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Binz-Lotter, J.

Publications and source records attributed to Binz-Lotter, J..

2 recordsLinked to original sources

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.

cell biology↗

Correlation of calcium multiphoton with ultrastructural STED imaging of the slit diaphragm in the same glomerulus.

In recent years functional multiphoton imaging of viable mouse tissue and STED imaging of optically cleared tissues allowed new insights into kidney biology. Here, we present a novel workflow where multiphoton imaging of calcium signals in podocytes is, in the same glomerulus, correlated with super-resolved STED imaging and analysis of the slit diaphragm (SD) morphology. Mice expressing the calcium indicator GCaMP3 exclusively in podocytes served as healthy controls and were challenged with two different doses of nephrotoxic serum (NTS). NTS-induced SD architecture damage increased in a dose-dependent manner, whereas intracellular calcium levels exhibited a wide range of variation and showed no correlation with SD damage in the same glomerulus. Our co-imaging protocol is applicable to a broad range of research questions as it is suitable for other tissues and compatible with a variety of reporters and tissue antigens. Translational statementThe combination of multiphoton and super-resolution microscopy identifies the modulation of signaling pathways and resolves the changes in ultrastructure in disease states in the same glomeruli. Using our new method, we can compare functional and morphological data to investigate the degree of correlation to reveal novel underlying pathomechanism. This knowledge can improve our ability to draw conclusions from human kidney biopsies, in which the ultrastructure will be assessed more-often by routine super-resolution microscopy in the future.

cell biology↗