧光探针(分别为CLCEIN)标记局部表面膜面积和体积,通过图像处理来校正图像不对称,并使用表面积与几何原始的体积之间的关系来测量TT直径。该方法表明,TTS在兔中具有356±18nm的平均直径(±18nm,小鼠169±15nm(P <0.001)。兔TT直径比小鼠(P <0.01)的变量更具变量,并且检测到的最小TT在小鼠中为41nm,兔中最大的695nm。这些估计与通过电子断层扫描(仅检查细胞体积的小部分)的高压冷冻样品的高压冻结样品的更有限采样而符合TT直径。还导出了其他TT丰度和几何测量措施(如体积,膜级分和方向)。在E-C耦合(毫秒)的生理时间尺度上,平均TT电空间常数在兔中〜175μm,小鼠〜120μm,是稳态空间常数〜50%。这足以确保跨越正常细胞的合理电均匀性。特征量化的图像处理策略和基于形状的3D方法通常适用于亚蜂窝解剖学的量化中的其他问题。强调 ?生物心肌细胞用荧光表面和体积探针双标记。还一种新颖的3D图像处理策略,使得计算T型管直径。还该方法显示兔和小鼠T-小管具有相当不同的形态。还兔子和小鼠T小管的平均直径分别为360和170nm。还估计的电气空间常数足以确保电均匀性。 ]]>

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