Induction of globin mRNA expression by interleukin-3 in a stem cell factor-dependent SV-40 T-antigen-immortalized multipotent hematopoietic cell line
Erythropoiesis requires the stepwise action on immature progenitors of several growth factors, including stem cell factor (SCF), interleukin 3 (IL‐3), and erythropoietin (Epo). Epo is required to sustain proliferation and survival of committed progenitors and might further modulate the level of expr...
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Veröffentlicht in: | Journal of cellular physiology 2003-04, Vol.195 (1), p.38-49 |
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creator | Cairns, Linda Cirò, Marco Minuzzo, Mario Morlé, François Starck, Joëlle Ottolenghi, Sergio Ronchi, Antonella |
description | Erythropoiesis requires the stepwise action on immature progenitors of several growth factors, including stem cell factor (SCF), interleukin 3 (IL‐3), and erythropoietin (Epo). Epo is required to sustain proliferation and survival of committed progenitors and might further modulate the level of expression of several erythroid genes, including globin genes. Here we report a new SCF‐dependent immortalized mouse progenitor cell line (GATA‐1 ts SCF) that can also grow in either Epo or IL‐3 as the sole growth factor. When grown in SCF, these cells show an “open” chromatin structure of the β‐globin LCR, but do not significantly express globin. However, Epo or IL‐3 induce globin expression and are required for its maintainance. This effect of IL‐3 is unexpected as IL‐3 was previously reported either to be unable to induce hemoglobinization, or even to antagonize it. This suggests that GATA‐1 ts SCF cells may have progressed to a stage in which globin genes are already poised for expression and only require signal(s) that can be elicited by either Epo or IL‐3. Through the use of inhibitors, we suggest that p38 may be one of the molecules modulating induction and maintenance of globin expression. © 2003 Wiley‐Liss, Inc. |
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Epo is required to sustain proliferation and survival of committed progenitors and might further modulate the level of expression of several erythroid genes, including globin genes. Here we report a new SCF‐dependent immortalized mouse progenitor cell line (GATA‐1 ts SCF) that can also grow in either Epo or IL‐3 as the sole growth factor. When grown in SCF, these cells show an “open” chromatin structure of the β‐globin LCR, but do not significantly express globin. However, Epo or IL‐3 induce globin expression and are required for its maintainance. This effect of IL‐3 is unexpected as IL‐3 was previously reported either to be unable to induce hemoglobinization, or even to antagonize it. This suggests that GATA‐1 ts SCF cells may have progressed to a stage in which globin genes are already poised for expression and only require signal(s) that can be elicited by either Epo or IL‐3. Through the use of inhibitors, we suggest that p38 may be one of the molecules modulating induction and maintenance of globin expression. © 2003 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.10241</identifier><identifier>PMID: 12599207</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Antigens, Differentiation - biosynthesis ; Antigens, Polyomavirus Transforming ; Cell Line, Transformed ; Enzyme Inhibitors - pharmacology ; Erythropoietin - pharmacology ; Gene Expression Regulation - drug effects ; Globins - biosynthesis ; Globins - genetics ; Hematopoietic Stem Cells - cytology ; Hematopoietic Stem Cells - drug effects ; Hematopoietic Stem Cells - metabolism ; Hemoglobins - biosynthesis ; Interleukin-3 - pharmacology ; Mice ; Mitogen-Activated Protein Kinases - antagonists & inhibitors ; Mitogen-Activated Protein Kinases - metabolism ; Multipotent Stem Cells - cytology ; Multipotent Stem Cells - drug effects ; Multipotent Stem Cells - metabolism ; p38 Mitogen-Activated Protein Kinases ; RNA, Messenger - biosynthesis ; Signal Transduction - drug effects ; Stem Cell Factor - pharmacology</subject><ispartof>Journal of cellular physiology, 2003-04, Vol.195 (1), p.38-49</ispartof><rights>Copyright © 2003 Wiley‐Liss, Inc.</rights><rights>Copyright 2003 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3591-c50d701c5c8df66d81e19de158474a3ebabbcab4d38155c60530dd94ad13999d3</citedby><cites>FETCH-LOGICAL-c3591-c50d701c5c8df66d81e19de158474a3ebabbcab4d38155c60530dd94ad13999d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcp.10241$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcp.10241$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12599207$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cairns, Linda</creatorcontrib><creatorcontrib>Cirò, Marco</creatorcontrib><creatorcontrib>Minuzzo, Mario</creatorcontrib><creatorcontrib>Morlé, François</creatorcontrib><creatorcontrib>Starck, Joëlle</creatorcontrib><creatorcontrib>Ottolenghi, Sergio</creatorcontrib><creatorcontrib>Ronchi, Antonella</creatorcontrib><title>Induction of globin mRNA expression by interleukin-3 in a stem cell factor-dependent SV-40 T-antigen-immortalized multipotent hematopoietic cell line</title><title>Journal of cellular physiology</title><addtitle>J. Cell. Physiol</addtitle><description>Erythropoiesis requires the stepwise action on immature progenitors of several growth factors, including stem cell factor (SCF), interleukin 3 (IL‐3), and erythropoietin (Epo). Epo is required to sustain proliferation and survival of committed progenitors and might further modulate the level of expression of several erythroid genes, including globin genes. Here we report a new SCF‐dependent immortalized mouse progenitor cell line (GATA‐1 ts SCF) that can also grow in either Epo or IL‐3 as the sole growth factor. When grown in SCF, these cells show an “open” chromatin structure of the β‐globin LCR, but do not significantly express globin. However, Epo or IL‐3 induce globin expression and are required for its maintainance. This effect of IL‐3 is unexpected as IL‐3 was previously reported either to be unable to induce hemoglobinization, or even to antagonize it. This suggests that GATA‐1 ts SCF cells may have progressed to a stage in which globin genes are already poised for expression and only require signal(s) that can be elicited by either Epo or IL‐3. Through the use of inhibitors, we suggest that p38 may be one of the molecules modulating induction and maintenance of globin expression. © 2003 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Antigens, Differentiation - biosynthesis</subject><subject>Antigens, Polyomavirus Transforming</subject><subject>Cell Line, Transformed</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Erythropoietin - pharmacology</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Globins - biosynthesis</subject><subject>Globins - genetics</subject><subject>Hematopoietic Stem Cells - cytology</subject><subject>Hematopoietic Stem Cells - drug effects</subject><subject>Hematopoietic Stem Cells - metabolism</subject><subject>Hemoglobins - biosynthesis</subject><subject>Interleukin-3 - pharmacology</subject><subject>Mice</subject><subject>Mitogen-Activated Protein Kinases - antagonists & inhibitors</subject><subject>Mitogen-Activated Protein Kinases - metabolism</subject><subject>Multipotent Stem Cells - cytology</subject><subject>Multipotent Stem Cells - drug effects</subject><subject>Multipotent Stem Cells - metabolism</subject><subject>p38 Mitogen-Activated Protein Kinases</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Signal Transduction - drug effects</subject><subject>Stem Cell Factor - pharmacology</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1O3DAURi3UCqaURV-g8rYLFzuOk_GSDjDlR4BaSpeWY99Qg2NHjkdl-h59XzIN0BWre6--c7_FQegDo58ZpcX-nenHpSjZFpoxKmtSVqJ4g2ZjxogUJdtB74bhjlIqJefbaIcVQsqC1jP09yTYlckuBhxbfOtj4wLuvl0cYHjoEwzDJmnW2IUMycPq3gXCxwtrPGTosAHvcatNjolY6CFYCBl_vyElxddEh-xuIRDXdTFl7d0fsLhb-ez6mDfgL-h0jn10kJ2ZyrwL8B69bbUfYO9p7qIfx0fXi6_k_HJ5sjg4J4YLyYgR1NaUGWHmtq0qO2fApAUm5mVdag6Nbhqjm9LyORPCVFRwaq0stWVcSmn5Lvo09ZoUhyFBq_rkOp3WilG1UatGteqf2pH9OLH9qunA_iefXI7A_gT8dh7Wrzep08XVcyWZPtzo8uHlQ6d7VdW8FurnxVIdnn2RS351pjh_BKkylHQ</recordid><startdate>200304</startdate><enddate>200304</enddate><creator>Cairns, Linda</creator><creator>Cirò, Marco</creator><creator>Minuzzo, Mario</creator><creator>Morlé, François</creator><creator>Starck, Joëlle</creator><creator>Ottolenghi, Sergio</creator><creator>Ronchi, Antonella</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200304</creationdate><title>Induction of globin mRNA expression by interleukin-3 in a stem cell factor-dependent SV-40 T-antigen-immortalized multipotent hematopoietic cell line</title><author>Cairns, Linda ; Cirò, Marco ; Minuzzo, Mario ; Morlé, François ; Starck, Joëlle ; Ottolenghi, Sergio ; Ronchi, Antonella</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3591-c50d701c5c8df66d81e19de158474a3ebabbcab4d38155c60530dd94ad13999d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Antigens, Differentiation - biosynthesis</topic><topic>Antigens, Polyomavirus Transforming</topic><topic>Cell Line, Transformed</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Erythropoietin - pharmacology</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Globins - biosynthesis</topic><topic>Globins - genetics</topic><topic>Hematopoietic Stem Cells - cytology</topic><topic>Hematopoietic Stem Cells - drug effects</topic><topic>Hematopoietic Stem Cells - metabolism</topic><topic>Hemoglobins - biosynthesis</topic><topic>Interleukin-3 - pharmacology</topic><topic>Mice</topic><topic>Mitogen-Activated Protein Kinases - antagonists & inhibitors</topic><topic>Mitogen-Activated Protein Kinases - metabolism</topic><topic>Multipotent Stem Cells - cytology</topic><topic>Multipotent Stem Cells - drug effects</topic><topic>Multipotent Stem Cells - metabolism</topic><topic>p38 Mitogen-Activated Protein Kinases</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Signal Transduction - drug effects</topic><topic>Stem Cell Factor - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cairns, Linda</creatorcontrib><creatorcontrib>Cirò, Marco</creatorcontrib><creatorcontrib>Minuzzo, Mario</creatorcontrib><creatorcontrib>Morlé, François</creatorcontrib><creatorcontrib>Starck, Joëlle</creatorcontrib><creatorcontrib>Ottolenghi, Sergio</creatorcontrib><creatorcontrib>Ronchi, Antonella</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cairns, Linda</au><au>Cirò, Marco</au><au>Minuzzo, Mario</au><au>Morlé, François</au><au>Starck, Joëlle</au><au>Ottolenghi, Sergio</au><au>Ronchi, Antonella</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of globin mRNA expression by interleukin-3 in a stem cell factor-dependent SV-40 T-antigen-immortalized multipotent hematopoietic cell line</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J. Cell. Physiol</addtitle><date>2003-04</date><risdate>2003</risdate><volume>195</volume><issue>1</issue><spage>38</spage><epage>49</epage><pages>38-49</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>Erythropoiesis requires the stepwise action on immature progenitors of several growth factors, including stem cell factor (SCF), interleukin 3 (IL‐3), and erythropoietin (Epo). Epo is required to sustain proliferation and survival of committed progenitors and might further modulate the level of expression of several erythroid genes, including globin genes. Here we report a new SCF‐dependent immortalized mouse progenitor cell line (GATA‐1 ts SCF) that can also grow in either Epo or IL‐3 as the sole growth factor. When grown in SCF, these cells show an “open” chromatin structure of the β‐globin LCR, but do not significantly express globin. However, Epo or IL‐3 induce globin expression and are required for its maintainance. This effect of IL‐3 is unexpected as IL‐3 was previously reported either to be unable to induce hemoglobinization, or even to antagonize it. This suggests that GATA‐1 ts SCF cells may have progressed to a stage in which globin genes are already poised for expression and only require signal(s) that can be elicited by either Epo or IL‐3. Through the use of inhibitors, we suggest that p38 may be one of the molecules modulating induction and maintenance of globin expression. © 2003 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12599207</pmid><doi>10.1002/jcp.10241</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Antigens, Differentiation - biosynthesis Antigens, Polyomavirus Transforming Cell Line, Transformed Enzyme Inhibitors - pharmacology Erythropoietin - pharmacology Gene Expression Regulation - drug effects Globins - biosynthesis Globins - genetics Hematopoietic Stem Cells - cytology Hematopoietic Stem Cells - drug effects Hematopoietic Stem Cells - metabolism Hemoglobins - biosynthesis Interleukin-3 - pharmacology Mice Mitogen-Activated Protein Kinases - antagonists & inhibitors Mitogen-Activated Protein Kinases - metabolism Multipotent Stem Cells - cytology Multipotent Stem Cells - drug effects Multipotent Stem Cells - metabolism p38 Mitogen-Activated Protein Kinases RNA, Messenger - biosynthesis Signal Transduction - drug effects Stem Cell Factor - pharmacology |
title | Induction of globin mRNA expression by interleukin-3 in a stem cell factor-dependent SV-40 T-antigen-immortalized multipotent hematopoietic cell line |
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