High-Resolution Imaging of Intracellular Calcium Fluctuations Caused by Oscillating Microbubbles
Inés Beekers (Erasmus MC)
Frits Mastik (Erasmus MC)
Robert Beurskens (Erasmus MC)
Phoei Ying Tang (Erasmus MC)
Merel Vegter (Erasmus MC)
Antonius F.W. van der Steen (Erasmus MC, TU Delft - ImPhys/Medical Imaging)
N. de Jong (Erasmus MC, TU Delft - ImPhys/Medical Imaging)
M.D. Verweij (TU Delft - ImPhys/Medical Imaging, Erasmus MC)
Klazina Kooiman (Erasmus MC)
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Abstract
Ultrasound insonification of microbubbles can locally enhance drug delivery, but the microbubble–cell interaction remains poorly understood. Because intracellular calcium (Cai 2+) is a key cellular regulator, unraveling the Cai 2+ fluctuations caused by an oscillating microbubble provides crucial insight into the underlying bio-effects. Therefore, we developed an optical imaging system at nanometer and nanosecond resolution that can resolve Cai 2+ fluctuations and microbubble oscillations. Using this system, we clearly distinguished three Cai 2+ uptake profiles upon sonoporation of endothelial cells, which strongly correlated with the microbubble oscillation amplitude, severity of sonoporation and opening of cell–cell contacts. We found a narrow operating range for viable drug delivery without lethal cell damage. Moreover, adjacent cells were affected by a calcium wave propagating at 15 μm/s. With the unique optical system, we unraveled the microbubble oscillation behavior required for drug delivery and Cai 2+ fluctuations, providing new insight into the microbubble–cell interaction to aid clinical translation.