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Effects of exposure to gradient magnetic fields emitted by nuclear magnetic resonance devices on clonogenic potential and proliferation of human hematopoietic stem cells

TitleEffects of exposure to gradient magnetic fields emitted by nuclear magnetic resonance devices on clonogenic potential and proliferation of human hematopoietic stem cells
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2016
AuthorsIachininoto, M.G., Camisa V., Leone L., Pinto Rosanna, Lopresto Vanni, Merla Caterina, Giorda E., Carsetti R., Zaffina S., Podda M.V., Teofili L., and Grassi C.
JournalBioelectromagnetics
Volume37
Pagination201-211
ISSN01978462
Keywordsadult, adverse effects, Antigens, CD34, CD34 antigen, CFU counting, Colony-Forming Units Assay, cytology, devices, erythroid cell, Erythroid Cells, hematopoietic stem cell, Hematopoietic Stem Cells, human, Humans, magnetic field, Magnetic fields, Magnetic Resonance Spectroscopy, male, metabolism, Middle Aged, monocyte, Monocytes, Nuclear magnetic resonance spectroscopy
Abstract

This study investigates effects of gradient magnetic fields (GMFs) emitted by magnetic resonance imaging (MRI) devices on hematopoietic stem cells. Field measurements were performed to assess exposure to GMFs of staff working at 1.5 T and 3 T MRI units. Then an exposure system reproducing measured signals was realized to expose in vitro CD34+ cells to GMFs (1.5 T-protocol and 3 T-protocol). CD34+ cells were obtained by Fluorescence Activated Cell Sorting from six blood donors and three MRI-exposed workers. Blood donor CD34+ cells were exposed in vitro for 72h to 1.5 T or 3 T-protocol and to sham procedure. Cells were then cultured and evaluated in colony forming unit (CFU)-assay up to 4 weeks after exposure. Results showed that in vitro GMF exposure did not affect cell proliferation but instead induced expansion of erythroid and monocytes progenitors soon after exposure and for the subsequent 3 weeks. No decrease of other clonogenic cell output (i.e., CFU-granulocyte/erythroid/macrophage/megakaryocyte and CFU-granulocyte/macrophage) was noticed, nor exposed CD34+ cells underwent the premature exhaustion of their clonogenic potential compared to sham-exposed controls. On the other hand, pilot experiments showed that CD34+ cells exposed in vivo to GMFs (i.e., samples from MRI workers) behaved in culture similarly to sham-exposed CD34+ cells, suggesting that other cells and/or microenvironment factors might prevent GMF effects on hematopoietic stem cells in vivo. Accordingly, GMFs did not affect the clonogenic potential of umbilical cord blood CD34+ cells exposed in vitro together with the whole mononuclear cell fraction. © 2016 Wiley Periodicals, Inc.

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URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84961266593&doi=10.1002%2fbem.21967&partnerID=40&md5=a330a44b4f1133c00be36f5714a10b57
DOI10.1002/bem.21967
Citation KeyIachininoto2016201