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Magnetic resonance imaging of human neural stem cells in rodent and primate brain.

Lisa M McGinley | Matthew S Willsey | Osama N Kashlan | Kevin S Chen | John M Hayes | Ingrid L Bergin | Shayna N Mason | Aaron W Stebbins | Jacquelin F Kwentus | Crystal Pacut | Jennifer Kollmer | Stacey A Sakowski | Caleb B Bell | Cynthia A Chestek | Geoffrey G Murphy | Parag G Patil | Eva L Feldman
Stem cells translational medicine | 2021

Stem cell transplantation therapies are currently under investigation for central nervous system disorders. Although preclinical models show benefit, clinical translation is somewhat limited by the absence of reliable noninvasive methods to confirm targeting and monitor transplanted cells in vivo. Here, we assess a novel magnetic resonance imaging (MRI) contrast agent derived from magnetotactic bacteria, magneto-endosymbionts (MEs), as a translatable methodology for in vivo tracking of stem cells after intracranial transplantation. We show that ME labeling provides robust MRI contrast without impairment of cell viability or other important therapeutic features. Labeled cells were visualized immediately post-transplantation and over time by serial MRI in nonhuman primate and mouse brain. Postmortem tissue analysis confirmed on-target grft location, and linear correlations were observed between MRI signal, cell engraftment, and tissue ME levels, suggesting that MEs may be useful for determining graft survival or rejection. Overall, these findings indicate that MEs are an effective tool for in vivo tracking and monitoring of cell transplantation therapies with potential relevance to many cellular therapy applications.

Pubmed ID: 32841522

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: P30 CA046592
  • Agency: NINDS NIH HHS, United States
    Id: T32 NS007222
  • Agency: NCATS NIH HHS, United States
    Id: R43 TR001202
  • Agency: NINDS NIH HHS, United States
    Id: R25 NS089450
  • Agency: NIDDK NIH HHS, United States
    Id: P60 DK020572
  • Agency: NIA NIH HHS, United States
    Id: R01 AG052934
  • Agency: NIA NIH HHS, United States
    Id: U01 AG057562

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