Stat5 expression is critical for mast cell development and survival
Interleukin-3 (IL-3) and stem cell factor (SCF) are important mast cell growth and differentiation factors. Since both cytokines activate the transcription factor signal transducer and activator of transcription 5 (Stat5), a known regulator of proliferation and survival, we investigated the effects...
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Veröffentlicht in: | Blood 2003-08, Vol.102 (4), p.1290-1297 |
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creator | Shelburne, Christopher P. McCoy, Margaret E. Piekorz, Roland Sexl, Veronica Roh, Kwan-Ho Jacobs-Helber, Sarah M. Gillespie, Sheila R. Bailey, Daniel P. Mirmonsef, Paria Mann, Meredith N. Kashyap, Mohit Wright, Harry V. Chong, Hey Jin Bouton, L. Andrew Barnstein, Brian Ramirez, Carlos D. Bunting, Kevin D. Sawyer, Steven Lantz, Chris S. Ryan, John J. |
description | Interleukin-3 (IL-3) and stem cell factor (SCF) are important mast cell growth and differentiation factors. Since both cytokines activate the transcription factor signal transducer and activator of transcription 5 (Stat5), a known regulator of proliferation and survival, we investigated the effects of Stat5 deficiency on mast cell development and survival. Bone marrow–derived mast cell (BMMC) populations cultured from Stat5A/B-deficient mice survived in IL-3 + SCF, but not in either cytokine alone. These cells demonstrated reduced expression of Bcl-2, Bcl-x(L), cyclin A2, and cyclin B1, with increased apoptosis and delayed cell cycle progression during IL-3 or SCF culture. Finally, the absence of Stat5 resulted in loss of in vivo mast cell development, as judged by assessments of Stat5-deficient mice and transplantation of Stat5-deficient bone marrow cells to mast cell-deficient recipient mice. These results indicate that Stat5A and Stat5B are critical regulators of in vitro and in vivo mast cell development and survival. |
doi_str_mv | 10.1182/blood-2002-11-3490 |
format | Article |
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Andrew ; Barnstein, Brian ; Ramirez, Carlos D. ; Bunting, Kevin D. ; Sawyer, Steven ; Lantz, Chris S. ; Ryan, John J.</creator><creatorcontrib>Shelburne, Christopher P. ; McCoy, Margaret E. ; Piekorz, Roland ; Sexl, Veronica ; Roh, Kwan-Ho ; Jacobs-Helber, Sarah M. ; Gillespie, Sheila R. ; Bailey, Daniel P. ; Mirmonsef, Paria ; Mann, Meredith N. ; Kashyap, Mohit ; Wright, Harry V. ; Chong, Hey Jin ; Bouton, L. Andrew ; Barnstein, Brian ; Ramirez, Carlos D. ; Bunting, Kevin D. ; Sawyer, Steven ; Lantz, Chris S. ; Ryan, John J.</creatorcontrib><description>Interleukin-3 (IL-3) and stem cell factor (SCF) are important mast cell growth and differentiation factors. Since both cytokines activate the transcription factor signal transducer and activator of transcription 5 (Stat5), a known regulator of proliferation and survival, we investigated the effects of Stat5 deficiency on mast cell development and survival. Bone marrow–derived mast cell (BMMC) populations cultured from Stat5A/B-deficient mice survived in IL-3 + SCF, but not in either cytokine alone. These cells demonstrated reduced expression of Bcl-2, Bcl-x(L), cyclin A2, and cyclin B1, with increased apoptosis and delayed cell cycle progression during IL-3 or SCF culture. Finally, the absence of Stat5 resulted in loss of in vivo mast cell development, as judged by assessments of Stat5-deficient mice and transplantation of Stat5-deficient bone marrow cells to mast cell-deficient recipient mice. These results indicate that Stat5A and Stat5B are critical regulators of in vitro and in vivo mast cell development and survival.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2002-11-3490</identifier><identifier>PMID: 12714518</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Allergic diseases ; Animals ; Biological and medical sciences ; Caspases - metabolism ; Cells, Cultured ; Cyclins - biosynthesis ; Cyclins - genetics ; DNA-Binding Proteins - biosynthesis ; DNA-Binding Proteins - deficiency ; DNA-Binding Proteins - physiology ; Enzyme Activation - genetics ; General aspects ; Humans ; Immunopathology ; Interleukin-3 - pharmacology ; Mast Cells - cytology ; Mast Cells - physiology ; Medical sciences ; Mice ; Mice, Inbred C57BL ; Milk Proteins ; Mitochondria - physiology ; Proto-Oncogene Proteins c-bcl-2 - biosynthesis ; Recombinant Proteins - pharmacology ; Signal Transduction - drug effects ; Signal Transduction - physiology ; STAT5 Transcription Factor ; Stem Cell Factor - pharmacology ; Trans-Activators - biosynthesis ; Trans-Activators - deficiency ; Trans-Activators - physiology ; Tumor Suppressor Proteins ; Up-Regulation</subject><ispartof>Blood, 2003-08, Vol.102 (4), p.1290-1297</ispartof><rights>2003 American Society of Hematology</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c492t-5dcea94ec592831ddb63c643ef850045bf7a091347c82dffdfafce079a1f06823</citedby><cites>FETCH-LOGICAL-c492t-5dcea94ec592831ddb63c643ef850045bf7a091347c82dffdfafce079a1f06823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15049483$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12714518$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shelburne, Christopher P.</creatorcontrib><creatorcontrib>McCoy, Margaret E.</creatorcontrib><creatorcontrib>Piekorz, Roland</creatorcontrib><creatorcontrib>Sexl, Veronica</creatorcontrib><creatorcontrib>Roh, Kwan-Ho</creatorcontrib><creatorcontrib>Jacobs-Helber, Sarah M.</creatorcontrib><creatorcontrib>Gillespie, Sheila R.</creatorcontrib><creatorcontrib>Bailey, Daniel P.</creatorcontrib><creatorcontrib>Mirmonsef, Paria</creatorcontrib><creatorcontrib>Mann, Meredith N.</creatorcontrib><creatorcontrib>Kashyap, Mohit</creatorcontrib><creatorcontrib>Wright, Harry V.</creatorcontrib><creatorcontrib>Chong, Hey Jin</creatorcontrib><creatorcontrib>Bouton, L. 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These cells demonstrated reduced expression of Bcl-2, Bcl-x(L), cyclin A2, and cyclin B1, with increased apoptosis and delayed cell cycle progression during IL-3 or SCF culture. Finally, the absence of Stat5 resulted in loss of in vivo mast cell development, as judged by assessments of Stat5-deficient mice and transplantation of Stat5-deficient bone marrow cells to mast cell-deficient recipient mice. These results indicate that Stat5A and Stat5B are critical regulators of in vitro and in vivo mast cell development and survival.</description><subject>Allergic diseases</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Caspases - metabolism</subject><subject>Cells, Cultured</subject><subject>Cyclins - biosynthesis</subject><subject>Cyclins - genetics</subject><subject>DNA-Binding Proteins - biosynthesis</subject><subject>DNA-Binding Proteins - deficiency</subject><subject>DNA-Binding Proteins - physiology</subject><subject>Enzyme Activation - genetics</subject><subject>General aspects</subject><subject>Humans</subject><subject>Immunopathology</subject><subject>Interleukin-3 - pharmacology</subject><subject>Mast Cells - cytology</subject><subject>Mast Cells - physiology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Milk Proteins</subject><subject>Mitochondria - physiology</subject><subject>Proto-Oncogene Proteins c-bcl-2 - biosynthesis</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Signal Transduction - drug effects</subject><subject>Signal Transduction - physiology</subject><subject>STAT5 Transcription Factor</subject><subject>Stem Cell Factor - pharmacology</subject><subject>Trans-Activators - biosynthesis</subject><subject>Trans-Activators - deficiency</subject><subject>Trans-Activators - physiology</subject><subject>Tumor Suppressor Proteins</subject><subject>Up-Regulation</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LAzEQhoMoWqt_wIPkorfVyVd3F7xI8QsKHtRzSJMJRHY3NdkW_ffu2kJvnoYZnpl5eQi5YHDDWMVvl02MruAAvGCsELKGAzJhilfFMIJDMgGAWSHrkp2Q05w_AZgUXB2TE8ZLJhWrJmT-1pteUfxeJcw5xI6GTG0KfbCmoT4m2prcU4tNQx1usImrFruems7RvE6bsDHNGTnypsl4vqtT8vH48D5_LhavTy_z-0VhZc37QjmLppZoVc0rwZxbzoSdSYG-UgBSLX1poGZClrbiznvnjbcIZW2Yh1nFxZRcb--uUvxaY-51G_KYzHQY11mXQilecjGAfAvaFHNO6PUqhdakH81Aj-r0nzo9qht6Paobli5319fLFt1-ZedqAK52gMmDHJ9MZ0PecwpkLavx-92Ww8HFJmDS2QbsLLqQ0PbaxfBfjl9NDoxu</recordid><startdate>20030815</startdate><enddate>20030815</enddate><creator>Shelburne, Christopher P.</creator><creator>McCoy, Margaret E.</creator><creator>Piekorz, Roland</creator><creator>Sexl, Veronica</creator><creator>Roh, Kwan-Ho</creator><creator>Jacobs-Helber, Sarah M.</creator><creator>Gillespie, Sheila R.</creator><creator>Bailey, Daniel P.</creator><creator>Mirmonsef, Paria</creator><creator>Mann, Meredith N.</creator><creator>Kashyap, Mohit</creator><creator>Wright, Harry V.</creator><creator>Chong, Hey Jin</creator><creator>Bouton, L. 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Andrew</au><au>Barnstein, Brian</au><au>Ramirez, Carlos D.</au><au>Bunting, Kevin D.</au><au>Sawyer, Steven</au><au>Lantz, Chris S.</au><au>Ryan, John J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stat5 expression is critical for mast cell development and survival</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2003-08-15</date><risdate>2003</risdate><volume>102</volume><issue>4</issue><spage>1290</spage><epage>1297</epage><pages>1290-1297</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Interleukin-3 (IL-3) and stem cell factor (SCF) are important mast cell growth and differentiation factors. Since both cytokines activate the transcription factor signal transducer and activator of transcription 5 (Stat5), a known regulator of proliferation and survival, we investigated the effects of Stat5 deficiency on mast cell development and survival. Bone marrow–derived mast cell (BMMC) populations cultured from Stat5A/B-deficient mice survived in IL-3 + SCF, but not in either cytokine alone. These cells demonstrated reduced expression of Bcl-2, Bcl-x(L), cyclin A2, and cyclin B1, with increased apoptosis and delayed cell cycle progression during IL-3 or SCF culture. Finally, the absence of Stat5 resulted in loss of in vivo mast cell development, as judged by assessments of Stat5-deficient mice and transplantation of Stat5-deficient bone marrow cells to mast cell-deficient recipient mice. These results indicate that Stat5A and Stat5B are critical regulators of in vitro and in vivo mast cell development and survival.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>12714518</pmid><doi>10.1182/blood-2002-11-3490</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Allergic diseases Animals Biological and medical sciences Caspases - metabolism Cells, Cultured Cyclins - biosynthesis Cyclins - genetics DNA-Binding Proteins - biosynthesis DNA-Binding Proteins - deficiency DNA-Binding Proteins - physiology Enzyme Activation - genetics General aspects Humans Immunopathology Interleukin-3 - pharmacology Mast Cells - cytology Mast Cells - physiology Medical sciences Mice Mice, Inbred C57BL Milk Proteins Mitochondria - physiology Proto-Oncogene Proteins c-bcl-2 - biosynthesis Recombinant Proteins - pharmacology Signal Transduction - drug effects Signal Transduction - physiology STAT5 Transcription Factor Stem Cell Factor - pharmacology Trans-Activators - biosynthesis Trans-Activators - deficiency Trans-Activators - physiology Tumor Suppressor Proteins Up-Regulation |
title | Stat5 expression is critical for mast cell development and survival |
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