Objective: We propose a novel flexible and entirely stretchable radiofrequency coil for magnetic resonance imaging. This coil design aims at increasing patient comfort during imaging while maintaining or improving image quality. Methods: Conductive silver-coated thread was zigzag stitched onto stretchable athletic fabric to create a single-loop receive coil. The stitched coil was mounted in draped and stretched fashions and compared to a coil fabricated on flexible printed circuit board. Match/tune circuits, detuning circuits, and baluns were incorporated into the final setup for bench measurements and imaging on a 3T MR scanner. A fast spin echo sequence was used to obtain images for comparison. Results: The fabricated coil presents multi-directional stretchability and flexibility while maintaining conductivity and stitch integrity. SNR calculations show that this stretchable coil design is comparable to a flexible, standard PCB coil with a 13-30% decrease in SNR depending on stretch degree and direction. In vivo human wrist images were obtained using the stitched coil. Conclusion: Despite the reduction in SNR for this combination of materials, there is a reduced percentage of SNR drop as compared to existing stretch coil designs. These imaging results and calculations support further experimentation into more complex coil geometries. Significance: This coil is uniquely stretchable in all directions, allowing for joint imaging at various degrees of flexion, while offering the closest proximity of placement to the skin. The materials provide a similar level of comfort to athletic wear and could be incorporated into coils for a variety of anatomies.
Osteocytes are the most abundant cells in bone, which is a frequent site of breast cancer metastasis. Here, we focused on Wnt signaling and evaluated tumor-osteocyte interactions. In animal experiments, mammary tumor cells were inoculated into the mammary fat pad and tibia. The role of Lrp5-mediated Wnt signaling was examined by overexpressing and silencing Lrp5 in osteocytes and establishing a conditional knockout mouse model. The results revealed that administration of osteocytes or their conditioned medium (CM) inhibited tumor progression and osteolysis. Osteocytes overexpressing Lrp5 or β-catenin displayed strikingly elevated tumor-suppressive activity, accompanied by downregulation of tumor-promoting chemokines and upregulation of apoptosis-inducing and tumor-suppressing proteins such as p53. The antitumor effect was also observed with osteocyte-derived CM that was pretreated with a Wnt-activating compound. Notably, silencing Lrp5 in tumors inhibited tumor progression, while silencing Lrp5 in osteocytes in conditional knockout mice promoted tumor progression. Osteocytes exhibited elevated Lrp5 expression in response to tumor cells, implying that osteocytes protect bone through canonical Wnt signaling. Thus, our results suggest that the Lrp5/β-catenin axis activates tumor-promoting signaling in tumor cells but tumor-suppressive signaling in osteocytes. We envision that osteocytes with Wnt activation potentially offer a novel cell-based therapy for breast cancer and osteolytic bone metastasis.
To enable high spatial and temporal breast imaging resolution via combined use of high field MRI, array coils, and forced current excitation (FCE) multi channel transmit. A unilateral 16-channel receive array insert was designed for use in a transmit volume coil optimized for quadrature operation with dual-transmit RF shimming at 7T. Signal-to-noise ratio (SNR) maps, g-factor maps, and high spatial and temporal resolution in vivo images were acquired to demonstrate the utility of the coil architecture. The dual-transmit FCE coil provided homogeneous excitation and the array provided an increase in average SNR of 3.3 times (max 10.8, min 1.5) compared to the volume coil in transmit/receive mode. High resolution accelerated in vivo breast imaging demonstrated the ability to achieve isotropic spatial resolution of 0.5 mm within clinically relevant 90 s scan times, as well as the ability to perform 1.0 mm isotropic resolution imaging, 7 s per dynamics, with the use of bidirectional SENSE acceleration of up to R = 9. The FCE design of the transmit coil easily accommodates the addition of a sixteen channel array coil. The improved spatial and temporal resolution provided by the high-field array coil with FCE dual-channel transmit will ultimately be beneficial in lesion detection and characterization.