AUTHOR=Konkova Marina , Abramova Margarita , Kalianov Andrey , Ershova Elizaveta , Dolgikh Olga , Umriukhin Pavel , Izhevskaya Vera , Kutsev Sergey , Veiko Natalia , Kostyuk Svetlana 

TITLE=Mesenchymal Stem Cells Early Response to Low-Dose Ionizing Radiation

JOURNAL=Frontiers in Cell and Developmental Biology

VOLUME=8

YEAR=2020

URL=https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2020.584497

DOI=10.3389/fcell.2020.584497

ISSN=2296-634X

ABSTRACT=<sec><title>Introduction</title><p>Mesenchymal stem cells (MSCs) are applied as the therapeutic agents, e.g., in the tumor radiation therapy.</p></sec><sec><title>Purpose of the Study</title><p>To evaluate the human adipose MSC early response to low-dose ionizing radiation (LDIR).</p></sec><sec><title>Materials and Methods</title><p>We investigated different LDIR (3, 10, and 50 cGy) effects on reactive oxygen species production, DNA oxidation (marker 8-oxodG), and DNA breaks (marker ɣ H2AX) in the two lines of human adipose MSC. Using reverse transcriptase–polymerase chain reaction, fluorescence-activated cell sorting, and fluorescence microscopy, we determined expression of genes involved in the oxidative stress development (<italic>NOX4</italic>), antioxidative response (<italic>NRF2</italic>), antiapoptotic and proapoptotic response (<italic>BCL2</italic>, <italic>BCL2A1</italic>, <italic>BCL2L1</italic>, <italic>BIRC2</italic>, <italic>BIRC3</italic>, and <italic>BAX1</italic>), in the development of the nuclear DNA damage response (DDR) (<italic>BRCA1</italic>, <italic>BRCA2</italic>, <italic>ATM</italic>, and <italic>P53</italic>). Cell cycle changes were investigated by genes transcription changes (<italic>CCND1</italic>, <italic>CDKN2A</italic>, and <italic>CDKN1A</italic>) and using proliferation markers KI-67 and proliferating cell nuclear antigen (PCNA).</p></sec><sec><title>Results</title><p>Fifteen to 120 min after exposure to LDIR in MSCs, transient oxidative stress and apoptosis of the most damaged cells against the background of the cell cycle arrest were induced. Simultaneously, DDR and an antiapoptotic response were found in other cells of the population. The 10-cGy dose causes the strongest and fastest DDR following cell nuclei DNA damage. The 3-cGy dose induces a less noticeable and prolonged response. The maximal low range dose, 50 cGy, causes a damaging effect on the MSCs.</p></sec><sec><title>Conclusion</title><p>Transient oxidative stress and the death of a small fraction of the damaged cells are essential components of the MSC population response to LDIR along with the development of DDR and antiapoptotic response. A scheme describing the early MSC response to LDIR is proposed.</p></sec>