The special unfolded protein response in plasma cells
The high rate of antibody production places considerable metabolic and folding stress on plasma cells (PC). Not surprisingly, they rely on the unfolded protein response (UPR), a universal signaling, and transcriptional network that monitors the health of the secretory pathway and mounts cellular res...
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Veröffentlicht in: | Immunological reviews 2021-09, Vol.303 (1), p.35-51 |
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description | The high rate of antibody production places considerable metabolic and folding stress on plasma cells (PC). Not surprisingly, they rely on the unfolded protein response (UPR), a universal signaling, and transcriptional network that monitors the health of the secretory pathway and mounts cellular responses to stress. Typically, the UPR utilizes three distinct stress sensors in the ER membrane, each regulating a subset of targets to re‐establish homeostasis. PC use a specialized UPR scheme—they preemptively trigger the UPR via developmental signals and suppress two of the sensors, PERK and ATF6, relying on IRE1 alone. The specialized PC UPR program is tuned to the specific needs at every stage of development—from early biogenesis of secretory apparatus, to massive immunoglobulin expression later. Furthermore, the UPR in PC integrates with other pathways essential in a highly secretory cell—mTOR pathway that ensures efficient synthesis, autophagosomes that recycle components of the synthetic machinery, and apoptotic signaling that controls cell fate in the face of excessive folding stress. This specialized PC program is not shared with other secretory cells, for reasons yet to be defined. In this review, we give a perspective into how and why PC need such a unique UPR program. |
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Not surprisingly, they rely on the unfolded protein response (UPR), a universal signaling, and transcriptional network that monitors the health of the secretory pathway and mounts cellular responses to stress. Typically, the UPR utilizes three distinct stress sensors in the ER membrane, each regulating a subset of targets to re‐establish homeostasis. PC use a specialized UPR scheme—they preemptively trigger the UPR via developmental signals and suppress two of the sensors, PERK and ATF6, relying on IRE1 alone. The specialized PC UPR program is tuned to the specific needs at every stage of development—from early biogenesis of secretory apparatus, to massive immunoglobulin expression later. Furthermore, the UPR in PC integrates with other pathways essential in a highly secretory cell—mTOR pathway that ensures efficient synthesis, autophagosomes that recycle components of the synthetic machinery, and apoptotic signaling that controls cell fate in the face of excessive folding stress. This specialized PC program is not shared with other secretory cells, for reasons yet to be defined. In this review, we give a perspective into how and why PC need such a unique UPR program.</description><identifier>ISSN: 0105-2896</identifier><identifier>EISSN: 1600-065X</identifier><identifier>DOI: 10.1111/imr.13012</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Antibodies ; anticipatory unfolded protein response ; Apoptosis ; autophagy ; Cell fate ; Developmental stages ; expansion of secretory apparatus ; Folding ; Homeostasis ; inactivation of sensors ; Phagosomes ; Plasma cells ; Protein folding ; Proteins ; Sensors ; Signal transduction ; Signaling ; TOR protein ; Transcription</subject><ispartof>Immunological reviews, 2021-09, Vol.303 (1), p.35-51</ispartof><rights>2021 John Wiley & Sons A/S. 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This specialized PC program is not shared with other secretory cells, for reasons yet to be defined. In this review, we give a perspective into how and why PC need such a unique UPR program.</description><subject>Antibodies</subject><subject>anticipatory unfolded protein response</subject><subject>Apoptosis</subject><subject>autophagy</subject><subject>Cell fate</subject><subject>Developmental stages</subject><subject>expansion of secretory apparatus</subject><subject>Folding</subject><subject>Homeostasis</subject><subject>inactivation of sensors</subject><subject>Phagosomes</subject><subject>Plasma cells</subject><subject>Protein folding</subject><subject>Proteins</subject><subject>Sensors</subject><subject>Signal transduction</subject><subject>Signaling</subject><subject>TOR protein</subject><subject>Transcription</subject><issn>0105-2896</issn><issn>1600-065X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LxDAQhoMouK4e_AcFTx66O5O0aXuUxY-FFUFW8BbSZoJdsm1Ntsj-e6P16lxmDs_MvDyMXSMsMNay3fsFCkB-wmYoAVKQ-fspmwFCnvKykufsIoQdABaCZzOWbz8oCQM1rXbJ2NneGTLJ4PsDtV3iKQx9FyiJ8-B02OukIefCJTuz2gW6-utz9vZwv109pZuXx_XqbpM2QgBPs4qXyDmIqiQ0UpumNIVpbF2CKAvUNsuKvNZUaIuEmbRQE6eYODOAIq_FnN1Md2Ogz5HCQe360XfxpeK5FFLmkleRup2oxvcheLJq8O1e-6NCUD9WVLSifq1EdjmxX62j4_-gWj-_ThvfOORiRA</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Ricci, Daniela</creator><creator>Gidalevitz, Tali</creator><creator>Argon, Yair</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T5</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>M7N</scope><orcidid>https://orcid.org/0000-0001-6156-3825</orcidid></search><sort><creationdate>202109</creationdate><title>The special unfolded protein response in plasma cells</title><author>Ricci, Daniela ; Gidalevitz, Tali ; Argon, Yair</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3302-49281220398e1d6adc8d7dcfb803871af4475bae7af1e146f0be2e0654d0135b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antibodies</topic><topic>anticipatory unfolded protein response</topic><topic>Apoptosis</topic><topic>autophagy</topic><topic>Cell fate</topic><topic>Developmental stages</topic><topic>expansion of secretory apparatus</topic><topic>Folding</topic><topic>Homeostasis</topic><topic>inactivation of sensors</topic><topic>Phagosomes</topic><topic>Plasma cells</topic><topic>Protein folding</topic><topic>Proteins</topic><topic>Sensors</topic><topic>Signal transduction</topic><topic>Signaling</topic><topic>TOR protein</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ricci, Daniela</creatorcontrib><creatorcontrib>Gidalevitz, Tali</creatorcontrib><creatorcontrib>Argon, Yair</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Immunological reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ricci, Daniela</au><au>Gidalevitz, Tali</au><au>Argon, Yair</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The special unfolded protein response in plasma cells</atitle><jtitle>Immunological reviews</jtitle><date>2021-09</date><risdate>2021</risdate><volume>303</volume><issue>1</issue><spage>35</spage><epage>51</epage><pages>35-51</pages><issn>0105-2896</issn><eissn>1600-065X</eissn><abstract>The high rate of antibody production places considerable metabolic and folding stress on plasma cells (PC). Not surprisingly, they rely on the unfolded protein response (UPR), a universal signaling, and transcriptional network that monitors the health of the secretory pathway and mounts cellular responses to stress. Typically, the UPR utilizes three distinct stress sensors in the ER membrane, each regulating a subset of targets to re‐establish homeostasis. PC use a specialized UPR scheme—they preemptively trigger the UPR via developmental signals and suppress two of the sensors, PERK and ATF6, relying on IRE1 alone. The specialized PC UPR program is tuned to the specific needs at every stage of development—from early biogenesis of secretory apparatus, to massive immunoglobulin expression later. Furthermore, the UPR in PC integrates with other pathways essential in a highly secretory cell—mTOR pathway that ensures efficient synthesis, autophagosomes that recycle components of the synthetic machinery, and apoptotic signaling that controls cell fate in the face of excessive folding stress. 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subjects | Antibodies anticipatory unfolded protein response Apoptosis autophagy Cell fate Developmental stages expansion of secretory apparatus Folding Homeostasis inactivation of sensors Phagosomes Plasma cells Protein folding Proteins Sensors Signal transduction Signaling TOR protein Transcription |
title | The special unfolded protein response in plasma cells |
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