Cornelius Faber

Purpose Time‐lapse MRI enables tracking of single iron‐labeled cells. Yet, due to temporal blurring, only slowly moving cells can be resolved. To study faster cells for example during inflammatory processes, accelerated acquisition is needed. Methods A rotating phantom system was developed to quantitatively measure the current maximum detectable speed of cells in time‐lapse MRI. For accelerated cell tracking, an interleaved radial acquisition scheme was applied to phantom and murine brain in vivo time‐lapse MRI experiments at 9.4 T. Detection of iron‐labeled cells was evaluated in fully sampled and undersampled reconstructions with and without compressed sensing. Results The rotating phantom system enabled ultra‐slow rotation of phantoms and a velocity detection limit of full‐brain Cartesian time‐lapse MRI of up to 172 μm/min was determined. Both phantom and in vivo measurements showed that single cells can be followed dynamically using radial time‐lapse MRI. Higher temporal resolution of undersampled reconstructions reduced geometric distortion, the velocity detection limit was increased to 1.1 mm/min in vitro, and previously hidden fast‐moving cells were recovered. In the mouse brain after in vivo labeling, a total of 42 ± 4 cells were counted in fully sampled, but only 7 ± 1 in undersampled images due to streaking artifacts. Using compressed sensing 33 ± 4 cells were detected. Conclusion Interleaved radial time‐lapse MRI permits retrospective reconstruction of both fully sampled and accelerated images, enables single cell tracking at higher temporal resolution and recovers cells hidden before due to blurring. The velocity detection limit as determined with the rotating phantom system increased two‐ to three‐fold compared to previous results.