Visualizing stem cells in vivo using magnetic resonance imaging

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2022 Mar;14(2):e1760. doi: 10.1002/wnan.1760. Epub 2021 Oct 15.

Abstract

Stem cell (SC) therapies displayed encouraging efficacy and clinical outcome in various disorders. Despite this huge hype, clinical translation of SC therapy has been disheartening due to contradictory results from clinical trials. The ability to monitor migration and engraftment of cells in vivo represents an ideal strategy in cell therapy. Therefore, suitable imaging approach to track MSCs would allow understanding of migratory and homing efficiency, optimal route of delivery and engraftment of cells at targeted location. Hence, longitudinal tracking of SCs is crucial for the optimization of treatment parameters, leading to improved clinical outcome and translation. Magnetic resonance imaging (MRI) represents a suitable imaging modality to observe cells non-invasively and repeatedly. Tracking is achieved when cells are incubated prior to implantation with appropriate contrast agents (CA) or tracers which can then be detected in an MRI scan. This review explores and emphasizes the importance of monitoring the distribution and fate of SCs post-implantation using current contrast agents, such as positive CAs including paramagnetic metals (gadolinium), negative contrast agents such as superparamagnetic iron oxides and 19 F containing tracers, specifically for the in vivo tracking of MSCs using MRI. This article is categorized under: Diagnostic Tools > In Vivo Nanodiagnostics and Imaging Nanotechnology Approaches to Biology > Nanoscale Systems in Biology Therapeutic Approaches and Drug Discovery > Emerging Technologies.

Keywords: 19F tracers; cell tracking; contrast agents; longitudinal; magnetic resonance imaging (MRI); mesenchymal; stem cells; superparamagnetic iron oxides (SPIO).

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Tracking / methods
  • Contrast Media
  • Magnetic Resonance Imaging / methods
  • Magnetite Nanoparticles*
  • Mesenchymal Stem Cells* / pathology
  • Stem Cells

Substances

  • Contrast Media
  • Magnetite Nanoparticles