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Scanning ion conductance microscopy: a convergent high-resolution technology for multi-parametric analysis of living cardiovascular cells

机译:扫描离子电导显微镜:用于活体心血管细胞多参数分析的融合高分辨率技术

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摘要

Cardiovascular diseases are complex pathologies that include alterations of various cell functions at the levels of intact tissue, single cells and subcellular signalling compartments. Conventional techniques to study these processes are extremely divergent and rely on a combination of individual methods, which usually provide spatially and temporally limited information on single parameters of interest. This review describes scanning ion conductance microscopy (SICM) as a novel versatile technique capable of simultaneously reporting various structural and functional parameters at nanometre resolution in living cardiovascular cells at the level of the whole tissue, single cells and at the subcellular level, to investigate the mechanisms of cardiovascular disease. SICM is a multimodal imaging technology that allows concurrent and dynamic analysis of membrane morphology and various functional parameters (cell volume, membrane potentials, cellular contraction, single ion-channel currents and some parameters of intracellular signalling) in intact living cardiovascular cells and tissues with nanometre resolution at different levels of organization (tissue, cellular and subcellular levels). Using this technique, we showed that at the tissue level, cell orientation in the inner and outer aortic arch distinguishes atheroprone and atheroprotected regions. At the cellular level, heart failure leads to a pronounced loss of T-tubules in cardiac myocytes accompanied by a reduction in Z-groove ratio. We also demonstrated the capability of SICM to measure the entire cell volume as an index of cellular hypertrophy. This method can be further combined with fluorescence to simultaneously measure cardiomyocyte contraction and intracellular calcium transients or to map subcellular localization of membrane receptors coupled to cyclic adenosine monophosphate production. The SICM pipette can be used for patch-clamp recordings of membrane potential and single channel currents. In conclusion, SICM provides a highly informative multimodal imaging platform for functional analysis of the mechanisms of cardiovascular diseases, which should facilitate identification of novel therapeutic strategies.
机译:心血管疾病是复杂的病理,包括在完整组织,单细胞和亚细胞信号传导区隔水平上各种细胞功能的改变。用于研究这些过程的常规技术极为不同,并且依赖于各种方法的组合,这些方法通常会提供有关单个目标参数的时空有限的信息。这篇综述将扫描离子电导显微镜(SICM)描述为一种新颖的通用技术,它能够同时报告整个组织,单个细胞和亚细胞水平上活的心血管细胞中纳米分辨率下的各种结构和功能参数,从而研究心血管疾病的机制。 SICM是一种多峰成像技术,可以在完整的纳米活体心血管细胞和组织中同时动态分析膜形态和各种功能参数(细胞体积,膜电位,细胞收缩,单离子通道电流和细胞内信号传导的某些参数)在不同组织水平(组织,细胞和亚细胞水平)的分辨率。使用这项技术,我们表明,在组织水平上,内外主动脉弓内的细胞方向可以区分动脉粥样硬化和动脉粥样硬化保护区域。在细胞水平上,心力衰竭导致心肌细胞中T管的明显丧失,同时Z沟比率降低。我们还证明了SICM能够测量整个细胞体积作为细胞肥大的指标。此方法可以进一步与荧光结合使用,以同时测量心肌细胞收缩和细胞内钙瞬变,或绘制与环状单磷酸腺苷偶联的膜受体的亚细胞定位。 SICM移液器可用于膜电位和单通道电流的膜片钳记录。总之,SICM为心血管疾病机制的功能分析提供了高度有用的多模式成像平台,这应有助于确定新的治疗策略。

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