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Cytoplasmic motions, rheology, and structure probed by a novel magnetic particle method

机译:新型磁性粒子方法探测的细胞质运动,流变学和结构

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摘要

The motions of magnetic particles contained within organelles of living cells were followed by measuring magnetic fields generated by the particles. The alignment of particles was sensed magnetometrically and was manipulated by external fields, allowing non-invasive detection of particle motion as well as examination of cytoplasmic viscoelasticity. Motility and rheology data are presented for pulmonary macrophages isolated from lungs of hamsters 1 d after the animals had breathed airborne gamma-Fe2O3 particles. The magnetic directions of particles within phagosomes and secondary lysosomes were aligned, and the weak magnetic field produced by the particles was recorded. For dead cells, this remanent field was constant, but for viable macrophages, the remanent field decreased rapidly so that only 42% of its initial magnitude remained 5 min after alignment. A twisting field was applied perpendicular to the direction of alignment and the rate at which particles reoriented to this new direction was followed. The same twisting was repeated for particles suspended in a series of viscosity standards. Based on this approach, the low-shear apparent intracellular viscosity was estimated to be 1.2-2.7 X 10(3) Pa.s (1.2-2.7 X 10(4) poise). Time-lapse video microscopy confirmed the alignment of ingested particles upon magnetization and showed persistent cellular motility during randomization of alignment. Cytochalasin D and low temperature both reduced cytoplasmic activity and remanent-field decay, but affected rheology differently. Magnetic particles were observed in association with the microtubule organizing center by immunofluorescence microscopy; magnetization did not affect microtubule distribution. However, both vimentin intermediate filaments and f-actin reorganized after magnetization. These data demonstrate that magnetometry of isolated phagocytic cells can probe organelle movements, rheology, and physical properties of the cytoskeleton in living cells.
机译:包含在活细胞细胞器中的磁性粒子的运动是通过测量粒子产生的磁场来进行的。颗粒的排列通过磁力法进行检测,并通过外部磁场进行操作,从而可以无创地检测颗粒运动以及检查细胞质的粘弹性。提供了动物呼吸空气中的γ-Fe2O3颗粒后1天从仓鼠肺中分离出的肺巨噬细胞的运动和流变学数据。吞噬体和次级溶酶体内的颗粒磁方向对齐,并记录由颗粒产生的弱磁场。对于死细胞,该残留磁场是恒定的,但是对于有活力的巨噬细胞,残留磁场迅速减小,因此在对齐后5分钟仅保留其初始大小的42%。垂直于取向方向施加扭曲场,并遵循粒子重新定向到该新方向的速率。对于悬浮在一系列粘度标准中的颗粒,重复相同的扭曲操作。基于这种方法,低剪切表观细胞内粘度估计为1.2-2.7 X 10(3)Pa.s(1.2-2.7 X 10(4)泊)。延时视频显微镜证实了磁化后摄入颗粒的排列,并在排列随机化过程中显示出持续的细胞运动性。细胞松弛素D和低温都降低了细胞质活性和剩余磁场衰减,但对流变学的影响不同。通过免疫荧光显微镜观察到与微管组织中心相关的磁性颗粒。磁化强度不影响微管分布。但是,波形蛋白中间丝和f-肌动蛋白在磁化后都发生了重组。这些数据表明,分离的吞噬细胞的磁力测定法可以探测活细胞中细胞器的运动,流变性和细胞骨架的物理特性。

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