Interleukin-12p40 variant form reduces Interleukin-12p80 secretion
•An IL-12p40 variant form was discovered.•The Il12b variant is expressed in activated BMDCs and some lymphoid tissues.•The IL-12p40 variant form suppresses the formation and secretion of IL-12p80. IL-12 is a key cytokine for the promotion of CD4+ T cells differentiation to type 1 helper T cells. IL-...
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Veröffentlicht in: | Cytokine (Philadelphia, Pa.) Pa.), 2019-08, Vol.120, p.251-257 |
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creator | Oshikiri, Yumi Nara, Hidetoshi Takeda, Yuji Araki, Akemi Nemoto, Nobuhito Gazi, Md. Yeashin Saito, Shoko Saitoh, Shinichi Nakajima, Osamu Asao, Hironobu |
description | •An IL-12p40 variant form was discovered.•The Il12b variant is expressed in activated BMDCs and some lymphoid tissues.•The IL-12p40 variant form suppresses the formation and secretion of IL-12p80.
IL-12 is a key cytokine for the promotion of CD4+ T cells differentiation to type 1 helper T cells. IL-12 is a heterodimer (IL-12p70) consisting of p40 and p35 subunits, and is mainly secreted from activated antigen-presenting cells, such as macrophages and dendritic cells (DCs). In this study, we found that activated mouse bone marrow-derived DCs (BMDCs) produced a p40 splice variant form mRNA in addition to the conventional p40 mRNA. This p40 variant mRNA was produced by alternative splicing in exon 5, and possessed a premature stop codon. As a result, the p40 variant protein contained 157 amino acids of the N-terminal part of p40 and an additional 10 novel amino acids. When the p40 variant was expressed in HEK-293T cells, it was not secreted from the cells. To investigate the function of the p40 variant, it was co-expressed with p40 and/or p35. The p40 variant did not affect the secretion of IL-12p40 or IL-12p70, or the function of the secreted p70. In contrast, the secretion of IL-12p80, a homodimeric IL-12 with two p40 subunits, was significantly decreased when the p40 variant was expressed. This new splicing variant p40 may act to fine-tune the function of IL-12p80. |
doi_str_mv | 10.1016/j.cyto.2019.05.017 |
format | Article |
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IL-12 is a key cytokine for the promotion of CD4+ T cells differentiation to type 1 helper T cells. IL-12 is a heterodimer (IL-12p70) consisting of p40 and p35 subunits, and is mainly secreted from activated antigen-presenting cells, such as macrophages and dendritic cells (DCs). In this study, we found that activated mouse bone marrow-derived DCs (BMDCs) produced a p40 splice variant form mRNA in addition to the conventional p40 mRNA. This p40 variant mRNA was produced by alternative splicing in exon 5, and possessed a premature stop codon. As a result, the p40 variant protein contained 157 amino acids of the N-terminal part of p40 and an additional 10 novel amino acids. When the p40 variant was expressed in HEK-293T cells, it was not secreted from the cells. To investigate the function of the p40 variant, it was co-expressed with p40 and/or p35. The p40 variant did not affect the secretion of IL-12p40 or IL-12p70, or the function of the secreted p70. In contrast, the secretion of IL-12p80, a homodimeric IL-12 with two p40 subunits, was significantly decreased when the p40 variant was expressed. This new splicing variant p40 may act to fine-tune the function of IL-12p80.</description><identifier>ISSN: 1043-4666</identifier><identifier>EISSN: 1096-0023</identifier><identifier>DOI: 10.1016/j.cyto.2019.05.017</identifier><identifier>PMID: 31146247</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>IL-12p40 ; IL-12p80 ; Interleukin-12 ; Splice variant</subject><ispartof>Cytokine (Philadelphia, Pa.), 2019-08, Vol.120, p.251-257</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-a5943ecc94a4e7849544ef2f60f247136194786384c43c2a322347f213aca523</citedby><cites>FETCH-LOGICAL-c356t-a5943ecc94a4e7849544ef2f60f247136194786384c43c2a322347f213aca523</cites><orcidid>0000-0001-9352-2446 ; 0000-0002-0823-1802</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cyto.2019.05.017$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31146247$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oshikiri, Yumi</creatorcontrib><creatorcontrib>Nara, Hidetoshi</creatorcontrib><creatorcontrib>Takeda, Yuji</creatorcontrib><creatorcontrib>Araki, Akemi</creatorcontrib><creatorcontrib>Nemoto, Nobuhito</creatorcontrib><creatorcontrib>Gazi, Md. Yeashin</creatorcontrib><creatorcontrib>Saito, Shoko</creatorcontrib><creatorcontrib>Saitoh, Shinichi</creatorcontrib><creatorcontrib>Nakajima, Osamu</creatorcontrib><creatorcontrib>Asao, Hironobu</creatorcontrib><title>Interleukin-12p40 variant form reduces Interleukin-12p80 secretion</title><title>Cytokine (Philadelphia, Pa.)</title><addtitle>Cytokine</addtitle><description>•An IL-12p40 variant form was discovered.•The Il12b variant is expressed in activated BMDCs and some lymphoid tissues.•The IL-12p40 variant form suppresses the formation and secretion of IL-12p80.
IL-12 is a key cytokine for the promotion of CD4+ T cells differentiation to type 1 helper T cells. IL-12 is a heterodimer (IL-12p70) consisting of p40 and p35 subunits, and is mainly secreted from activated antigen-presenting cells, such as macrophages and dendritic cells (DCs). In this study, we found that activated mouse bone marrow-derived DCs (BMDCs) produced a p40 splice variant form mRNA in addition to the conventional p40 mRNA. This p40 variant mRNA was produced by alternative splicing in exon 5, and possessed a premature stop codon. As a result, the p40 variant protein contained 157 amino acids of the N-terminal part of p40 and an additional 10 novel amino acids. When the p40 variant was expressed in HEK-293T cells, it was not secreted from the cells. To investigate the function of the p40 variant, it was co-expressed with p40 and/or p35. The p40 variant did not affect the secretion of IL-12p40 or IL-12p70, or the function of the secreted p70. In contrast, the secretion of IL-12p80, a homodimeric IL-12 with two p40 subunits, was significantly decreased when the p40 variant was expressed. This new splicing variant p40 may act to fine-tune the function of IL-12p80.</description><subject>IL-12p40</subject><subject>IL-12p80</subject><subject>Interleukin-12</subject><subject>Splice variant</subject><issn>1043-4666</issn><issn>1096-0023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kD1PwzAQhi0EolD4AwwoI0vC2b44icQCFR-VKrF0t4xzkVzyUeykUv89iVoYGJjuhud9dfcwdsMh4cDV_Sax-75LBPAigTQBnp2wCw6FigGEPJ12lDEqpWbsMoQNABQyy87ZTHKOSmB2wZ6WbU--puHTtTEXW4RoZ7wzbR9VnW8iT-VgKUR_sByiQNZT77r2ip1Vpg50fZxztn55Xi_e4tX763LxuIqtTFUfm7RASdYWaJCyHIsUkSpRKajGS7hUvMAsVzJHi9IKI4WQmFWCS2NNKuSc3R1qt777Gij0unHBUl2blroh6BGXeYoK1YiKA2p9F4KnSm-9a4zfaw56Uqc3elKnJ3UaUj2qG0O3x_7ho6HyN_LjagQeDgCNT-4ceR2so9ZS6TzZXped-6__G56MfUc</recordid><startdate>201908</startdate><enddate>201908</enddate><creator>Oshikiri, Yumi</creator><creator>Nara, Hidetoshi</creator><creator>Takeda, Yuji</creator><creator>Araki, Akemi</creator><creator>Nemoto, Nobuhito</creator><creator>Gazi, Md. Yeashin</creator><creator>Saito, Shoko</creator><creator>Saitoh, Shinichi</creator><creator>Nakajima, Osamu</creator><creator>Asao, Hironobu</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9352-2446</orcidid><orcidid>https://orcid.org/0000-0002-0823-1802</orcidid></search><sort><creationdate>201908</creationdate><title>Interleukin-12p40 variant form reduces Interleukin-12p80 secretion</title><author>Oshikiri, Yumi ; Nara, Hidetoshi ; Takeda, Yuji ; Araki, Akemi ; Nemoto, Nobuhito ; Gazi, Md. Yeashin ; Saito, Shoko ; Saitoh, Shinichi ; Nakajima, Osamu ; Asao, Hironobu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-a5943ecc94a4e7849544ef2f60f247136194786384c43c2a322347f213aca523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>IL-12p40</topic><topic>IL-12p80</topic><topic>Interleukin-12</topic><topic>Splice variant</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oshikiri, Yumi</creatorcontrib><creatorcontrib>Nara, Hidetoshi</creatorcontrib><creatorcontrib>Takeda, Yuji</creatorcontrib><creatorcontrib>Araki, Akemi</creatorcontrib><creatorcontrib>Nemoto, Nobuhito</creatorcontrib><creatorcontrib>Gazi, Md. Yeashin</creatorcontrib><creatorcontrib>Saito, Shoko</creatorcontrib><creatorcontrib>Saitoh, Shinichi</creatorcontrib><creatorcontrib>Nakajima, Osamu</creatorcontrib><creatorcontrib>Asao, Hironobu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cytokine (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oshikiri, Yumi</au><au>Nara, Hidetoshi</au><au>Takeda, Yuji</au><au>Araki, Akemi</au><au>Nemoto, Nobuhito</au><au>Gazi, Md. Yeashin</au><au>Saito, Shoko</au><au>Saitoh, Shinichi</au><au>Nakajima, Osamu</au><au>Asao, Hironobu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interleukin-12p40 variant form reduces Interleukin-12p80 secretion</atitle><jtitle>Cytokine (Philadelphia, Pa.)</jtitle><addtitle>Cytokine</addtitle><date>2019-08</date><risdate>2019</risdate><volume>120</volume><spage>251</spage><epage>257</epage><pages>251-257</pages><issn>1043-4666</issn><eissn>1096-0023</eissn><abstract>•An IL-12p40 variant form was discovered.•The Il12b variant is expressed in activated BMDCs and some lymphoid tissues.•The IL-12p40 variant form suppresses the formation and secretion of IL-12p80.
IL-12 is a key cytokine for the promotion of CD4+ T cells differentiation to type 1 helper T cells. IL-12 is a heterodimer (IL-12p70) consisting of p40 and p35 subunits, and is mainly secreted from activated antigen-presenting cells, such as macrophages and dendritic cells (DCs). In this study, we found that activated mouse bone marrow-derived DCs (BMDCs) produced a p40 splice variant form mRNA in addition to the conventional p40 mRNA. This p40 variant mRNA was produced by alternative splicing in exon 5, and possessed a premature stop codon. As a result, the p40 variant protein contained 157 amino acids of the N-terminal part of p40 and an additional 10 novel amino acids. When the p40 variant was expressed in HEK-293T cells, it was not secreted from the cells. To investigate the function of the p40 variant, it was co-expressed with p40 and/or p35. The p40 variant did not affect the secretion of IL-12p40 or IL-12p70, or the function of the secreted p70. In contrast, the secretion of IL-12p80, a homodimeric IL-12 with two p40 subunits, was significantly decreased when the p40 variant was expressed. This new splicing variant p40 may act to fine-tune the function of IL-12p80.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>31146247</pmid><doi>10.1016/j.cyto.2019.05.017</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-9352-2446</orcidid><orcidid>https://orcid.org/0000-0002-0823-1802</orcidid></addata></record> |
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subjects | IL-12p40 IL-12p80 Interleukin-12 Splice variant |
title | Interleukin-12p40 variant form reduces Interleukin-12p80 secretion |
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