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Mattheyses, A.

Publications and source records attributed to Mattheyses, A..

2 recordsLinked to original sources

Fluid shear stress has a biphasic effect on clathrin-mediated endocytosis in vascular endothelial cells

Vascular endothelial cells (ECs) form a monolayer lining blood vessels and serve as a barrier between blood and tissues. Clathrin-mediated endocytosis (CME) is a major internalization pathway that involves a physical conformational change of the plasma membrane to form a vesicle and is therefore sensitive to the local environment. ECs are subjected to a myriad of fluid shear stress (FSS) rates from circulating blood, which we hypothesize affects CME. To test this, we used simultaneous two-wavelength axial ratiometry (STAR) microscopy, which provides nanoscale axial resolution, to determine the frequency and morphology of clathrin-coated vesicles as they form. Human umbilical vein endothelial cells (HUVECs) were transfected with dual-tagged clathrin light chain a (CLCa-iRFP-EGFP) and cultured under 10 dyn/cm2 FSS. CME activity was elevated in cells cultured under flow and assayed in static or flow conditions compared to statically cultured and imaged controls, indicating that FSS-induced changes to CME were maintained shortly after flow cessation. Single vesicle analysis showed cells cultured in FSS had a slight preference for vesicle formation with a flat-to-curved clathrin transition compared to control. Next, to assess the impact of different FSS rates, we cultured HUVECs at 20 and 40 dyn/cm2 FSS. We found total CME frequency was elevated compared to control at 20 dyn/cm2, but not 40 dyn/cm2. HUVECs cultured at both 20 and 40 dyn/cm2 had vesicles with increased lifetime and enhanced stability, as well as a higher proportion of vesicles formed through a flat-to-curved transition of clathrin.

Cell Biology↗

OOPS: Object-Oriented Polarization Software for analysis of fluorescence polarization microscopy images

Most essential cellular functions are performed by proteins assembled into larger complexes. Fluorescence Polarization Microscopy (FPM) is a powerful technique that goes beyond traditional imaging methods by allowing researchers to measure not only the localization of proteins within cells, but also their orientation or alignment within complexes or cellular structures. FPM can be easily integrated into standard widefield microscopes with the addition of a polarization modulator. However, the extensive image processing and analysis required to interpret the data have limited its widespread adoption. To overcome these challenges and enhance accessibility, we introduce OOPS (Object-Oriented Polarization Software), a MATLAB-based analysis tool tailored for FPM data. This work highlights the distinctive features of our software, which empower researchers to efficiently manage large datasets; detect and analyze individual structures; conduct population assessments based on morphology, intensity, and polarization-specific parameters; and create publication-quality visualizations, all within a user-friendly graphical interface. Importantly, OOPS is adaptable to various sample types, labeling techniques, and imaging setups, facilitating in-depth analysis of diverse polarization-sensitive samples. Here, we demonstrate the power and versatility of our approach by applying OOPS to FPM images of both punctate and filamentous structures. OOPS is freely available under the GNU GPL 3.0 license and can be downloaded at https://github.com/Mattheyses-Lab/OOPS.

cell biology↗