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Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans
Clearance of apoptotic cells by engulfment plays an important role in the homeostasis and development of multicellular organisms. Despite the fact that the recognition of apoptotic cells by engulfment receptors is critical in inducing the engulfment process, the molecular mechanisms are still poorly...
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Published in: | PLoS genetics 2012-05, Vol.8 (5), p.e1002663-e1002663 |
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description | Clearance of apoptotic cells by engulfment plays an important role in the homeostasis and development of multicellular organisms. Despite the fact that the recognition of apoptotic cells by engulfment receptors is critical in inducing the engulfment process, the molecular mechanisms are still poorly understood. Here, we characterize a novel cell corpse engulfment pathway mediated by the integrin α subunit PAT-2 in Caenorhabditis elegans and show that it specifically functions in muscle-mediated engulfment during embryogenesis. Inactivation of pat-2 results in a defect in apoptotic cell internalization. The PAT-2 extracellular region binds to the surface of apoptotic cells in vivo, and the intracellular region may mediate signaling for engulfment. We identify essential roles of small GTPase CDC-42 and its activator UIG-1, a guanine-nucleotide exchange factor, in PAT-2-mediated cell corpse removal. PAT-2 and CDC-42 both function in muscle cells for apoptotic cell removal and are co-localized in growing muscle pseudopods around apoptotic cells. Our data suggest that PAT-2 functions through UIG-1 for CDC-42 activation, which in turn leads to cytoskeletal rearrangement and apoptotic cell internalization by muscle cells. Moreover, in contrast to PAT-2, the other integrin α subunit INA-1 and the engulfment receptor CED-1, which signal through the conserved signaling molecules CED-5 (DOCK180)/CED-12 (ELMO) or CED-6 (GULP) respectively, preferentially act in epithelial cells to mediate cell corpse removal during mid-embryogenesis. Our results show that different engulfing cells utilize distinct repertoires of receptors for engulfment at the whole organism level. |
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Despite the fact that the recognition of apoptotic cells by engulfment receptors is critical in inducing the engulfment process, the molecular mechanisms are still poorly understood. Here, we characterize a novel cell corpse engulfment pathway mediated by the integrin α subunit PAT-2 in Caenorhabditis elegans and show that it specifically functions in muscle-mediated engulfment during embryogenesis. Inactivation of pat-2 results in a defect in apoptotic cell internalization. The PAT-2 extracellular region binds to the surface of apoptotic cells in vivo, and the intracellular region may mediate signaling for engulfment. We identify essential roles of small GTPase CDC-42 and its activator UIG-1, a guanine-nucleotide exchange factor, in PAT-2-mediated cell corpse removal. PAT-2 and CDC-42 both function in muscle cells for apoptotic cell removal and are co-localized in growing muscle pseudopods around apoptotic cells. Our data suggest that PAT-2 functions through UIG-1 for CDC-42 activation, which in turn leads to cytoskeletal rearrangement and apoptotic cell internalization by muscle cells. Moreover, in contrast to PAT-2, the other integrin α subunit INA-1 and the engulfment receptor CED-1, which signal through the conserved signaling molecules CED-5 (DOCK180)/CED-12 (ELMO) or CED-6 (GULP) respectively, preferentially act in epithelial cells to mediate cell corpse removal during mid-embryogenesis. Our results show that different engulfing cells utilize distinct repertoires of receptors for engulfment at the whole organism level.</description><identifier>ISSN: 1553-7404</identifier><identifier>ISSN: 1553-7390</identifier><identifier>EISSN: 1553-7404</identifier><identifier>DOI: 10.1371/journal.pgen.1002663</identifier><identifier>PMID: 22615577</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Apoptosis ; Benzeneacetamides - metabolism ; Biology ; Caenorhabditis elegans ; Caenorhabditis elegans - embryology ; Caenorhabditis elegans - genetics ; Caenorhabditis elegans Proteins - genetics ; Caenorhabditis elegans Proteins - metabolism ; Carrier Proteins - metabolism ; Cell Cycle Proteins - genetics ; Cell Cycle Proteins - metabolism ; Cellular signal transduction ; Cytoskeletal Proteins - metabolism ; Cytoskeleton - genetics ; Cytoskeleton - metabolism ; Embryonic Development ; Genetic aspects ; GTP-Binding Proteins - genetics ; GTP-Binding Proteins - metabolism ; Guanine Nucleotide Exchange Factors - metabolism ; Integrins ; Integrins - metabolism ; Membrane Proteins - metabolism ; Muscle, Skeletal - embryology ; Peptides - genetics ; Peptides - metabolism ; Phosphoproteins - metabolism ; Physiological aspects ; Pyridines - metabolism ; Signal Transduction</subject><ispartof>PLoS genetics, 2012-05, Vol.8 (5), p.e1002663-e1002663</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>Hsieh et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c674t-46d3685721af092d86c3a49bbf68db7f90939b8b52b478173350091954c4be6e3</citedby><cites>FETCH-LOGICAL-c674t-46d3685721af092d86c3a49bbf68db7f90939b8b52b478173350091954c4be6e3</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/PMC3355063/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355063/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,36992,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22615577$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Chisholm, Andrew D.</contributor><creatorcontrib>Hsieh, Hsiao-Han</creatorcontrib><creatorcontrib>Hsu, Tsung-Yuan</creatorcontrib><creatorcontrib>Jiang, Hang-Shiang</creatorcontrib><creatorcontrib>Wu, Yi-Chun</creatorcontrib><title>Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans</title><title>PLoS genetics</title><addtitle>PLoS Genet</addtitle><description>Clearance of apoptotic cells by engulfment plays an important role in the homeostasis and development of multicellular organisms. Despite the fact that the recognition of apoptotic cells by engulfment receptors is critical in inducing the engulfment process, the molecular mechanisms are still poorly understood. Here, we characterize a novel cell corpse engulfment pathway mediated by the integrin α subunit PAT-2 in Caenorhabditis elegans and show that it specifically functions in muscle-mediated engulfment during embryogenesis. Inactivation of pat-2 results in a defect in apoptotic cell internalization. The PAT-2 extracellular region binds to the surface of apoptotic cells in vivo, and the intracellular region may mediate signaling for engulfment. We identify essential roles of small GTPase CDC-42 and its activator UIG-1, a guanine-nucleotide exchange factor, in PAT-2-mediated cell corpse removal. PAT-2 and CDC-42 both function in muscle cells for apoptotic cell removal and are co-localized in growing muscle pseudopods around apoptotic cells. Our data suggest that PAT-2 functions through UIG-1 for CDC-42 activation, which in turn leads to cytoskeletal rearrangement and apoptotic cell internalization by muscle cells. Moreover, in contrast to PAT-2, the other integrin α subunit INA-1 and the engulfment receptor CED-1, which signal through the conserved signaling molecules CED-5 (DOCK180)/CED-12 (ELMO) or CED-6 (GULP) respectively, preferentially act in epithelial cells to mediate cell corpse removal during mid-embryogenesis. Our results show that different engulfing cells utilize distinct repertoires of receptors for engulfment at the whole organism level.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Benzeneacetamides - metabolism</subject><subject>Biology</subject><subject>Caenorhabditis elegans</subject><subject>Caenorhabditis elegans - embryology</subject><subject>Caenorhabditis elegans - genetics</subject><subject>Caenorhabditis elegans Proteins - genetics</subject><subject>Caenorhabditis elegans Proteins - metabolism</subject><subject>Carrier Proteins - metabolism</subject><subject>Cell Cycle Proteins - genetics</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cellular signal transduction</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Cytoskeleton - genetics</subject><subject>Cytoskeleton - metabolism</subject><subject>Embryonic Development</subject><subject>Genetic aspects</subject><subject>GTP-Binding Proteins - genetics</subject><subject>GTP-Binding Proteins - metabolism</subject><subject>Guanine Nucleotide Exchange Factors - metabolism</subject><subject>Integrins</subject><subject>Integrins - metabolism</subject><subject>Membrane Proteins - metabolism</subject><subject>Muscle, Skeletal - embryology</subject><subject>Peptides - genetics</subject><subject>Peptides - metabolism</subject><subject>Phosphoproteins - metabolism</subject><subject>Physiological aspects</subject><subject>Pyridines - metabolism</subject><subject>Signal Transduction</subject><issn>1553-7404</issn><issn>1553-7390</issn><issn>1553-7404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNqVk92K1DAUgIso7rr6BiIFQfSis0nz19wsDOPfwOKKrt6GtD3tZOgks0kq7mP5Ij6TGWdcpuCFkos0J9_5OEl6suwpRjNMBD5fu9FbPcy2PdgZRqjknNzLTjFjpBAU0ftH3yfZoxDWCBFWSfEwOylLnvaEOM1ulzZC743Nf_7IP86vi_J88XpR0DIPpk96Y_vchNzDzWg8tHnnfL4ZQzNAsYHW6JhiaaG9tg3krsv11m2ji6bJGxiGkCfzQoN1fqXr1sTkggF6bcPj7EGnhwBPDvNZ9uXtm-vF--Ly6t1yMb8sGi5oLChvCa-YKLHukCzbijdEU1nXHa_aWnQSSSLrqmZlTUWFBSEMIYklow2tgQM5y5Z7b-v0Wm292Wh_q5w26nfA-V5pn-odQDFSpYFrwQBTXZKKty3FlaSI17QUOLku9q7tWKfjN2Cj18NEOt2xZqV6902lqhjiJAleHgTe3YwQotqYsLsobcGNQWGEGeWV5Cyhz_dor1NpxnYuGZsdrualpEQgJHiiZn-h0mhhYxpnoTMpPkl4NUlITITvsddjCGr5-dN_sB_-nb36OmVfHLEr0ENcBTeM0TgbpiDdg413IXjo7q4aI7XrAnXoArXrAnXogpT27PiZ7pL-_PbkF2R-AWY</recordid><startdate>20120501</startdate><enddate>20120501</enddate><creator>Hsieh, Hsiao-Han</creator><creator>Hsu, Tsung-Yuan</creator><creator>Jiang, Hang-Shiang</creator><creator>Wu, Yi-Chun</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20120501</creationdate><title>Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans</title><author>Hsieh, Hsiao-Han ; Hsu, Tsung-Yuan ; Jiang, Hang-Shiang ; Wu, Yi-Chun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c674t-46d3685721af092d86c3a49bbf68db7f90939b8b52b478173350091954c4be6e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Benzeneacetamides - metabolism</topic><topic>Biology</topic><topic>Caenorhabditis elegans</topic><topic>Caenorhabditis elegans - embryology</topic><topic>Caenorhabditis elegans - genetics</topic><topic>Caenorhabditis elegans Proteins - genetics</topic><topic>Caenorhabditis elegans Proteins - metabolism</topic><topic>Carrier Proteins - metabolism</topic><topic>Cell Cycle Proteins - genetics</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cellular signal transduction</topic><topic>Cytoskeletal Proteins - metabolism</topic><topic>Cytoskeleton - genetics</topic><topic>Cytoskeleton - metabolism</topic><topic>Embryonic Development</topic><topic>Genetic aspects</topic><topic>GTP-Binding Proteins - genetics</topic><topic>GTP-Binding Proteins - metabolism</topic><topic>Guanine Nucleotide Exchange Factors - metabolism</topic><topic>Integrins</topic><topic>Integrins - metabolism</topic><topic>Membrane Proteins - metabolism</topic><topic>Muscle, Skeletal - embryology</topic><topic>Peptides - genetics</topic><topic>Peptides - metabolism</topic><topic>Phosphoproteins - metabolism</topic><topic>Physiological aspects</topic><topic>Pyridines - metabolism</topic><topic>Signal Transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hsieh, Hsiao-Han</creatorcontrib><creatorcontrib>Hsu, Tsung-Yuan</creatorcontrib><creatorcontrib>Jiang, Hang-Shiang</creatorcontrib><creatorcontrib>Wu, Yi-Chun</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>Science in Context</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hsieh, Hsiao-Han</au><au>Hsu, Tsung-Yuan</au><au>Jiang, Hang-Shiang</au><au>Wu, Yi-Chun</au><au>Chisholm, Andrew D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans</atitle><jtitle>PLoS genetics</jtitle><addtitle>PLoS Genet</addtitle><date>2012-05-01</date><risdate>2012</risdate><volume>8</volume><issue>5</issue><spage>e1002663</spage><epage>e1002663</epage><pages>e1002663-e1002663</pages><issn>1553-7404</issn><issn>1553-7390</issn><eissn>1553-7404</eissn><abstract>Clearance of apoptotic cells by engulfment plays an important role in the homeostasis and development of multicellular organisms. Despite the fact that the recognition of apoptotic cells by engulfment receptors is critical in inducing the engulfment process, the molecular mechanisms are still poorly understood. Here, we characterize a novel cell corpse engulfment pathway mediated by the integrin α subunit PAT-2 in Caenorhabditis elegans and show that it specifically functions in muscle-mediated engulfment during embryogenesis. Inactivation of pat-2 results in a defect in apoptotic cell internalization. The PAT-2 extracellular region binds to the surface of apoptotic cells in vivo, and the intracellular region may mediate signaling for engulfment. We identify essential roles of small GTPase CDC-42 and its activator UIG-1, a guanine-nucleotide exchange factor, in PAT-2-mediated cell corpse removal. PAT-2 and CDC-42 both function in muscle cells for apoptotic cell removal and are co-localized in growing muscle pseudopods around apoptotic cells. Our data suggest that PAT-2 functions through UIG-1 for CDC-42 activation, which in turn leads to cytoskeletal rearrangement and apoptotic cell internalization by muscle cells. Moreover, in contrast to PAT-2, the other integrin α subunit INA-1 and the engulfment receptor CED-1, which signal through the conserved signaling molecules CED-5 (DOCK180)/CED-12 (ELMO) or CED-6 (GULP) respectively, preferentially act in epithelial cells to mediate cell corpse removal during mid-embryogenesis. Our results show that different engulfing cells utilize distinct repertoires of receptors for engulfment at the whole organism level.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22615577</pmid><doi>10.1371/journal.pgen.1002663</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis Benzeneacetamides - metabolism Biology Caenorhabditis elegans Caenorhabditis elegans - embryology Caenorhabditis elegans - genetics Caenorhabditis elegans Proteins - genetics Caenorhabditis elegans Proteins - metabolism Carrier Proteins - metabolism Cell Cycle Proteins - genetics Cell Cycle Proteins - metabolism Cellular signal transduction Cytoskeletal Proteins - metabolism Cytoskeleton - genetics Cytoskeleton - metabolism Embryonic Development Genetic aspects GTP-Binding Proteins - genetics GTP-Binding Proteins - metabolism Guanine Nucleotide Exchange Factors - metabolism Integrins Integrins - metabolism Membrane Proteins - metabolism Muscle, Skeletal - embryology Peptides - genetics Peptides - metabolism Phosphoproteins - metabolism Physiological aspects Pyridines - metabolism Signal Transduction |
title | Integrin α PAT-2/CDC-42 signaling is required for muscle-mediated clearance of apoptotic cells in Caenorhabditis elegans |
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