Presentation
13 March 2024 Combined optical coherence microscopy and confocal microscopy of a 3D, co-culture model of aortic valve calcification
Author Affiliations +
Abstract
Longitudinal imaging of a 3D model of calcific aortic valve disease, which consisted of co-cultured GFP+ Valve Endothelial Cells (VEC) and Valve Interstitial Cells (VIC), was performed with a combined Optical Coherence Microscopy (OCM), confocal reflectance and fluorescence microscopy system. The acquired confocal volumes depicted the VEC morphological changes and migration as well as collagen fiber alignment. With the aid of computational refocusing and multi-volume processing, the OCM datasets could visualize VIC cell bodies, matrix remodeling, nodule formation and calcific deposits. The complementary information derived using this combined approach could help unravel the cellular mechanisms leading to aortic valve calcification.
Conference Presentation
© (2024) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Santosh Balakrishnan, Meg McFetridge, Katherine M. Driscoll, Yuechuan Lin, Nichaluk Leartprapun, Jonathan T. Butcher, and Steven G. Adie "Combined optical coherence microscopy and confocal microscopy of a 3D, co-culture model of aortic valve calcification", Proc. SPIE 12819, Diagnostic and Therapeutic Applications of Light in Cardiology 2024, 128190T (13 March 2024); https://doi.org/10.1117/12.3001787
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KEYWORDS
3D modeling

Confocal microscopy

Optical coherence microscopy

Diseases and disorders

Collagen

Visualization

Image processing

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