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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creator | Gorskaya, Yu. F. Danilova, T. A. Mezentseva, M. V. Shapoval, I. M. Narovlyanskii, A. N. Nesterenko, V. G. |
description | 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. |
doi_str_mv | 10.1007/s10517-011-1288-x |
format | Article |
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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.</description><identifier>ISSN: 0007-4888</identifier><identifier>EISSN: 1573-8221</identifier><identifier>DOI: 10.1007/s10517-011-1288-x</identifier><identifier>PMID: 22238749</identifier><identifier>CODEN: BEXBAN</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Animals ; Antigens ; Antigens, Bacterial - immunology ; Biomedical and Life Sciences ; Biomedicine ; Bone marrow ; Cell Biology ; Cell Count ; Cells, Cultured ; Cytokines - genetics ; Cytokines - metabolism ; Fibroblasts - immunology ; Fibroblasts - metabolism ; Gene Expression ; Gene Expression Regulation - immunology ; Genes ; Immunization ; Immunology and Microbiology ; Interferon ; Internal Medicine ; Laboratory Medicine ; Mice ; Mice, Inbred CBA ; Pathology ; Primary Cell Culture ; RNA ; Salmonella typhimurium ; Salmonella typhimurium - immunology ; Spleen - cytology ; Spleen - immunology ; Stromal Cells - immunology ; Stromal Cells - metabolism ; Tumor necrosis factor ; Vaccination</subject><ispartof>Bulletin of experimental biology and medicine, 2011-06, Vol.151 (2), p.197-200</ispartof><rights>Springer Science+Business Media, Inc. 2011</rights><rights>COPYRIGHT 2011 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-13c089faabb5f6093316e8e200b813c9b89a007fc8fb0369a0709a77357e2cd73</citedby><cites>FETCH-LOGICAL-c501t-13c089faabb5f6093316e8e200b813c9b89a007fc8fb0369a0709a77357e2cd73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10517-011-1288-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10517-011-1288-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22238749$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gorskaya, Yu. F.</creatorcontrib><creatorcontrib>Danilova, T. A.</creatorcontrib><creatorcontrib>Mezentseva, M. V.</creatorcontrib><creatorcontrib>Shapoval, I. M.</creatorcontrib><creatorcontrib>Narovlyanskii, A. N.</creatorcontrib><creatorcontrib>Nesterenko, V. G.</creatorcontrib><title>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</title><title>Bulletin of experimental biology and medicine</title><addtitle>Bull Exp Biol Med</addtitle><addtitle>Bull Exp Biol Med</addtitle><description>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.</description><subject>Animals</subject><subject>Antigens</subject><subject>Antigens, Bacterial - immunology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bone marrow</subject><subject>Cell Biology</subject><subject>Cell Count</subject><subject>Cells, Cultured</subject><subject>Cytokines - genetics</subject><subject>Cytokines - metabolism</subject><subject>Fibroblasts - immunology</subject><subject>Fibroblasts - metabolism</subject><subject>Gene Expression</subject><subject>Gene Expression Regulation - immunology</subject><subject>Genes</subject><subject>Immunization</subject><subject>Immunology and Microbiology</subject><subject>Interferon</subject><subject>Internal Medicine</subject><subject>Laboratory Medicine</subject><subject>Mice</subject><subject>Mice, Inbred CBA</subject><subject>Pathology</subject><subject>Primary Cell Culture</subject><subject>RNA</subject><subject>Salmonella typhimurium</subject><subject>Salmonella typhimurium - immunology</subject><subject>Spleen - cytology</subject><subject>Spleen - immunology</subject><subject>Stromal Cells - immunology</subject><subject>Stromal Cells - metabolism</subject><subject>Tumor necrosis factor</subject><subject>Vaccination</subject><issn>0007-4888</issn><issn>1573-8221</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kt1u0zAcxSMEYmXwANwgCyTgJsUfTexcVmGMSUNU6riOnPSf1iOxM3-IlifksXBIYQwB8oVl-3eOdeyTJE8JnhOM-RtHcEZ4iglJCRUi3d9LZiTjLBWUkvvJDEcoXQghTpJHzl2PS5yTh8kJpZQJvihmybfSBO2RadF66ECrBq29Nb3s0MpCE6wzFpXQdQ4pjT6oBpDUG3S2Hyw4p4weleXBm89KAzoHDT_Aqx04uNWtrOqlPaAydD5EIdoEq_QWvVVtCxbi_Suwymwckq0Hiy76Pmj1VfrjBUsd9dHqi_I7tJ4jfxh2qo8eoY9nXm1Bu8fJgzYy8OQ4nyaf3p1dle_Ty4_nF-XyMm0yTHxKWINF0UpZ11mb44IxkoMAinEt4llRi0LGZ2ob0daY5XHBcSE5ZxkH2mw4O01eTb6DNTcBnK965ZqYVGowwVUFyckiW2Q4kq__SxLMRFYwikfT53-g1yZYHXNUgrMcc0pG6MUEbWUHldKt8VY2o2e1ZFlOc56xPFLzv1BxbKBXjdHQqrh_R_DyN8EOZOd3znRhfHx3FyQT2FjjnIW2GqZ_jUmqsY_V1Mcq9rEa-1jto-bZMVioe9j8UvwsYAToBLhhrATY2-T_dv0OU4TrNQ</recordid><startdate>20110601</startdate><enddate>20110601</enddate><creator>Gorskaya, Yu. 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F. ; Danilova, T. A. ; Mezentseva, M. V. ; Shapoval, I. M. ; Narovlyanskii, A. N. ; Nesterenko, V. 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F.</au><au>Danilova, T. A.</au><au>Mezentseva, M. V.</au><au>Shapoval, I. M.</au><au>Narovlyanskii, A. N.</au><au>Nesterenko, V. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Bulletin of experimental biology and medicine</jtitle><stitle>Bull Exp Biol Med</stitle><addtitle>Bull Exp Biol Med</addtitle><date>2011-06-01</date><risdate>2011</risdate><volume>151</volume><issue>2</issue><spage>197</spage><epage>200</epage><pages>197-200</pages><issn>0007-4888</issn><eissn>1573-8221</eissn><coden>BEXBAN</coden><abstract>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.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>22238749</pmid><doi>10.1007/s10517-011-1288-x</doi><tpages>4</tpages></addata></record> |
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subjects | Animals Antigens Antigens, Bacterial - immunology Biomedical and Life Sciences Biomedicine Bone marrow Cell Biology Cell Count Cells, Cultured Cytokines - genetics Cytokines - metabolism Fibroblasts - immunology Fibroblasts - metabolism Gene Expression Gene Expression Regulation - immunology Genes Immunization Immunology and Microbiology Interferon Internal Medicine Laboratory Medicine Mice Mice, Inbred CBA Pathology Primary Cell Culture RNA Salmonella typhimurium Salmonella typhimurium - immunology Spleen - cytology Spleen - immunology Stromal Cells - immunology Stromal Cells - metabolism Tumor necrosis factor Vaccination |
title | 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 |
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