Effectiveness of cell therapy of acute radiation syndrome in mice with intravenous and intraperitoneal administration of a cellular product
- Authors: Murzina E.V.1, Pak N.V.1, Aksenova N.V.1, Zhirnova N.A.1, Veselova O.M.1, Khovpachev A.A.1, Belyj N.V.1
-
Affiliations:
- Kirov Military Medical Academy
- Issue: Vol 26, No 2 (2024)
- Pages: 169-184
- Section: Original Study Article
- URL: https://journals.rcsi.science/1682-7392/article/view/267233
- DOI: https://doi.org/10.17816/brmma609492
- ID: 267233
Cite item
Abstract
The therapeutic effect of fibroblast-like cells obtained from the stromal vascular fraction of subcutaneous adipose tissue of mice and cultured for the treatment of bone marrow form of acute radiation syndrome was studied on a mouse experimental model. The cells were identified as multipotent mesenchymal stem (stromal) cells, owing to adhesion to plastic, confluent monolayer formation during cultivation, and the fact that osteogenic differentiation in vitro resulted in osteoblast maturation and calcium deposit formation, which indicated their multipotent nature. Irradiation of laboratory rodents was conducted using the X-ray therapy unit “RUM-17”. Stromal cells were obtained from subcutaneous adipose tissue of a mouse and grown in a culture of 3–4 passages and used as a cell product. Cell transplantation was performed 24 h after uniform X-ray irradiation of mice at a dose of 7.8 Gy. This is the first study to compare the therapeutic efficacy of allogeneic transplantation of multipotent mesenchymal stem cells with the different routes (intravenous and intraperitoneal) of cell suspension administration. A significant increase was found in the survival rate of mice during the 30-day follow-up period after lethal dose irradiation, which depended on the number of injected cells and delivery method of the biomedical cell product. Thus, with intravenous administration of 30 and 60 × 103 multipotent mesenchymal stem cells, the 30-day survival rate of mice after irradiation at a dose of 7.8 Gy increased by 54.5% and 40%, respectively, compared with that of untreated animals (p = 0.03). An increase in the number of cells in the cell product to 120 × 103/mouse led to a decrease in therapy effectiveness. In intraperitoneal administration, the protection of animals from death was 57% after transplantation of 30 and 60 × 103 cells (p = 0.039) and 50% after application of 120 × 103 cells. On day 30 after irradiation, in the introduction of a cellular product in different schemes, 70%–80% of animals showed restoration of the values of the main indicators of the hematopoiesis system to initial levels. Thus, cell therapy using multipotent mesenchymal stem cells isolated from adipose tissue with intravenous and intraperitoneal delivery routes of the cellular product to the irradiated body protects mice from death after exposure to X-ray radiation in lethal doses, decreasing the severity of radiation damage to the hematopoietic system in mice, and provides prospects for further research as an effective and safe treatment for acute radiation sickness.
Full Text
##article.viewOnOriginalSite##About the authors
Elena V. Murzina
Kirov Military Medical Academy
Author for correspondence.
Email: elenmurzina@mail.ru
ORCID iD: 0000-0001-7052-3665
SPIN-code: 5188-0797
MD, Cand. Sci. (Biol.)
Russian Federation, Saint PetersburgNatalya V. Pak
Kirov Military Medical Academy
Email: elenmurzina@mail.ru
ORCID iD: 0000-0003-1239-5663
SPIN-code: 7181-3780
MD, Cand. Sci. (Biol.)
Russian Federation, Saint PetersburgNatalia V. Aksenova
Kirov Military Medical Academy
Email: elenmurzina@mail.ru
ORCID iD: 0000-0002-5645-7072
SPIN-code: 6821-6887
MD, Cand. Sci. (Med.)
Russian Federation, Saint PetersburgNatalya A. Zhirnova
Kirov Military Medical Academy
Email: elenmurzina@mail.ru
ORCID iD: 0000-0002-9948-6260
SPIN-code: 8308-2139
MD, Cand. Sci. (Biol.)
Russian Federation, Saint PetersburgOlga M. Veselova
Kirov Military Medical Academy
Email: elenmurzina@mail.ru
ORCID iD: 0009-0007-9345-1845
SPIN-code: 4864-8391
researcher
Russian Federation, Saint PetersburgAleksej A. Khovpachev
Kirov Military Medical Academy
Email: khovpachev@gmail.com
ORCID iD: 0009-0002-5780-1557
SPIN-code: 6189-3624
MD, Cand. Sci. (Med.)
Russian Federation, Saint PetersburgNikolaj V. Belyj
Kirov Military Medical Academy
Email: elenmurzina@mail.ru
ORCID iD: 0000-0002-9370-8678
SPIN-code: 8676-3186
clinical laboratory diagnostics doctor
Russian Federation, Saint PetersburgReferences
- Merkulov VA, Bunyatyan ND, Radaev SM. Problems and perspectives of cell therapy in clinical practice. Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products. Regulatory Research and Medicine Evaluation. 2011;(2):35–38. EDN: RWVTFZ
- Moskalev AB, Gumileskiy BYu, Apchel AV, Tsygan VN. Stem cells and their physiological effects. Bulletin of the Russian Military Medical Academy. 2019;68(4):172–180. EDN: ZBDYZF
- Qian L, Cen J. Hematopoietic stem cells and mesenchymal stromal cells in acute radiation syndrome. Oxid Med Cell Longev. 2020;2020:8340756. doi: 10.1155/2020/8340756
- Singh VK, Seed TM. Pharmacological management of ionizing radiation injuries: current and prospective agents and targeted organ systems. Expert Opin Phamacother. 2020;21(3):317–337. doi: 10.1080/14656566.2019.1702968
- Vlasenko AN, Gaiduk SV, Legeza VI, et al. Clinical radiology. Saint Petersburg: Foliant; 2020. 448 p. (In Russ.)
- Samoylov AS, Konchalovsky MV, Bushmanov Ayu, et al. Recommendations for the diagnosis and treatment of bone marrow form of acute radiation syndrome. Gematologiya i transfuziologiya. 2023;68(1):98–128. EDN: NONQCI doi: 10.35754/0234-5730-2023-68-1-98-12
- Asano S. Current status of hematopoietic stem cell transplantation for acute radiation syndromes. Int J Hematol. 2012;95(3):227–231. doi: 10.1007/s12185-012-1027-8
- Kalmykova NV, Alexandrova SV. Therapeutic effects of multipotent mesenchymal stromal cells after irradiation. Radiation biology. Radioecology. 2016;56(2):117–137. EDN: VVHLHR doi: 10.7868/S0869803116020077
- Rezvani M. Therapeutic potential of mesenchymal stromal cells and extracellular vesicles in the treatment of radiation lesions — a review. Cells. 2021;10(2):427. doi: 10.3390/cells10020427
- Potapnev MP. Analysis of approaches to increase the efficacy of cell therapy based on mesenchymal stromal cells. Genes & Cells. 2021;16(4):22–28. EDN: FWMWHS doi: 10.23868/202112003
- Directive 2010/63/EU of the European parliament and of the council of 22 September 2010 on the protection of animals used for scientific purposes (Text with EEA relevance). Official Journal of the European Union. 2010:33–79. (In Russ.)
- Zuk PA, Zhu M, Ashjian P. Human adipose tissue is a source of multipotent stem cells. Mol Biol Cell. 2002;13(12):4279–4295. doi: 10.1091/mbc. E02–02–0105
- Dominici M, Le Blanc K, Mueller I, et al. Minimal criteria for defining multipotent mesenchymal stromal cells. Cytotherapy. 2006;8(4):315–317. doi: 10.1080/14653240600855905
- Vasil’ev VS, Manturova NE, Vasil’ev SA, Teryushkova ZhI. Biological features of adipose tissue. Plastic Surgery and Aesthetic Medicine. 2019;2:33–42. EDN: FFFVTP doi: 10.17116/plast.hirurgia201902133
- Bandekar M, Maurya DK, Sharma D, Sandur SK. Preclinical studies and clinical prospects of Wharton’s Jelly-derived MSC for treatment of acute radiation syndrome. Curr Stem Cell Rep. 2021;7(2):85–94. doi: 10.1007/s40778-021-00188-4
- Kovalenko OA, Azzam EI, Ende N. Human umbilical cord blood mononucleated cells enhance the survival of lethally irradiated mice: dosage and the window of time. J Radiat Res. 2013;54(6):1010–1014. doi: 10.1093/jrr/rrt062
- Lee RH, Pulin AA, Seo MJ, et al. Intravenous hMSCs improve myocardial infarction in mice because cells embolized in lung are activated to secrete the anti-inflammatory protein TSG-6. Cell Stem Cell. 2009;5(1):54–63. doi: 10.1016/j.stem.2009.05.003
- Schmuck EG, Koch JM, Centanni JM, et al. Biodistribution and clearance of human mesenchymal stem cells by quantitative three-dimensional cryoimaging after intravenous infusion in a rat lung injury model. Stem Cells Transl Med. 2016;5(12):1668–1675. doi: 10.5966/sctm.2015-0379
- Payushina OV, Tsomartova DA, Chereshneva YV., et al. Regulatory effects of mesenchymal stromal cells on the development of liver fibrosis: Cellular and molecular mechanisms and prospects of clinical application. Journal of General Biology. 2020;81(1):83–95. doi: 10.31857/S0044459620020062
- Chinnapaka S, Yang KS, Samadi Y, et al. Allogeneic adipose-derived stem cells mitigate acute radiation syndrome by the rescue of damaged bone marrow cells from apoptosis. Stem Cells J. 2021;10(7):1095–1114. doi: 10.1002/sctm.20-0455
- Pinzur L, Akyuez L, Levdansky L, et al. Rescue from lethal acute radiation syndrome (ARS) with severe weight loss by secretome of intramuscularly injected human placental stromal cells. J Cachexia Sarcopenia Muscle. 2018;9(6):1079–1092. doi: 10.1002/jcsm.12342
- Maiborodin IV, Maslov RV, Mikheeva TV, et al. The distribution of multipotent mesenchymal stromal cells and their detritus throughout the organism after subcutaneous introduction. Journal of General Biology. 2020;81(1):96–107. EDN: JPTPXD doi: 10.31857/S0044459620020050
- Hu KX, Sun QY, Guo M, Ai HS. The radiation protection and therapy effects of mesenchymal stem cells in mice with acute radiation injury. British J Rad. 2010;83(985):52–58. doi: 10.1259/bjr/61042310
Supplementary files
