Pretaporter, a Drosophila protein serving as a ligand for Draper in the phagocytosis of apoptotic cells
Phagocytic removal of cells undergoing apoptosis is necessary for animal development and tissue homeostasis. Draper, a homologue of the Caenorhabditis elegans phagocytosis receptor CED‐1, is responsible for the phagocytosis of apoptotic cells in Drosophila , but its ligand presumably present on apop...
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creator | Kuraishi, Takayuki Nakagawa, Yukiko Nagaosa, Kaz Hashimoto, Yumi Ishimoto, Takashi Moki, Takeshi Fujita, Yu Nakayama, Hiroshi Dohmae, Naoshi Shiratsuchi, Akiko Yamamoto, Naoko Ueda, Koichi Yamaguchi, Masamitsu Awasaki, Takeshi Nakanishi, Yoshinobu |
description | Phagocytic removal of cells undergoing apoptosis is necessary for animal development and tissue homeostasis. Draper, a homologue of the
Caenorhabditis elegans
phagocytosis receptor CED‐1, is responsible for the phagocytosis of apoptotic cells in
Drosophila
, but its ligand presumably present on apoptotic cells remains unknown. An endoplasmic reticulum protein that binds to the extracellular region of Draper was isolated. Loss of this protein, which we name Pretaporter, led to a reduced level of apoptotic cell clearance in embryos, and the overexpression of
pretaporter
in the mutant flies rescued this defect. Results from genetic analyses suggested that Pretaporter functionally interacts with Draper and the corresponding signal mediators. Pretaporter was exposed at the cell surface after the induction of apoptosis, and cells artificially expressing Pretaporter at their surface became susceptible to Draper‐mediated phagocytosis. Finally, the incubation with Pretaporter augmented the tyrosine‐phosphorylation of Draper in phagocytic cells. These results collectively suggest that Pretaporter relocates from the endoplasmic reticulum to the cell surface during apoptosis to serve as a ligand for Draper in the phagocytosis of apoptotic cells. |
doi_str_mv | 10.1038/emboj.2009.343 |
format | Article |
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Caenorhabditis elegans
phagocytosis receptor CED‐1, is responsible for the phagocytosis of apoptotic cells in
Drosophila
, but its ligand presumably present on apoptotic cells remains unknown. An endoplasmic reticulum protein that binds to the extracellular region of Draper was isolated. Loss of this protein, which we name Pretaporter, led to a reduced level of apoptotic cell clearance in embryos, and the overexpression of
pretaporter
in the mutant flies rescued this defect. Results from genetic analyses suggested that Pretaporter functionally interacts with Draper and the corresponding signal mediators. Pretaporter was exposed at the cell surface after the induction of apoptosis, and cells artificially expressing Pretaporter at their surface became susceptible to Draper‐mediated phagocytosis. Finally, the incubation with Pretaporter augmented the tyrosine‐phosphorylation of Draper in phagocytic cells. These results collectively suggest that Pretaporter relocates from the endoplasmic reticulum to the cell surface during apoptosis to serve as a ligand for Draper in the phagocytosis of apoptotic cells.</description><identifier>ISSN: 0261-4189</identifier><identifier>ISSN: 1460-2075</identifier><identifier>EISSN: 1460-2075</identifier><identifier>DOI: 10.1038/emboj.2009.343</identifier><identifier>PMID: 19927123</identifier><identifier>CODEN: EMJODG</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Animals ; Apoptosis ; Caenorhabditis elegans ; Cell Membrane - metabolism ; Developmental biology ; Drosophila ; Drosophila melanogaster - genetics ; Drosophila melanogaster - metabolism ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Drosophila Proteins - physiology ; EMBO07 ; Embryos ; endoplasmic reticulum ; Endoplasmic Reticulum - metabolism ; Gene expression ; Hemocytes - metabolism ; Insects ; Ligands ; Membrane Proteins - genetics ; Membrane Proteins - physiology ; Microscopy, Fluorescence - methods ; Models, Genetic ; Molecular biology ; Mutation ; Phagocytes - metabolism ; Phagocytosis ; Protein Structure, Tertiary ; Proteins ; Signal transduction</subject><ispartof>The EMBO journal, 2009-12, Vol.28 (24), p.3868-3878</ispartof><rights>European Molecular Biology Organization 2009</rights><rights>Copyright © 2009 European Molecular Biology Organization</rights><rights>Copyright Nature Publishing Group Dec 16, 2009</rights><rights>Copyright © 2009, European Molecular Biology Organization 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c7123-4e595d71e305f7b54d55ce2be18bbdec0caf54f4a4ee2aaffeeddef8724d6b833</citedby><cites>FETCH-LOGICAL-c7123-4e595d71e305f7b54d55ce2be18bbdec0caf54f4a4ee2aaffeeddef8724d6b833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797060/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797060/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,1411,1427,27903,27904,41099,42168,45553,45554,46388,46812,51555,53770,53772</link.rule.ids><linktorsrc>$$Uhttps://doi.org/10.1038/emboj.2009.343$$EView_record_in_Springer_Nature$$FView_record_in_$$GSpringer_Nature</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19927123$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuraishi, Takayuki</creatorcontrib><creatorcontrib>Nakagawa, Yukiko</creatorcontrib><creatorcontrib>Nagaosa, Kaz</creatorcontrib><creatorcontrib>Hashimoto, Yumi</creatorcontrib><creatorcontrib>Ishimoto, Takashi</creatorcontrib><creatorcontrib>Moki, Takeshi</creatorcontrib><creatorcontrib>Fujita, Yu</creatorcontrib><creatorcontrib>Nakayama, Hiroshi</creatorcontrib><creatorcontrib>Dohmae, Naoshi</creatorcontrib><creatorcontrib>Shiratsuchi, Akiko</creatorcontrib><creatorcontrib>Yamamoto, Naoko</creatorcontrib><creatorcontrib>Ueda, Koichi</creatorcontrib><creatorcontrib>Yamaguchi, Masamitsu</creatorcontrib><creatorcontrib>Awasaki, Takeshi</creatorcontrib><creatorcontrib>Nakanishi, Yoshinobu</creatorcontrib><title>Pretaporter, a Drosophila protein serving as a ligand for Draper in the phagocytosis of apoptotic cells</title><title>The EMBO journal</title><addtitle>EMBO J</addtitle><addtitle>EMBO J</addtitle><description>Phagocytic removal of cells undergoing apoptosis is necessary for animal development and tissue homeostasis. Draper, a homologue of the
Caenorhabditis elegans
phagocytosis receptor CED‐1, is responsible for the phagocytosis of apoptotic cells in
Drosophila
, but its ligand presumably present on apoptotic cells remains unknown. An endoplasmic reticulum protein that binds to the extracellular region of Draper was isolated. Loss of this protein, which we name Pretaporter, led to a reduced level of apoptotic cell clearance in embryos, and the overexpression of
pretaporter
in the mutant flies rescued this defect. Results from genetic analyses suggested that Pretaporter functionally interacts with Draper and the corresponding signal mediators. Pretaporter was exposed at the cell surface after the induction of apoptosis, and cells artificially expressing Pretaporter at their surface became susceptible to Draper‐mediated phagocytosis. Finally, the incubation with Pretaporter augmented the tyrosine‐phosphorylation of Draper in phagocytic cells. These results collectively suggest that Pretaporter relocates from the endoplasmic reticulum to the cell surface during apoptosis to serve as a ligand for Draper in the phagocytosis of apoptotic cells.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Caenorhabditis elegans</subject><subject>Cell Membrane - metabolism</subject><subject>Developmental biology</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - metabolism</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Drosophila Proteins - physiology</subject><subject>EMBO07</subject><subject>Embryos</subject><subject>endoplasmic reticulum</subject><subject>Endoplasmic Reticulum - metabolism</subject><subject>Gene expression</subject><subject>Hemocytes - metabolism</subject><subject>Insects</subject><subject>Ligands</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - physiology</subject><subject>Microscopy, Fluorescence - methods</subject><subject>Models, Genetic</subject><subject>Molecular biology</subject><subject>Mutation</subject><subject>Phagocytes - metabolism</subject><subject>Phagocytosis</subject><subject>Protein Structure, Tertiary</subject><subject>Proteins</subject><subject>Signal 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a Drosophila protein serving as a ligand for Draper in the phagocytosis of apoptotic cells</title><author>Kuraishi, Takayuki ; Nakagawa, Yukiko ; Nagaosa, Kaz ; Hashimoto, Yumi ; Ishimoto, Takashi ; Moki, Takeshi ; Fujita, Yu ; Nakayama, Hiroshi ; Dohmae, Naoshi ; Shiratsuchi, Akiko ; Yamamoto, Naoko ; Ueda, Koichi ; Yamaguchi, Masamitsu ; Awasaki, Takeshi ; Nakanishi, Yoshinobu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c7123-4e595d71e305f7b54d55ce2be18bbdec0caf54f4a4ee2aaffeeddef8724d6b833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Caenorhabditis elegans</topic><topic>Cell Membrane - metabolism</topic><topic>Developmental biology</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - metabolism</topic><topic>Drosophila Proteins - 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J</addtitle><date>2009-12-16</date><risdate>2009</risdate><volume>28</volume><issue>24</issue><spage>3868</spage><epage>3878</epage><pages>3868-3878</pages><issn>0261-4189</issn><issn>1460-2075</issn><eissn>1460-2075</eissn><coden>EMJODG</coden><abstract>Phagocytic removal of cells undergoing apoptosis is necessary for animal development and tissue homeostasis. Draper, a homologue of the
Caenorhabditis elegans
phagocytosis receptor CED‐1, is responsible for the phagocytosis of apoptotic cells in
Drosophila
, but its ligand presumably present on apoptotic cells remains unknown. An endoplasmic reticulum protein that binds to the extracellular region of Draper was isolated. Loss of this protein, which we name Pretaporter, led to a reduced level of apoptotic cell clearance in embryos, and the overexpression of
pretaporter
in the mutant flies rescued this defect. Results from genetic analyses suggested that Pretaporter functionally interacts with Draper and the corresponding signal mediators. Pretaporter was exposed at the cell surface after the induction of apoptosis, and cells artificially expressing Pretaporter at their surface became susceptible to Draper‐mediated phagocytosis. Finally, the incubation with Pretaporter augmented the tyrosine‐phosphorylation of Draper in phagocytic cells. These results collectively suggest that Pretaporter relocates from the endoplasmic reticulum to the cell surface during apoptosis to serve as a ligand for Draper in the phagocytosis of apoptotic cells.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>19927123</pmid><doi>10.1038/emboj.2009.343</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis Caenorhabditis elegans Cell Membrane - metabolism Developmental biology Drosophila Drosophila melanogaster - genetics Drosophila melanogaster - metabolism Drosophila Proteins - genetics Drosophila Proteins - metabolism Drosophila Proteins - physiology EMBO07 Embryos endoplasmic reticulum Endoplasmic Reticulum - metabolism Gene expression Hemocytes - metabolism Insects Ligands Membrane Proteins - genetics Membrane Proteins - physiology Microscopy, Fluorescence - methods Models, Genetic Molecular biology Mutation Phagocytes - metabolism Phagocytosis Protein Structure, Tertiary Proteins Signal transduction |
title | Pretaporter, a Drosophila protein serving as a ligand for Draper in the phagocytosis of apoptotic cells |
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