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Tetraspanin CD9 modulates ADAM17-mediated shedding of LR11 in leukocytes
LR11, also known as SorLA or SORL1, is a type-I membrane protein from which a large extracellular part, soluble LR11 (sLR11), is released by proteolytic shedding on cleavage with a disintegrin and metalloproteinase 17 (ADAM17). A shedding mechanism is presumed to have a key role in the functions of...
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Published in: | Experimental & molecular medicine 2014, 46(0), , pp.1-9 |
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creator | Shokichi Tsukamoto Masahiro Takeuchi Takeharu Kawaguchi Emi Togasaki Atsuko Yamazaki Yasumasa Sugita Tomoya Muto Shio Sakai Yusuke Takeda Chikako Ohwada Emiko Sakaida Naomi Shimizu Keigo Nishii Meizi Jiang Koutaro Yokote Hideaki Bujo Chiaki Nakaseko |
description | LR11, also known as SorLA or SORL1, is a type-I membrane protein from which a large extracellular part, soluble LR11 (sLR11), is released by proteolytic shedding on cleavage with a disintegrin and metalloproteinase 17 (ADAM17). A shedding mechanism is presumed to have a key role in the functions of LR11, but the evidence for this has not yet been demonstrated. Tetraspanin CD9 has been recently shown to regulate the ADAM17-mediated shedding of tumor necrosis factor-a and intercellular adhesion molecule-1 on the cell surface. Here, we investigated the role of CD9 on the shedding of LR11 in leukocytes. LR11 was not expressed in THP-1 monocytes, but it was expressed and released in phorbol 12-myristate13-acetate (PMA)-induced THP-1 macrophages (PMA/THP-1). Confocal microscopy showed colocalization of LR11 and CD9 proteins on the cell surface of PMA/THP-1. Ectopic neo-expression of CD9 in CCRF-SB cells, which are LR11-positive and CD9-negative, reduced the amount of sLR11 released from the cells. In contrast, incubation of LR11-transfected THP-1 cells with neutralizing anti-CD9 monoclonal antibodies increased the amount of sLR11 released from the cells. Likewise, the PMA-stimulated release of sLR11 increased in THP-1 cells transfected with CD9-targeted shRNAs, which was negated by treatment with the metalloproteinase inhibitor GM6001. These results suggest that the tetraspanin CD9 modulates the ADAM17-mediated shedding of LR11 in various leukemia cell lines and that the association between LR11 and CD9 on the cell surface has an important role in the ADAM17-mediated shedding mechanism. KCI Citation Count: 13 |
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fullrecord | <record><control><sourceid>nrf</sourceid><recordid>TN_cdi_nrf_kci_oai_kci_go_kr_ARTI_1088949</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>oai_kci_go_kr_ARTI_1088949</sourcerecordid><originalsourceid>FETCH-nrf_kci_oai_kci_go_kr_ARTI_10889493</originalsourceid><addsrcrecordid>eNqVi7sKwjAAAIMoWB__kNUhkJd9jKVVFHQp3UNo0hrbJtK0g39vEX_A6Ti4W4CA4oSikBO2BAGhNEQsJGwNNt4_MaZHHvEAXEo9DtK_pDUWZnkCe6emTo7awzRP7yRCvVZmdgX9QytlbANdDW8FIXA-Oj21rnrP-Q6satl5vf9xCw7nU5ldkB1q0VZGOGm-bJxoB5EW5VUQHMcJT9g_7QdbLT_q</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Tetraspanin CD9 modulates ADAM17-mediated shedding of LR11 in leukocytes</title><source>Publicly Available Content Database</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Shokichi Tsukamoto ; Masahiro Takeuchi ; Takeharu Kawaguchi ; Emi Togasaki ; Atsuko Yamazaki ; Yasumasa Sugita ; Tomoya Muto ; Shio Sakai ; Yusuke Takeda ; Chikako Ohwada ; Emiko Sakaida ; Naomi Shimizu ; Keigo Nishii ; Meizi Jiang ; Koutaro Yokote ; Hideaki Bujo ; Chiaki Nakaseko</creator><creatorcontrib>Shokichi Tsukamoto ; Masahiro Takeuchi ; Takeharu Kawaguchi ; Emi Togasaki ; Atsuko Yamazaki ; Yasumasa Sugita ; Tomoya Muto ; Shio Sakai ; Yusuke Takeda ; Chikako Ohwada ; Emiko Sakaida ; Naomi Shimizu ; Keigo Nishii ; Meizi Jiang ; Koutaro Yokote ; Hideaki Bujo ; Chiaki Nakaseko</creatorcontrib><description>LR11, also known as SorLA or SORL1, is a type-I membrane protein from which a large extracellular part, soluble LR11 (sLR11), is released by proteolytic shedding on cleavage with a disintegrin and metalloproteinase 17 (ADAM17). A shedding mechanism is presumed to have a key role in the functions of LR11, but the evidence for this has not yet been demonstrated. Tetraspanin CD9 has been recently shown to regulate the ADAM17-mediated shedding of tumor necrosis factor-a and intercellular adhesion molecule-1 on the cell surface. Here, we investigated the role of CD9 on the shedding of LR11 in leukocytes. LR11 was not expressed in THP-1 monocytes, but it was expressed and released in phorbol 12-myristate13-acetate (PMA)-induced THP-1 macrophages (PMA/THP-1). Confocal microscopy showed colocalization of LR11 and CD9 proteins on the cell surface of PMA/THP-1. Ectopic neo-expression of CD9 in CCRF-SB cells, which are LR11-positive and CD9-negative, reduced the amount of sLR11 released from the cells. In contrast, incubation of LR11-transfected THP-1 cells with neutralizing anti-CD9 monoclonal antibodies increased the amount of sLR11 released from the cells. Likewise, the PMA-stimulated release of sLR11 increased in THP-1 cells transfected with CD9-targeted shRNAs, which was negated by treatment with the metalloproteinase inhibitor GM6001. These results suggest that the tetraspanin CD9 modulates the ADAM17-mediated shedding of LR11 in various leukemia cell lines and that the association between LR11 and CD9 on the cell surface has an important role in the ADAM17-mediated shedding mechanism. KCI Citation Count: 13</description><identifier>ISSN: 1226-3613</identifier><identifier>EISSN: 2092-6413</identifier><language>eng</language><publisher>생화학분자생물학회</publisher><subject>생화학</subject><ispartof>Experimental and Molecular Medicine, 2014, 46(0), , pp.1-9</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001870119$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Shokichi Tsukamoto</creatorcontrib><creatorcontrib>Masahiro Takeuchi</creatorcontrib><creatorcontrib>Takeharu Kawaguchi</creatorcontrib><creatorcontrib>Emi Togasaki</creatorcontrib><creatorcontrib>Atsuko Yamazaki</creatorcontrib><creatorcontrib>Yasumasa Sugita</creatorcontrib><creatorcontrib>Tomoya Muto</creatorcontrib><creatorcontrib>Shio Sakai</creatorcontrib><creatorcontrib>Yusuke Takeda</creatorcontrib><creatorcontrib>Chikako Ohwada</creatorcontrib><creatorcontrib>Emiko Sakaida</creatorcontrib><creatorcontrib>Naomi Shimizu</creatorcontrib><creatorcontrib>Keigo Nishii</creatorcontrib><creatorcontrib>Meizi Jiang</creatorcontrib><creatorcontrib>Koutaro Yokote</creatorcontrib><creatorcontrib>Hideaki Bujo</creatorcontrib><creatorcontrib>Chiaki Nakaseko</creatorcontrib><title>Tetraspanin CD9 modulates ADAM17-mediated shedding of LR11 in leukocytes</title><title>Experimental & molecular medicine</title><description>LR11, also known as SorLA or SORL1, is a type-I membrane protein from which a large extracellular part, soluble LR11 (sLR11), is released by proteolytic shedding on cleavage with a disintegrin and metalloproteinase 17 (ADAM17). A shedding mechanism is presumed to have a key role in the functions of LR11, but the evidence for this has not yet been demonstrated. Tetraspanin CD9 has been recently shown to regulate the ADAM17-mediated shedding of tumor necrosis factor-a and intercellular adhesion molecule-1 on the cell surface. Here, we investigated the role of CD9 on the shedding of LR11 in leukocytes. LR11 was not expressed in THP-1 monocytes, but it was expressed and released in phorbol 12-myristate13-acetate (PMA)-induced THP-1 macrophages (PMA/THP-1). Confocal microscopy showed colocalization of LR11 and CD9 proteins on the cell surface of PMA/THP-1. Ectopic neo-expression of CD9 in CCRF-SB cells, which are LR11-positive and CD9-negative, reduced the amount of sLR11 released from the cells. In contrast, incubation of LR11-transfected THP-1 cells with neutralizing anti-CD9 monoclonal antibodies increased the amount of sLR11 released from the cells. Likewise, the PMA-stimulated release of sLR11 increased in THP-1 cells transfected with CD9-targeted shRNAs, which was negated by treatment with the metalloproteinase inhibitor GM6001. These results suggest that the tetraspanin CD9 modulates the ADAM17-mediated shedding of LR11 in various leukemia cell lines and that the association between LR11 and CD9 on the cell surface has an important role in the ADAM17-mediated shedding mechanism. KCI Citation Count: 13</description><subject>생화학</subject><issn>1226-3613</issn><issn>2092-6413</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqVi7sKwjAAAIMoWB__kNUhkJd9jKVVFHQp3UNo0hrbJtK0g39vEX_A6Ti4W4CA4oSikBO2BAGhNEQsJGwNNt4_MaZHHvEAXEo9DtK_pDUWZnkCe6emTo7awzRP7yRCvVZmdgX9QytlbANdDW8FIXA-Oj21rnrP-Q6satl5vf9xCw7nU5ldkB1q0VZGOGm-bJxoB5EW5VUQHMcJT9g_7QdbLT_q</recordid><startdate>201404</startdate><enddate>201404</enddate><creator>Shokichi Tsukamoto</creator><creator>Masahiro Takeuchi</creator><creator>Takeharu Kawaguchi</creator><creator>Emi Togasaki</creator><creator>Atsuko Yamazaki</creator><creator>Yasumasa Sugita</creator><creator>Tomoya Muto</creator><creator>Shio Sakai</creator><creator>Yusuke Takeda</creator><creator>Chikako Ohwada</creator><creator>Emiko Sakaida</creator><creator>Naomi Shimizu</creator><creator>Keigo Nishii</creator><creator>Meizi Jiang</creator><creator>Koutaro Yokote</creator><creator>Hideaki Bujo</creator><creator>Chiaki Nakaseko</creator><general>생화학분자생물학회</general><scope>ACYCR</scope></search><sort><creationdate>201404</creationdate><title>Tetraspanin CD9 modulates ADAM17-mediated shedding of LR11 in leukocytes</title><author>Shokichi Tsukamoto ; Masahiro Takeuchi ; Takeharu Kawaguchi ; Emi Togasaki ; Atsuko Yamazaki ; Yasumasa Sugita ; Tomoya Muto ; Shio Sakai ; Yusuke Takeda ; Chikako Ohwada ; Emiko Sakaida ; Naomi Shimizu ; Keigo Nishii ; Meizi Jiang ; Koutaro Yokote ; Hideaki Bujo ; Chiaki Nakaseko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-nrf_kci_oai_kci_go_kr_ARTI_10889493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>생화학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shokichi Tsukamoto</creatorcontrib><creatorcontrib>Masahiro Takeuchi</creatorcontrib><creatorcontrib>Takeharu Kawaguchi</creatorcontrib><creatorcontrib>Emi Togasaki</creatorcontrib><creatorcontrib>Atsuko Yamazaki</creatorcontrib><creatorcontrib>Yasumasa Sugita</creatorcontrib><creatorcontrib>Tomoya Muto</creatorcontrib><creatorcontrib>Shio Sakai</creatorcontrib><creatorcontrib>Yusuke Takeda</creatorcontrib><creatorcontrib>Chikako Ohwada</creatorcontrib><creatorcontrib>Emiko Sakaida</creatorcontrib><creatorcontrib>Naomi Shimizu</creatorcontrib><creatorcontrib>Keigo Nishii</creatorcontrib><creatorcontrib>Meizi Jiang</creatorcontrib><creatorcontrib>Koutaro Yokote</creatorcontrib><creatorcontrib>Hideaki Bujo</creatorcontrib><creatorcontrib>Chiaki Nakaseko</creatorcontrib><collection>Korean Citation Index</collection><jtitle>Experimental & molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shokichi Tsukamoto</au><au>Masahiro Takeuchi</au><au>Takeharu Kawaguchi</au><au>Emi Togasaki</au><au>Atsuko Yamazaki</au><au>Yasumasa Sugita</au><au>Tomoya Muto</au><au>Shio Sakai</au><au>Yusuke Takeda</au><au>Chikako Ohwada</au><au>Emiko Sakaida</au><au>Naomi Shimizu</au><au>Keigo Nishii</au><au>Meizi Jiang</au><au>Koutaro Yokote</au><au>Hideaki Bujo</au><au>Chiaki Nakaseko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tetraspanin CD9 modulates ADAM17-mediated shedding of LR11 in leukocytes</atitle><jtitle>Experimental & molecular medicine</jtitle><date>2014-04</date><risdate>2014</risdate><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>1226-3613</issn><eissn>2092-6413</eissn><abstract>LR11, also known as SorLA or SORL1, is a type-I membrane protein from which a large extracellular part, soluble LR11 (sLR11), is released by proteolytic shedding on cleavage with a disintegrin and metalloproteinase 17 (ADAM17). A shedding mechanism is presumed to have a key role in the functions of LR11, but the evidence for this has not yet been demonstrated. Tetraspanin CD9 has been recently shown to regulate the ADAM17-mediated shedding of tumor necrosis factor-a and intercellular adhesion molecule-1 on the cell surface. Here, we investigated the role of CD9 on the shedding of LR11 in leukocytes. LR11 was not expressed in THP-1 monocytes, but it was expressed and released in phorbol 12-myristate13-acetate (PMA)-induced THP-1 macrophages (PMA/THP-1). Confocal microscopy showed colocalization of LR11 and CD9 proteins on the cell surface of PMA/THP-1. Ectopic neo-expression of CD9 in CCRF-SB cells, which are LR11-positive and CD9-negative, reduced the amount of sLR11 released from the cells. In contrast, incubation of LR11-transfected THP-1 cells with neutralizing anti-CD9 monoclonal antibodies increased the amount of sLR11 released from the cells. Likewise, the PMA-stimulated release of sLR11 increased in THP-1 cells transfected with CD9-targeted shRNAs, which was negated by treatment with the metalloproteinase inhibitor GM6001. These results suggest that the tetraspanin CD9 modulates the ADAM17-mediated shedding of LR11 in various leukemia cell lines and that the association between LR11 and CD9 on the cell surface has an important role in the ADAM17-mediated shedding mechanism. KCI Citation Count: 13</abstract><pub>생화학분자생물학회</pub></addata></record> |
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subjects | 생화학 |
title | Tetraspanin CD9 modulates ADAM17-mediated shedding of LR11 in leukocytes |
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