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Encapsulin based self‐assembling iron‐containing protein nanoparticles for stem cells mri visualization

  • Anna N. Gabashvili
  • , Stepan S. Vodopyanov
  • , Nelly S. Chmelyuk
  • , Viktoria A. Sarkisova
  • , Konstantin A. Fedotov
  • , Maria V. Efremova
  • , Maxim A. Abakumov (Corresponding author)

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Over the past decade, cell therapy has found many applications in the treatment of different diseases. Some of the cells already used in clinical practice include stem cells and CAR‐T cells. Compared with traditional drugs, living cells are much more complicated systems that must be strictly controlled to avoid undesirable migration, differentiation, or proliferation. One of the approaches used to prevent such side effects involves monitoring cell distribution in the human body by any noninvasive technique, such as magnetic resonance imaging (MRI). Long‐term tracking of stem cells with artificial magnetic labels, such as magnetic nanoparticles, is quite problematic because such labels can affect the metabolic process and cell viability. Additionally, the concentration of exogenous labels will decrease during cell division, leading to a corresponding decrease in signal intensity. In the current work, we present a new type of genetically encoded label based on encapsulin from Myxococcus xanthus bacteria, stably expressed in human mesenchymal stem cells (MSCs) and coexpressed with ferroxidase as a cargo protein for nanoparticles’ synthesis inside encapsulin shells. mZip14 protein was expressed for the enhancement of iron transport into the cell. Together, these three proteins led to the synthesis of iron‐containing nanoparticles in mesenchymal stem cells—without affecting cell viability—and increased contrast properties of MSCs in MRI.

Original languageEnglish
Article number12275
Number of pages12
JournalInternational Journal of Molecular Sciences
Volume22
Issue number22
DOIs
Publication statusPublished - 12 Nov 2021
Externally publishedYes

Bibliographical note

Funding Information:
Funding: This research was funded by RSF grant number 19‐45‐06302. M.V.E. gratefully acknowl‐ edges the support of the Humboldt Research Fellowship for Postdoctoral Researchers provided by the Alexander von Humboldt Foundation and the support of the Add‐on Fellowship for Interdisci‐ plinary Life Science provided by the Joachim Herz Foundation.

Funding

Funding: This research was funded by RSF grant number 19‐45‐06302. M.V.E. gratefully acknowl‐ edges the support of the Humboldt Research Fellowship for Postdoctoral Researchers provided by the Alexander von Humboldt Foundation and the support of the Add‐on Fellowship for Interdisci‐ plinary Life Science provided by the Joachim Herz Foundation. This research was funded by RSF grant number 19?45?06302. M.V.E. gratefully acknowledges the support of the Humboldt Research Fellowship for Postdoctoral Researchers provided by the Alexander von Humboldt Foundation and the support of the Add?on Fellowship for Interdisciplinary Life Science provided by the Joachim Herz Foundation.Plasmids encoding EncA, B, C, D, and mZip14 genes were provided by Prof. Dr. Gil G. Westmeyer in the frame of the Helmholtz?RSF Joint Research Groups funding program (RSF 19?45?06302, HRSF?0064).

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Cell tracking
  • Encapsulins
  • Magnetic resonance imaging

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