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Updated: May 27, 2026

Two-photon Imaging of Intracellular Ca2+ Handling and Nitric Oxide Production in Endothelial and Smooth Muscle Cells of an Isolated Rat Aorta
Published on: June 10, 2015
Imaging of vascular smooth muscle cells with soft X-ray spectromicroscopy
Julia Sedlmair1, Sophie-Charlotte Gleber, Semra Öztürk Mert
1Institute for X-Ray Physics, Georg-August-University Göttingen, Friedrich-Hund-Pl. 1, D-37077 Göttingen, Germany. jsedlma@gwdg.de
Abstract:
Using X-ray microscopy and spectromicroscopy, vascular smooth muscle cells (VSMCs) were imaged, prepared without using additional embedding material or staining, but by applying simple, noncryo fixation techniques. The cells were imaged with a compact source transmission X-ray microscope and a scanning transmission X-ray microscope (STXM). With the STXM, spectromicroscopy was performed at the C K-edge and the Ca L(III,II)-edges. VSMCs were chosen because of their high amount of actin stress fibers, so that the actin cytoskeleton should be visible. Other parts of the cell, such as the nucleus and organelles, were also identified from the micrographs. Both in the spectra and the images, the effects of the different preparation procedures were observable. Furthermore, Ca hotspots were detected and their density is determined.
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