Count of Splenic Stromal Precursor Cells in Mice and Expression of Cytokine Genes in These Cells in Primary Cultures during Different Periods after Immunization of Animals with S. typhimurium Antigens
Injection of S. typhimurium antigens signifi cantly (9-fold) increased cloning effi ciency and, hence, the content of stromal precursor cells in the spleen as soon as after 24 h. These parameters returned to normal by days 6–15 after immunization. Cultured splenocytes collected from immune (but not...
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Veröffentlicht in: | Bulletin of experimental biology and medicine 2011-06, Vol.151 (2), p.197-200 |
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Sprache: | eng |
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Zusammenfassung: | Injection of
S. typhimurium
antigens signifi cantly (9-fold) increased cloning effi ciency and, hence, the content of stromal precursor cells in the spleen as soon as after 24 h. These parameters returned to normal by days 6–15 after immunization. Cultured splenocytes collected from immune (but not intact) animals expressed the genes of proinfl ammatory cytokines IL-1β (on days 1, 6, 15) and IL-6 (on days 1 and 6), TNF-α (on days 6 and 15), and of IFN-α and IL-18 (on days 6 and 15). The expression of IL-4 gene was suppressed on day 6 after immunization, of IL-10 gene on days 1 and 6, of IL-6 gene on day 15. Hence, no signs of immune response suppression by stromal cells were found in this system. The spectrum and dynamics of the expression of pro- and anti-infl ammatory cytokine genes in stromal cell cultures from the spleen of immunized mice seemed to correspond to those needed for support of the immune response to
S. typhimurium
antigens, observed in immunized animals. The results indicate possible involvement of stromal cells in the realization of immune response
in vivo
. The increase of stromal precursor cells cloning effi ciency in response to antigen injection could not be reproduced
in vitro
: the presence of
S. typhimurium
antigens in primary cultures of intact mouse bone marrow and spleen throughout the entire period of culturing ~20-fold reduced cloning effi ciency in cultures. |
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ISSN: | 0007-4888 1573-8221 |
DOI: | 10.1007/s10517-011-1288-x |