Evidence map›Paper›PMID 41239465›Full record

ArticleStem cell research & therapy2025

Generation of hTERT-immortalized human mesenchymal stromal cells with optical and magnetic labels for in vivo transplantation and tracking.

Anna N Gabashvili, Daria D Namestnikova, Mikhail V Gulyaev, Irina B Pevzner, Alexey D Bocharnikov, Natalya A Alexandrushkina, Anastasiya V Ryabova, Maria V Efremova, Viktoria A Sarkisova, Tatiana V Tarasova and 3 more

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Anna N GabashviliProkhorov General Physics Institute of the Russian Academy of Sciences, Moscow, 119991, Russia.
Daria D NamestnikovaFederal Center of Brain Research and Neurotechnologies, Federal Medical-Biological Agency of Russia, Moscow, 117513, Russia.
Mikhail V GulyaevFaculty of Chemistry, Lomonosov Moscow State University, Moscow, 119991, Russia.
Irina B PevznerA.N. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, 119992, Russia.
Alexey D BocharnikovA.N. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, 119992, Russia.
Natalya A AlexandrushkinaMedical Research and Educational Institute, Centre for Regenerative Medicine, Lomonosov Moscow State University, Moscow, 119192, Russia.
Anastasiya V RyabovaProkhorov General Physics Institute of the Russian Academy of Sciences, Moscow, 119991, Russia.
Maria V EfremovaDepartment of Applied Physics, Eindhoven University of Technology, P.O. Box 513, Eindhoven, 5600 MB, The Netherlands.
Viktoria A SarkisovaBiology Faculty, Lomonosov Moscow State University, Moscow, 119234, Russia.
Tatiana V TarasovaPsychiatric Hospital No. 1 Named after N.A. Alexeev of the Department of Health of Moscow, Moscow, 117152, Russia.
Stepan S VodopyanovAlbert Einstein College of Medicine, New York City, 10461, USA.
Pavel I MakarevichMedical Research and Educational Institute, Centre for Regenerative Medicine, Lomonosov Moscow State University, Moscow, 119192, Russia.
Petr I NikitinProkhorov General Physics Institute of the Russian Academy of Sciences, Moscow, 119991, Russia. nikitin@kapella.gpi.ru.

Funding

Russian Science Foundation 25-12-00373
6 · The paper itself

Abstract

backgroundMesenchymal stem/stromal cells (MSCs) are the focus of increasing research as a potential therapeutic agent for a range of nervous system diseases, due to their unique capacity for self-renewal and differentiation. The subsequent tracking of cells post-transplantation into the organism is of pivotal significance, as it elucidates their fate, distribution, and enables the timely monitoring of any adverse effects. In the context of cell monitoring, the utilization of a non-toxic label that exhibits long-term stability is of paramount importance.

methodsA human immortalized MSCs cell line was engineered to express a green fluorescent protein (GFP) and bacterial nanocompartments (high-molecular-weight icosahedral capsid-like protein complexes) via lentiviral transduction. The obtained cells were characterized by inductively coupled plasma mass spectrometry (ICP-MS) and Perls staining as well as using the nonlinear magnetization method, confocal microscopy and flow cytometry. An animal study was conducted in Sprague-Dawley rats.

resultsIn this study, an immortalized human MSCs cell line with stable expression of a novel magnetic resonance (MR) reporter label was established for the first time. GFP was genetically produced for utilization as an optical tag. A nanocompartment of the bacterium Quasibacillus thermotolerans (Qt) was used as a carrier of the magnetic label. The Qt nanocompartment consists of a shell and a ferroxidase cargo protein. Ferroxidase provides the biomineralization of iron ions within the nanocompartment shell. As a result, ferric oxide nanoparticles are formed inside the encapsulin nanocompartments, which have T2-contrast properties and serve as genetically encoded labels for magnetic resonance imaging (MRI) and for quantification by the nonlinear magnetization method.

conclusionsThe experimental results indicate that the use of two complementary labels allows for the multimodal visualization of the derived cells post-transplantation into the rat brain striatum, which is promising for monitoring MSCs-based therapy.

Indexed as

Cell TrackingMesenchymal Stem CellsMesenchymal Stem Cell TransplantationTelomeraseAnimalsCell LineGreen Fluorescent ProteinsHumansMaleRatsRats, Sprague-DawleyGreen Fluorescent ProteinsTelomeraseTERT protein, humanCell tracking in vivoEncapsulinsMagnetic particle quantificationMRI visualizationMultimodal imagingStem cells

Identifiers

PMID41239465
PMCPMC12619327

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.