In Situ Observation of Germinal Center Cell Apoptosis During a Secondary Immune Response
Germinal centers are highly organized anatomic structures essential for the clonal expansion of germinal center (GC) B-cells and associated somatic hypermutation, isotype switching, selection of the high-affinity B-cells (affinity maturation), and elimination of irrelevant or autoreactive clones. Th...
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Veröffentlicht in: | Journal of Clinical and Experimental Hematopathology 2006, Vol.46(2), pp.73-82 |
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creator | Saitoh, Hito-aki Maeda, Kunihiko Yamakawa, Mitsunori |
description | Germinal centers are highly organized anatomic structures essential for the clonal expansion of germinal center (GC) B-cells and associated somatic hypermutation, isotype switching, selection of the high-affinity B-cells (affinity maturation), and elimination of irrelevant or autoreactive clones. The identification of cellular interactions and regulatory mechanisms controlling apoptosis within GCs is essential for a complete understanding of the cellular and molecular dynamics of the GC reaction. We performed a kinetic analysis of the apoptotic activity occurring within GCs of draining lymph nodes of mice immunized with sheep red blood cells (SRBC) after secondary stimulation. The apoptotic activity of GC cells can be divided into three distinct phases : 1) initial phase (within the first days after immunization), 2) reactive phase (from the 5th day to 15th day after secondary immunization), and 3) late phase (after the 15th day). Apoptosis decreased shortly after secondary immunization followed by an increase to peak after an additional 10 days. Finally, apoptosis of GC cells decreased to basal levels. Administration of apoptosis inhibitors decreased the amount of apoptosis during the reactive phase. These results suggest that the reactive phase may be the critical period in which clonal selection and cellular differentiation to antibody forming cells take place. [J Clin Exp Hematopathol 46(2) : 73-82, 2006] |
doi_str_mv | 10.3960/jslrt.46.73 |
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The identification of cellular interactions and regulatory mechanisms controlling apoptosis within GCs is essential for a complete understanding of the cellular and molecular dynamics of the GC reaction. We performed a kinetic analysis of the apoptotic activity occurring within GCs of draining lymph nodes of mice immunized with sheep red blood cells (SRBC) after secondary stimulation. The apoptotic activity of GC cells can be divided into three distinct phases : 1) initial phase (within the first days after immunization), 2) reactive phase (from the 5th day to 15th day after secondary immunization), and 3) late phase (after the 15th day). Apoptosis decreased shortly after secondary immunization followed by an increase to peak after an additional 10 days. Finally, apoptosis of GC cells decreased to basal levels. Administration of apoptosis inhibitors decreased the amount of apoptosis during the reactive phase. These results suggest that the reactive phase may be the critical period in which clonal selection and cellular differentiation to antibody forming cells take place. 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The identification of cellular interactions and regulatory mechanisms controlling apoptosis within GCs is essential for a complete understanding of the cellular and molecular dynamics of the GC reaction. We performed a kinetic analysis of the apoptotic activity occurring within GCs of draining lymph nodes of mice immunized with sheep red blood cells (SRBC) after secondary stimulation. The apoptotic activity of GC cells can be divided into three distinct phases : 1) initial phase (within the first days after immunization), 2) reactive phase (from the 5th day to 15th day after secondary immunization), and 3) late phase (after the 15th day). Apoptosis decreased shortly after secondary immunization followed by an increase to peak after an additional 10 days. Finally, apoptosis of GC cells decreased to basal levels. Administration of apoptosis inhibitors decreased the amount of apoptosis during the reactive phase. These results suggest that the reactive phase may be the critical period in which clonal selection and cellular differentiation to antibody forming cells take place. [J Clin Exp Hematopathol 46(2) : 73-82, 2006]</description><subject>Animals</subject><subject>apoptosis</subject><subject>Apoptosis - immunology</subject><subject>B-Lymphocytes - immunology</subject><subject>Female</subject><subject>follicular dendritic cell</subject><subject>Germinal Center - cytology</subject><subject>Germinal Center - immunology</subject><subject>germinal center B-cell</subject><subject>Immunization, Secondary</subject><subject>Immunohistochemistry</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>mouse lymph node</subject><subject>secondary immune response</subject><issn>1346-4280</issn><issn>1880-9952</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM1v1DAQxSMEoqVw4o584oKy-DvJjWoLy0qVKlGQuFmOM2m9cuxgO5X63-NtFnrwjKX5-c3zq6r3BG9YJ_HnQ3Ixb7jcNOxFdU7aFtddJ-jLcmdc1py2-Kx6k9IBYy6FZK-rM9IQTjvRnFe_9x7d2rygmz5BfNDZBo_CiHYQJ-u1Q1vwGWJpzqHLOcw5JJvQ1RKtv0Ma3YIJftDxEe2nafGAfkCag0_wtno1apfg3alfVL--ff25_V5f3-z228vr2oiO5lozBhSTxhCJiRBM9gPXLWl6UwyOxaaAHrCUtOcd16Zl7Tg0cmDaYEY76NhF9XHVnWP4s0DKarLJFLfaQ1iSki0lTEpSwE8raGJIKcKo5min4lwRrI5BqqcgFZeqYYX-cJJd-gmGZ_aUXAF2K1Cm1mgXvLMe1CEsscSWlAmte5zme0UxluoYPabHVk7DSim2cCMEP_7gy6p0SFnfwf9VOmZrHDzbomspz_-NzL2OCjz7Cx_pnN0</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Saitoh, Hito-aki</creator><creator>Maeda, Kunihiko</creator><creator>Yamakawa, Mitsunori</creator><general>The Japanese Society for Lymphoreticular Tissue Research</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2006</creationdate><title>In Situ Observation of Germinal Center Cell Apoptosis During a Secondary Immune Response</title><author>Saitoh, Hito-aki ; Maeda, Kunihiko ; Yamakawa, Mitsunori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c592t-a33e2017c16015536bd4a817bc429f7145ebe0662b494ac838fd76d3ac0329e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>apoptosis</topic><topic>Apoptosis - immunology</topic><topic>B-Lymphocytes - immunology</topic><topic>Female</topic><topic>follicular dendritic cell</topic><topic>Germinal Center - cytology</topic><topic>Germinal Center - immunology</topic><topic>germinal center B-cell</topic><topic>Immunization, Secondary</topic><topic>Immunohistochemistry</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>mouse lymph node</topic><topic>secondary immune response</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saitoh, Hito-aki</creatorcontrib><creatorcontrib>Maeda, Kunihiko</creatorcontrib><creatorcontrib>Yamakawa, Mitsunori</creatorcontrib><creatorcontrib>Yamagata University School of Medicine</creatorcontrib><creatorcontrib>Department of Pathology</creatorcontrib><creatorcontrib>Japan</creatorcontrib><creatorcontrib>Yamagata</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of Clinical and Experimental Hematopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saitoh, Hito-aki</au><au>Maeda, Kunihiko</au><au>Yamakawa, Mitsunori</au><aucorp>Yamagata University School of Medicine</aucorp><aucorp>Department of Pathology</aucorp><aucorp>Japan</aucorp><aucorp>Yamagata</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Situ Observation of Germinal Center Cell Apoptosis During a Secondary Immune Response</atitle><jtitle>Journal of Clinical and Experimental Hematopathology</jtitle><addtitle>J Clin Exp Hematopathol</addtitle><date>2006</date><risdate>2006</risdate><volume>46</volume><issue>2</issue><spage>73</spage><epage>82</epage><pages>73-82</pages><issn>1346-4280</issn><eissn>1880-9952</eissn><abstract>Germinal centers are highly organized anatomic structures essential for the clonal expansion of germinal center (GC) B-cells and associated somatic hypermutation, isotype switching, selection of the high-affinity B-cells (affinity maturation), and elimination of irrelevant or autoreactive clones. The identification of cellular interactions and regulatory mechanisms controlling apoptosis within GCs is essential for a complete understanding of the cellular and molecular dynamics of the GC reaction. We performed a kinetic analysis of the apoptotic activity occurring within GCs of draining lymph nodes of mice immunized with sheep red blood cells (SRBC) after secondary stimulation. The apoptotic activity of GC cells can be divided into three distinct phases : 1) initial phase (within the first days after immunization), 2) reactive phase (from the 5th day to 15th day after secondary immunization), and 3) late phase (after the 15th day). Apoptosis decreased shortly after secondary immunization followed by an increase to peak after an additional 10 days. Finally, apoptosis of GC cells decreased to basal levels. Administration of apoptosis inhibitors decreased the amount of apoptosis during the reactive phase. 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source | J-STAGE Free; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals apoptosis Apoptosis - immunology B-Lymphocytes - immunology Female follicular dendritic cell Germinal Center - cytology Germinal Center - immunology germinal center B-cell Immunization, Secondary Immunohistochemistry Mice Mice, Inbred BALB C mouse lymph node secondary immune response |
title | In Situ Observation of Germinal Center Cell Apoptosis During a Secondary Immune Response |
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