PLOS ONE
PLOS ONE
a year ago

Immunoregulatory properties of erythroid nucleated cells induced from CD34+ progenitors from bone marrow

Immunoregulatory properties of erythroid nucleated cells induced from CD34+ progenitors from bone marrow
Julia A. Shevchenko, Roman Yu Perik-Zavodskii, Kirill V. Nazarov, Vera V. Denisova, Olga Yu. Perik-Zavodskaya, Yulia G. Philippova, Alaa Alsalloum, Sergey V. Sennikov
CD 71+ erythroid nucleated cells have pronounced immunoregulatory properties in normal and pathological conditions. Many populations of cells with immunoregulatory properties are considered candidates for cellular immunotherapy for various pathologies. This study characterized the immunoregulatory properties of CD71+ erythroid cells derived from CD34-positive bone marrow cells under the influence of growth factors that stimulate differentiation into erythroid cells. CD34-negative bone marrow cells were used to isolate CD71+ erythroid nuclear cells. The resulting cells were used to assess the phenotype, determine the mRNA spectrum of the genes responsible for the main pathways and processes of the immune response, and obtain culture supernatants for the analysis of immunoregulatory factors. It was found that CD71+ erythroid cells derived from CD34+ cells carry the main markers of erythroid cells, but differ markedly from natural bone marrow CD71+ erythroid cells. The main differences are in the presence of the CD45+ subpopulation, distribution of terminal differentiation stages, transcriptional profile, secretion of certain cytokines, and immunosuppressive activity. The properties of induced CD71+ erythroid cells are closer to the cells of extramedullary erythropoiesis foci than to natural bone marrow CD71+ erythroid cells. Thus, when cultivating CD71+ erythroid cells for clinical experimental studies, it is necessary to take into account their pronounced immunoregulatory activity.

Publisher URL: https://journals.plos.org/plosone/article

Open URL: https://doi.org/10.1371/journal.pone.0287793

DOI: 10.1371/journal.pone.0287793

Open access
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