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Biology subjects

Kuddannaya, S.

Publications and source records attributed to Kuddannaya, S..

4 recordsLinked to original sources

Fast Dynamic Whole-Body In Vivo Cytometry Using Magnetic Particle Imaging

Rapid quantification of the immediate organ accumulation of injected stem cells remains a major challenge. We performed in vivo cytometry (non-invasive cell counting) with magnetic particle imaging (MPI) to track magnetically labeled cells in real-time on a time scale of minutes with high sensitivity, zero background signal, and simple linear quantification. Human mesenchymal stem cells (hMSCs, [~]25 {micro}m in diameter) and human neural precursor cells (hNPCs, [~]10 {micro}m in diameter) were labeled with ferucarbotran or Synomag(R)-D70 as superparamagnetic iron oxide (SPIOs), and tracked with MPI in mice to map their whole-body cell biodistribution after intravenous (IV) or intra-arterial (IA) injection. The organ site of cell accumulation and retention were dependent on cell type, injection route, and frequency of administration, with the lung and liver acting as the major entrapment organs. In vivo MPI enabled quantitative tracking of the dynamic clearance and redistribution of labeled cells, showing major differences between larger hMSCs and smaller hNPCs. Co-registered MRI/CT and histological validation confirmed the anatomical localization of SPIO-labeled cells including the brain following IA injection. Integrating MPI cytometry with preclinical and translational studies may aid in further optimization of the route, dose, and frequency of stem cell administration. One Sentence SummaryFast whole-body in vivo cytometry using MPI is able to dynamically track and quantify therapeutic stem cell accumulation.

bioengineering↗

MPI-Guided Photothermal Therapy of Prostate Cancer using Stem Cell Delivery of Magnetotheranostic Nanoflowers

Intratumoral nanoparticle (NP) injection is a commonly used for local hyperthermia. A limitation of this delivery route is the limited NP dispersion and retainment within the tumor, with undesired leakage leading to off-target toxicity. By exploiting their inherent tumor tropism, we have used human mesenchymal stem cells (hMSCs) as delivery vehicles for magnetic theranostic gold-iron oxide nanoflowers (GIONF) to improve their overall intratumoral distribution and retention. GIONF-loaded hMSCs exhibited excellent heating properties for laser photothermal therapy and high tracer performance for visualization and quantification by magnetic particle imaging (MPI). In contrast to naked GIONF, GIONF-hMSCs remained within the prostate tumors one week post-injection, with MPI-guided PTT completely ablating tumors without recurrence.

bioengineering↗

Cold Quad-Modal Nanocomplex for Precise and Quantitative in Vivo Stem Cell Tracking

Current single imaging modalities typically lack the ability to simultaneously offer detailed anatomical visualization and quantitative cellular information, which is crucial for evaluating and improving therapeutic efficacy. We developed a quad-modal imaging nanocomplex for magnetic resonance imaging (MRI), magnetic particle imaging (MPI), computed tomography (CT), and multispectral optoacoustic tomography (MSOT) within a single nanoplatform. The chemically engineered complex is composed of bovine serum albumin as biocompatible matrix, superparamagnetic iron oxide as MRI and MPI agents, and optoradiopaque bismuth sulfide as CT and MSOT agents. We demonstrate here its use for high-resolution, real-time, and quantitative in vivo imaging of mesenchymal stem cells transplanted in mouse brain. This versatile nanocomplex may find applications for monitoring cell transfer and cell transplantation in vivo using multiple imaging approaches.

bioengineering↗

Detection of Aggressive Mesenchymal Glioblastoma by Mannose-Weighted CEST MRI

Glioblastoma (GBM) contain mesenchymal cancer stem cells that drive tumor aggressiveness and recurrence and exhibit aberrant glycosylation during proneural-to-mesenchymal transition. A comprehensive analysis of human GBM transcriptomic datasets revealed an upregulation of 13 genes involved in mannosylation. Histopathological staining of a tissue array representing 35 GBM cases revealed elevated mannose, correlating with increased expression of the mesenchymal marker CD44. Mannose-weighted chemical exchange saturation transfer magnetic resonance imaging (MANw CEST MRI) detected elevated mannose levels in aggressive mesenchymal GBM neurospheres in vitro and in vivo, but not in less aggressive non-mesenchymal phenotype. To establish causation, inhibiting the expression of the mannose binding lectins LMAN1/2 that regulate intracellular processing of mannosylated proteins decreased the glioma cell MANw CEST MRI signal. Our findings indicate that MANw CEST MRI can visualize high mannose levels in mesenchymal GBM cells, which may serve as a surrogate imaging biomarker for predicting and assessing tumor aggressiveness and recurrence.

cancer biology↗