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World J Plast Surg. 2017 January; 6(1): 111–113.
PMCID: PMC5339619

The Regenerative Effect of Bone Marrow-Derived Stem Cells on Cell Count and Survival in Acute Radiation Syndrome

DEAR EDITOR

Acute radiation syndrome (ARS) is called as radiation sickness or radiation toxicity caused by abnormally high exposure to ionizing radiation in a very short period of time.1 High doses of ionizing radiation are able to contribute to detrimental systemic effects in different organs.2 In treatment of patients with ARS, physicians have used growth factors, cytokines and bone marrow transplantation.3 Mesenchymal stem cells (MSCs) have the potential for multilineage differentiation.4,5 Bone marrow-derived stem cells (BMSCs) are the most well- known type of the mesenchymal stem cells used with safety and efficacy in several diseases such as ARS.1 The present study assessed the regenerative effect of bone marrow-derived stem cells on cell count and survival in Acute Radiation Syndrome.

For MSC culture, both femoral and tibial bones from male mice were removed and after removal of muscular and connective tissues, the bones were cut at both ends and the bone marrow was flushed out into a 15 ml falcon tube filled with Dulbecco’s Modified Eagle Medium (DMEM; Biovet, Bulgaria) and 1% penicillin streptomycin (Sigma, USA) and centrifuged at 1200 rpm for 5 minutes. The precipitate was cultured in 25 cm2 flasks containing DMEM supplemented with 10% fetal bovine serum (FBS; Biovet, Bulgaria), 1% L-glutamine (Sigma, USA) and 1% penicillin and streptomycin. The culture flasks were transferred into CO2 incubator while the medium was changed every 3 days.

The adherent cells were subcultured until passage 5 while they were counted for survival rate. The osteogenic was evaluated with Alizarin Red staining (Sigma, USA). RT-PCR was conducted to evaluate the expression of MSC markers. Forty 8-12 weeks male mice were randomly divided into 2 equal groups. Group A received no BMSCs but group B underwent 150×103 cells of passage 5 in 150 µl medium of BMSC transplantation intravenously into the tail, 24 hours after γ irradiation. Both groups were irradiated with 10 Gy (dose rate .286 Gy/ min) 60CO, during 35 minutes with a field size of 35×35 for all the body area.

BMSCs were plastic adherent and spindle-shape (Figure 1) and expressed CD90 marker but not CD34 and CD45 (Figure 2). Culture of BMSCs in osteogenic media lead to osteogenic differentiation of these cells (Figure 3). A significant increase was noticed for the number cells in bone marrow in group B when compared to group A, one week after γ irradiation (p=0.0001, Table 1). The mortality rate one and two weeks after γ irradiation was demonstrated in Table 2.

Fig. 1
Bone marrow-derived stem cells in 3rd passage
Fig. 2
RT-PCR with positive expression of CD90 and absence of CD34 and CD45 (Ladder, CD90, CD34, 3: CD45
Fig. 3
Alizarin red staining with osteogenic differentiation of bone marrow-derived stem cells
Table 1
Cell count in bone marrow one week after γ irradiation
Table 2
Mortality rate one and two weeks after γ irradiation

BMSCs were shown to differentiate into various cells, and secrete cytokine and growth factors, and have immunomodulatory properties through paracrine and endocrine mechanisms in injured tissue.6 Eaton et al. showed that MSC therapy can be effective for acute radiation syndrome due to the fact that MSCs have immunomodulatory properties.7 Guo et al. in a 32-year-old man who was exposed to whole body dose of 14.5 GY γ- radiation concluded that cell therapy was an effective approach and significantly decreased mortality rate.8 Lange et al. found that systemic administration of MSCs had healing effects in ARS and managed radiation.3 Chapel et al. revealed that MSCs can migrate to the site of injury and repair the injured tissue.9 The therapeutic use of compact of BMSCs was shown to reduce the injury and increase the survival rate after lethal whole body irradiation.10,11

These studies confirm our findings demonstrating that BMSCs reduced the detrimental effects of radiation and increased the survival rate in ARS. Based on our findings, BMSCs can be recommended in reduction of detrimental effects of ARS and decreasing the mortality after exposure to γ irradiation.

ACKNOWLEDGEMENTS

This work was supported by Stem Cell and Transgenic Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. Authors also wish thanks the support Leo E Gerweck.

CONFLICT OF INTEREST

The authors declare no conflict of interest.

References

1. Hu K, Sun Q, Guo M, Ai H. The radiation protection and therapy effects of mesenchymal stem cells in mice with acute radiation injury. Br J Radiol. 2010;83:52–8. [PMC free article] [PubMed]
2. Meineke V, Fliedner T. Radiation-induced multi-organ involvement and failure: challenges for radiation accident medical management and future research. Br J Radiol. 2014;27:196–200.
3. Lange C, Brunswig-Spickenheier B, Cappallo-Obermann H, Eggert K, Gehling UM, Rudolph C, Schlegelberger B, Cornils K, Zustin J, Spiess AN, Zander AR. Radiation rescue: mesenchymal stromal cells protect from lethal irradiation. PloS One. 2011;6:1–12. [PMC free article] [PubMed]
4. Girlovanu M, Susman S, Soritau O, Rus-Ciuca D, Melincovici C, Constantin AM, Mihu CM. Stem cells - biological update and cell therapy progress. Clujul Med. 2015;8:265–71. [PMC free article] [PubMed]
5. Mehrabani D, Mojtahed Jaberi F, Zakerinia M, Hadianfard MJ, Jalli R, Tanideh N, Zare Sh. The healing effect of bone marrow-derived stem cells in knee osteoarthritis: a case report. World J Plast Surg. 2016;5:164–170. [PMC free article] [PubMed]
6. Mehrabani D, Mehraban G, Zare S, Manafi A. Adipose-derived stem cells (ADSC) and aesthetic medicine: a mini review. World J Plast Surg. 2013;22:65–70. [PMC free article] [PubMed]
7. Eaton EB, Varney TR. Mesenchymal stem cell therapy for acute radiation syndrome: innovative medical approaches in military medicine. Mil Med Res. 2015;2:2–9. [PMC free article] [PubMed]
8. Guo M, Dong Z, Qiao J, Yu C, Sun Q, Hu K, Liu G, Wei L, Yao B, Man Q, Sun X, Liu Z, Song Z, Yu C, Chen Y, Luo Q, Liu S, Ai HS. Severe acute radiation syndrome: treatment of a lethally 60Co-source irradiated accident victim in China with HLA-mismatched peripheral blood stem cell transplantation and mesenchymal stem cells. J Radiat Res. 2013;55:205–9. [PMC free article] [PubMed]
9. Chapel A, Bertho JM, Bensidhoum M, Fouillard L, Young RG, Frick J, Demarquay C, Cuvelier F, Mathieu E, Trompier F, Dudoignon N, Germain C, Mazurier C, Aigueperse J, Borneman J, Gorin NC, Gourmelon P, Thierry D. Mesenchymal stem cells home to injured tissues when co-infused with hematopoietic cells to treat a radiation-induced multi-organ failure syndrome. J Gene Med. 2003;5:1028–38. [PubMed]
10. Shukai Q, Hanyun R, Yongjin S, Wei L. Allogeneic compact bone-derived mesenchymal stem cell transplantation increases survival of mice exposed to lethal total body irradiation: a potential immunological mechanism. Chin Med J. 2014;127:475–82. [PubMed]
11. Mortazavi SMJ, Shekoohi-Shooli F, Aghamir SMR, Mehrabani D, Dehghanian AR, Zare S, Mosleh-Shirazi MA. The healing effect of bone marrow-derived stem cells in acute radiation syndrome. Pak J Med Sci. 2016;32:1–6. [PubMed]

Articles from World Journal of Plastic Surgery are provided here courtesy of Iran Society of Plastic, Reconstructive and Aesthetic Surgeons