研究荚膜细胞肌动蛋白形态的红色荧光生命活动标记物

Eva Wiesner, Julia Binz-Lotter, Simon E. Troeder, David Unnersjoe-Jess, Nelli Rutkowski, Branko Zevnik, Thomas Benzing, Roland Wedlich-Soldner, Matthias J. Hackl
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摘要

肌动蛋白是细胞细胞骨架的主要组成部分,负责维持细胞形状、促进运动和细胞内运输。在肾脏中,肾小球荚膜细胞高度依赖肌动蛋白细胞骨架塑造其独特的足部过程。肌动蛋白结合蛋白的遗传突变会导致局灶节段性肾小球硬化,而其他器官则基本不受影响。迄今为止,荚膜细胞中肌动蛋白的可视化仅限于电子显微镜或肌动蛋白结合蛋白的间接免疫荧光标记。然而,短的 F-肌动蛋白结合肽 Lifeact 使研究人员能够在体外和体内研究肌动蛋白的动态,而对肌动蛋白代谢的干扰最小。Cre 重组酶介导的活性允许在荚膜细胞中进行细胞特异性和镶嵌表达,使单个细胞的选择性标记与邻近的非表达细胞形成对比。转基因小鼠出生时非常健康,幼鼠也没有表现出与肾脏有关的表型。通过眼内成像和超分辨率显微镜,我们以以前只能通过电子显微镜获得的分辨率显示了肌动蛋白在足突的亚细胞定位。我们的新型小鼠品系为通过体内成像和其他传统光镜技术研究荚膜细胞和其他细胞类型的肌动蛋白细胞骨架提供了机会。
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A Red Fluorescent Lifeact Marker to Study Actin Morphology in Podocytes
F-actin is a major component of the cellular cytoskeleton, responsible for maintaining cell shape, enabling movement and facilitating intracellular transport. In the kidney, glomerular podocytes are highly dependent on their actin cytoskeleton shaping their unique foot processes. Hereditary mutations in actin-binding proteins cause focal segmental glomerulosclerosis, while other organs remain largely unaffected. So far, actin visualization in podocytes has been limited to electron microscopy or indirect immunofluorescent labeling of actin-binding proteins. However, the short F-actin-binding peptide Lifeact enables researchers to study actin dynamics in vitro and in vivo with minimal interference with actin metabolism. Here we introduce a new mouse model with conditional expression of a Lifeact.mScarlet I fusion protein providing red labeling of actin. Cre recombinase-mediated activity allows cell-specific and mosaic expression in podocytes, enabling selective labeling of individual cells to contrast with non-expressing neighboring cells. Transgenic mice are born healthy and young animals display no kidney-related phenotype. By intravital imaging and super-resolution microscopy, we show subcellular localization of actin to the foot processes in a resolution previously only obtainable by electron microscopy. Our novel mouse line provides the opportunity to study the actin cytoskeleton in podocytes and other cell types by intravital imaging and other conventional light microscopy techniques.
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