Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/3870
Title: Evaluation of the Biodistribution of Mesenchymal Stem Cells in a Pre-clinical Renal Tuberculosis Model by Non-linear Magnetic Response Measurements
Authors: Nayak, Barsa
Sonavane, Avinash
Issue Date: 2021
Publisher: Frontiers Media S.A.
Citation: Yudintceva, N., Mikhailova, N., Bobkov, D., Yakovleva, L., Nikolaev, B., Krasavina, D., . . . Shevtsov, M. (2021). Evaluation of the biodistribution of mesenchymal stem cells in a pre-clinical renal tuberculosis model by non-linear magnetic response measurements. Frontiers in Physics, 9 doi:10.3389/fphy.2021.625622
Abstract: Bone-marrow derived mesenchymal stem cells (MSCs) exert anti-tuberculosis effects due to their potential to repair damaged tissues and modulate inflammatory immune responses. MSCs were reported to be recruited to the Mycobacterium tuberculosis (Mtb) affected sites in the organism. However, due to limitations of presently applied in vivo imaging techniques the trafficking and biodistribution of MSCs in Mtb-infected organisms is not possible. In the current study MSCs were labeled with superparamagnetic iron oxide nanoparticles (SPIONs) as a negative MR contrast agent for imaging the biodistribution of MSCs in vivo. Trafficking of SPIONs-labeled MSCs was analyzed in a preclinical model of renal tuberculosis in male Chinchilla rabbits (n = 18) following intravenous administration on the days 0, 2, 3, and 7 employing a highly sensitive method of non-linear longitudinal magnetic response (NLR-M2) measurements. Within 48 h after injection, nanoparticle-labeled MSCs accumulated predominantly in lung, spleen, liver tissues, and paratracheal lymph nodes with subsequent decrease over the observation period of 7 days. The recruitment of MSCs to Mtb-affected organs was further proven by immunohistological analysis. NLR-M2 allowed the detection of SPIONs-labeled cells at low concentrations in different organs and tissues giving insights of in vivo mesenchymal stem cells trafficking in organism after TB infection. © Copyright © 2021 Yudintceva, Mikhailova, Bobkov, Yakovleva, Nikolaev, Krasavina, Muraviov, Vinogradova, Yablonskiy, Samusenko, Ryzhov, Deriglazov, Marchenko, Multhoff, Klapproth, Li, Nayak, Sonawane and Shevtsov.
URI: https://doi.org/10.3389/fphy.2021.625622
https://dspace.iiti.ac.in/handle/123456789/3870
ISSN: 2296-424X
Type of Material: Journal Article
Appears in Collections:Department of Biosciences and Biomedical Engineering

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