The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression
Abstract Rel and RelA, individually dispensable for lymphopoiesis, serve unique functions in activated B and T cells. Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mu...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Grossmann, Mathis [verfasserIn] O'Reilly, Lorraine A. [verfasserIn] Gugasyan, Raffi [verfasserIn] Strasser, Andreas [verfasserIn] Adams, Jerry M. [verfasserIn] Gerondakis, Steve [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2000 |
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| Schlagwörter: |
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| Anmerkung: |
© European Molecular Biology Organization 2000 |
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| Übergeordnetes Werk: |
Enthalten in: The EMBO Journal - Nature Publishing Group UK, 2023, 19(2000), 23 vom: 01. Dez., Seite 6351-6360 |
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| Übergeordnetes Werk: |
volume:19 ; year:2000 ; number:23 ; day:01 ; month:12 ; pages:6351-6360 |
| Links: |
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| DOI / URN: |
10.1093/emboj/19.23.6351 |
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| Katalog-ID: |
SPR05800470X |
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| 100 | 1 | |a Grossmann, Mathis |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression |
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| 500 | |a © European Molecular Biology Organization 2000 | ||
| 520 | |a Abstract Rel and RelA, individually dispensable for lymphopoiesis, serve unique functions in activated B and T cells. Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mutant cells lacked mature $ IgM^{lo} $$ IgD^{hi} $ B cells, and numbers of peripheral $ CD4^{+} $ and $ CD8^{+} $ T cells were markedly reduced. The absence of mature B cells was associated with impaired survival that coincided with reduced expression of bcl‐2 and A1. bcl‐2 transgene expression not only prevented apoptosis and increased peripheral B‐cell numbers, but also induced further maturation to an $ IgM^{lo} $$ IgD^{hi} $ phenotype. In contrast, the survival of double‐mutant T cells was normal and the bcl‐2 transgene could not rectify the peripheral T‐cell deficit. These findings indicate that Rel and RelA serve essential, albeit redundant, functions during the later antigen‐independent stages of B‐ and T‐cell maturation, with these transcription factors promoting the survival of peripheral B cells in part by upregulating Bcl‐2. | ||
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| 700 | 1 | |a O'Reilly, Lorraine A. |e verfasserin |4 aut | |
| 700 | 1 | |a Gugasyan, Raffi |e verfasserin |4 aut | |
| 700 | 1 | |a Strasser, Andreas |e verfasserin |4 aut | |
| 700 | 1 | |a Adams, Jerry M. |e verfasserin |4 aut | |
| 700 | 1 | |a Gerondakis, Steve |e verfasserin |4 aut | |
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10.1093/emboj/19.23.6351 doi (DE-627)SPR05800470X (SPR)19.23.6351-e DE-627 ger DE-627 rakwb eng Grossmann, Mathis verfasserin aut The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression 2000 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2000 Abstract Rel and RelA, individually dispensable for lymphopoiesis, serve unique functions in activated B and T cells. Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mutant cells lacked mature $ IgM^{lo} $$ IgD^{hi} $ B cells, and numbers of peripheral $ CD4^{+} $ and $ CD8^{+} $ T cells were markedly reduced. The absence of mature B cells was associated with impaired survival that coincided with reduced expression of bcl‐2 and A1. bcl‐2 transgene expression not only prevented apoptosis and increased peripheral B‐cell numbers, but also induced further maturation to an $ IgM^{lo} $$ IgD^{hi} $ phenotype. In contrast, the survival of double‐mutant T cells was normal and the bcl‐2 transgene could not rectify the peripheral T‐cell deficit. These findings indicate that Rel and RelA serve essential, albeit redundant, functions during the later antigen‐independent stages of B‐ and T‐cell maturation, with these transcription factors promoting the survival of peripheral B cells in part by upregulating Bcl‐2. apoptosis (dpeaa)DE-He213 Bcl‐2 (dpeaa)DE-He213 lymphopoiesis (dpeaa)DE-He213 NF‐κB (dpeaa)DE-He213 transgenics (dpeaa)DE-He213 O'Reilly, Lorraine A. verfasserin aut Gugasyan, Raffi verfasserin aut Strasser, Andreas verfasserin aut Adams, Jerry M. verfasserin aut Gerondakis, Steve verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 19(2000), 23 vom: 01. Dez., Seite 6351-6360 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:19 year:2000 number:23 day:01 month:12 pages:6351-6360 https://dx.doi.org/10.1093/emboj/19.23.6351 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 19 2000 23 01 12 6351-6360 |
| spelling |
10.1093/emboj/19.23.6351 doi (DE-627)SPR05800470X (SPR)19.23.6351-e DE-627 ger DE-627 rakwb eng Grossmann, Mathis verfasserin aut The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression 2000 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2000 Abstract Rel and RelA, individually dispensable for lymphopoiesis, serve unique functions in activated B and T cells. Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mutant cells lacked mature $ IgM^{lo} $$ IgD^{hi} $ B cells, and numbers of peripheral $ CD4^{+} $ and $ CD8^{+} $ T cells were markedly reduced. The absence of mature B cells was associated with impaired survival that coincided with reduced expression of bcl‐2 and A1. bcl‐2 transgene expression not only prevented apoptosis and increased peripheral B‐cell numbers, but also induced further maturation to an $ IgM^{lo} $$ IgD^{hi} $ phenotype. In contrast, the survival of double‐mutant T cells was normal and the bcl‐2 transgene could not rectify the peripheral T‐cell deficit. These findings indicate that Rel and RelA serve essential, albeit redundant, functions during the later antigen‐independent stages of B‐ and T‐cell maturation, with these transcription factors promoting the survival of peripheral B cells in part by upregulating Bcl‐2. apoptosis (dpeaa)DE-He213 Bcl‐2 (dpeaa)DE-He213 lymphopoiesis (dpeaa)DE-He213 NF‐κB (dpeaa)DE-He213 transgenics (dpeaa)DE-He213 O'Reilly, Lorraine A. verfasserin aut Gugasyan, Raffi verfasserin aut Strasser, Andreas verfasserin aut Adams, Jerry M. verfasserin aut Gerondakis, Steve verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 19(2000), 23 vom: 01. Dez., Seite 6351-6360 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:19 year:2000 number:23 day:01 month:12 pages:6351-6360 https://dx.doi.org/10.1093/emboj/19.23.6351 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 19 2000 23 01 12 6351-6360 |
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10.1093/emboj/19.23.6351 doi (DE-627)SPR05800470X (SPR)19.23.6351-e DE-627 ger DE-627 rakwb eng Grossmann, Mathis verfasserin aut The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression 2000 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2000 Abstract Rel and RelA, individually dispensable for lymphopoiesis, serve unique functions in activated B and T cells. Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mutant cells lacked mature $ IgM^{lo} $$ IgD^{hi} $ B cells, and numbers of peripheral $ CD4^{+} $ and $ CD8^{+} $ T cells were markedly reduced. The absence of mature B cells was associated with impaired survival that coincided with reduced expression of bcl‐2 and A1. bcl‐2 transgene expression not only prevented apoptosis and increased peripheral B‐cell numbers, but also induced further maturation to an $ IgM^{lo} $$ IgD^{hi} $ phenotype. In contrast, the survival of double‐mutant T cells was normal and the bcl‐2 transgene could not rectify the peripheral T‐cell deficit. These findings indicate that Rel and RelA serve essential, albeit redundant, functions during the later antigen‐independent stages of B‐ and T‐cell maturation, with these transcription factors promoting the survival of peripheral B cells in part by upregulating Bcl‐2. apoptosis (dpeaa)DE-He213 Bcl‐2 (dpeaa)DE-He213 lymphopoiesis (dpeaa)DE-He213 NF‐κB (dpeaa)DE-He213 transgenics (dpeaa)DE-He213 O'Reilly, Lorraine A. verfasserin aut Gugasyan, Raffi verfasserin aut Strasser, Andreas verfasserin aut Adams, Jerry M. verfasserin aut Gerondakis, Steve verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 19(2000), 23 vom: 01. Dez., Seite 6351-6360 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:19 year:2000 number:23 day:01 month:12 pages:6351-6360 https://dx.doi.org/10.1093/emboj/19.23.6351 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 19 2000 23 01 12 6351-6360 |
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10.1093/emboj/19.23.6351 doi (DE-627)SPR05800470X (SPR)19.23.6351-e DE-627 ger DE-627 rakwb eng Grossmann, Mathis verfasserin aut The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression 2000 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2000 Abstract Rel and RelA, individually dispensable for lymphopoiesis, serve unique functions in activated B and T cells. Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mutant cells lacked mature $ IgM^{lo} $$ IgD^{hi} $ B cells, and numbers of peripheral $ CD4^{+} $ and $ CD8^{+} $ T cells were markedly reduced. The absence of mature B cells was associated with impaired survival that coincided with reduced expression of bcl‐2 and A1. bcl‐2 transgene expression not only prevented apoptosis and increased peripheral B‐cell numbers, but also induced further maturation to an $ IgM^{lo} $$ IgD^{hi} $ phenotype. In contrast, the survival of double‐mutant T cells was normal and the bcl‐2 transgene could not rectify the peripheral T‐cell deficit. These findings indicate that Rel and RelA serve essential, albeit redundant, functions during the later antigen‐independent stages of B‐ and T‐cell maturation, with these transcription factors promoting the survival of peripheral B cells in part by upregulating Bcl‐2. apoptosis (dpeaa)DE-He213 Bcl‐2 (dpeaa)DE-He213 lymphopoiesis (dpeaa)DE-He213 NF‐κB (dpeaa)DE-He213 transgenics (dpeaa)DE-He213 O'Reilly, Lorraine A. verfasserin aut Gugasyan, Raffi verfasserin aut Strasser, Andreas verfasserin aut Adams, Jerry M. verfasserin aut Gerondakis, Steve verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 19(2000), 23 vom: 01. Dez., Seite 6351-6360 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:19 year:2000 number:23 day:01 month:12 pages:6351-6360 https://dx.doi.org/10.1093/emboj/19.23.6351 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 19 2000 23 01 12 6351-6360 |
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10.1093/emboj/19.23.6351 doi (DE-627)SPR05800470X (SPR)19.23.6351-e DE-627 ger DE-627 rakwb eng Grossmann, Mathis verfasserin aut The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression 2000 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 2000 Abstract Rel and RelA, individually dispensable for lymphopoiesis, serve unique functions in activated B and T cells. Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mutant cells lacked mature $ IgM^{lo} $$ IgD^{hi} $ B cells, and numbers of peripheral $ CD4^{+} $ and $ CD8^{+} $ T cells were markedly reduced. The absence of mature B cells was associated with impaired survival that coincided with reduced expression of bcl‐2 and A1. bcl‐2 transgene expression not only prevented apoptosis and increased peripheral B‐cell numbers, but also induced further maturation to an $ IgM^{lo} $$ IgD^{hi} $ phenotype. In contrast, the survival of double‐mutant T cells was normal and the bcl‐2 transgene could not rectify the peripheral T‐cell deficit. These findings indicate that Rel and RelA serve essential, albeit redundant, functions during the later antigen‐independent stages of B‐ and T‐cell maturation, with these transcription factors promoting the survival of peripheral B cells in part by upregulating Bcl‐2. apoptosis (dpeaa)DE-He213 Bcl‐2 (dpeaa)DE-He213 lymphopoiesis (dpeaa)DE-He213 NF‐κB (dpeaa)DE-He213 transgenics (dpeaa)DE-He213 O'Reilly, Lorraine A. verfasserin aut Gugasyan, Raffi verfasserin aut Strasser, Andreas verfasserin aut Adams, Jerry M. verfasserin aut Gerondakis, Steve verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 19(2000), 23 vom: 01. Dez., Seite 6351-6360 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:19 year:2000 number:23 day:01 month:12 pages:6351-6360 https://dx.doi.org/10.1093/emboj/19.23.6351 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 19 2000 23 01 12 6351-6360 |
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Enthalten in The EMBO Journal 19(2000), 23 vom: 01. Dez., Seite 6351-6360 volume:19 year:2000 number:23 day:01 month:12 pages:6351-6360 |
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Grossmann, Mathis @@aut@@ O'Reilly, Lorraine A. @@aut@@ Gugasyan, Raffi @@aut@@ Strasser, Andreas @@aut@@ Adams, Jerry M. @@aut@@ Gerondakis, Steve @@aut@@ |
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Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mutant cells lacked mature $ IgM^{lo} $$ IgD^{hi} $ B cells, and numbers of peripheral $ CD4^{+} $ and $ CD8^{+} $ T cells were markedly reduced. The absence of mature B cells was associated with impaired survival that coincided with reduced expression of bcl‐2 and A1. bcl‐2 transgene expression not only prevented apoptosis and increased peripheral B‐cell numbers, but also induced further maturation to an $ IgM^{lo} $$ IgD^{hi} $ phenotype. In contrast, the survival of double‐mutant T cells was normal and the bcl‐2 transgene could not rectify the peripheral T‐cell deficit. 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Grossmann, Mathis |
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Grossmann, Mathis misc apoptosis misc Bcl‐2 misc lymphopoiesis misc NF‐κB misc transgenics The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression |
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The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression apoptosis (dpeaa)DE-He213 Bcl‐2 (dpeaa)DE-He213 lymphopoiesis (dpeaa)DE-He213 NF‐κB (dpeaa)DE-He213 transgenics (dpeaa)DE-He213 |
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the anti‐apoptotic activities of rel and rela required during b‐cell maturation involve the regulation of bcl‐2 expression |
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The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression |
| abstract |
Abstract Rel and RelA, individually dispensable for lymphopoiesis, serve unique functions in activated B and T cells. Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mutant cells lacked mature $ IgM^{lo} $$ IgD^{hi} $ B cells, and numbers of peripheral $ CD4^{+} $ and $ CD8^{+} $ T cells were markedly reduced. The absence of mature B cells was associated with impaired survival that coincided with reduced expression of bcl‐2 and A1. bcl‐2 transgene expression not only prevented apoptosis and increased peripheral B‐cell numbers, but also induced further maturation to an $ IgM^{lo} $$ IgD^{hi} $ phenotype. In contrast, the survival of double‐mutant T cells was normal and the bcl‐2 transgene could not rectify the peripheral T‐cell deficit. These findings indicate that Rel and RelA serve essential, albeit redundant, functions during the later antigen‐independent stages of B‐ and T‐cell maturation, with these transcription factors promoting the survival of peripheral B cells in part by upregulating Bcl‐2. © European Molecular Biology Organization 2000 |
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Abstract Rel and RelA, individually dispensable for lymphopoiesis, serve unique functions in activated B and T cells. Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mutant cells lacked mature $ IgM^{lo} $$ IgD^{hi} $ B cells, and numbers of peripheral $ CD4^{+} $ and $ CD8^{+} $ T cells were markedly reduced. The absence of mature B cells was associated with impaired survival that coincided with reduced expression of bcl‐2 and A1. bcl‐2 transgene expression not only prevented apoptosis and increased peripheral B‐cell numbers, but also induced further maturation to an $ IgM^{lo} $$ IgD^{hi} $ phenotype. In contrast, the survival of double‐mutant T cells was normal and the bcl‐2 transgene could not rectify the peripheral T‐cell deficit. These findings indicate that Rel and RelA serve essential, albeit redundant, functions during the later antigen‐independent stages of B‐ and T‐cell maturation, with these transcription factors promoting the survival of peripheral B cells in part by upregulating Bcl‐2. © European Molecular Biology Organization 2000 |
| abstract_unstemmed |
Abstract Rel and RelA, individually dispensable for lymphopoiesis, serve unique functions in activated B and T cells. Here their combined roles in lymphocyte development were examined in chimeric mice repopulated with c‐rel−/− rela−/− fetal liver hemopoietic stem cells. Mice engrafted with double‐mutant cells lacked mature $ IgM^{lo} $$ IgD^{hi} $ B cells, and numbers of peripheral $ CD4^{+} $ and $ CD8^{+} $ T cells were markedly reduced. The absence of mature B cells was associated with impaired survival that coincided with reduced expression of bcl‐2 and A1. bcl‐2 transgene expression not only prevented apoptosis and increased peripheral B‐cell numbers, but also induced further maturation to an $ IgM^{lo} $$ IgD^{hi} $ phenotype. In contrast, the survival of double‐mutant T cells was normal and the bcl‐2 transgene could not rectify the peripheral T‐cell deficit. These findings indicate that Rel and RelA serve essential, albeit redundant, functions during the later antigen‐independent stages of B‐ and T‐cell maturation, with these transcription factors promoting the survival of peripheral B cells in part by upregulating Bcl‐2. © European Molecular Biology Organization 2000 |
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The anti‐apoptotic activities of Rel and RelA required during B‐cell maturation involve the regulation of Bcl‐2 expression |
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https://dx.doi.org/10.1093/emboj/19.23.6351 |
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O'Reilly, Lorraine A. Gugasyan, Raffi Strasser, Andreas Adams, Jerry M. Gerondakis, Steve |
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10.1093/emboj/19.23.6351 |
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| score |
7.4002256 |