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Regulation of bone mass and osteoclast function depend on the F-actin modulator SWAP-70
Bone remodeling involves tightly regulated bone‐resorbing osteoclasts and bone‐forming osteoblasts. Determining osteoclast function is central to understanding bone diseases such as osteoporosis and osteopetrosis. Here, we report a novel function of the F‐actin binding and regulatory protein SWAP‐70...
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Published in: | Journal of bone and mineral research 2012-10, Vol.27 (10), p.2085-2096 |
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container_title | Journal of bone and mineral research |
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creator | Garbe, Annette I Roscher, Anne Schüler, Christiane Lutter, Anne-Helen Glösmann, Martin Bernhardt, Ricardo Chopin, Michael Hempel, Ute Hofbauer, Lorenz C Rammelt, Stefan Egerbacher, Monika Erben, Reinhold G Jessberger, Rolf |
description | Bone remodeling involves tightly regulated bone‐resorbing osteoclasts and bone‐forming osteoblasts. Determining osteoclast function is central to understanding bone diseases such as osteoporosis and osteopetrosis. Here, we report a novel function of the F‐actin binding and regulatory protein SWAP‐70 in osteoclast biology. F‐actin ring formation, cell morphology, and bone resorption are impaired in Swap‐70−/− osteoclasts, whereas the expression of osteoclast differentiation markers induced in vitro by macrophage colony‐stimulating factor (M‐CSF) and receptor activator of NF‐κB ligand (RANKL) remains unaffected. Swap‐70−/− mice develop osteopetrosis with increased bone mass, abnormally dense bone, and impaired osteoclast function. Ectopic expression of SWAP‐70 in Swap‐70−/− osteoclasts in vitro rescues their deficiencies in bone resorption and F‐actin ring formation. Rescue requires a functional pleckstrin homology (PH) domain, known to support membrane localization of SWAP‐70, and the F‐actin binding domain. Transplantation of SWAP‐70–proficient bone marrow into Swap‐70−/− mice restores osteoclast resorption capacity in vivo. The identification of the role of SWAP‐70 in promoting osteoclast function through modulating membrane‐proximal F‐actin rearrangements reveals a new pathway to control osteoclasts and bone homeostasis. © 2012 American Society for Bone and Mineral Research. |
doi_str_mv | 10.1002/jbmr.1670 |
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Determining osteoclast function is central to understanding bone diseases such as osteoporosis and osteopetrosis. Here, we report a novel function of the F‐actin binding and regulatory protein SWAP‐70 in osteoclast biology. F‐actin ring formation, cell morphology, and bone resorption are impaired in Swap‐70−/− osteoclasts, whereas the expression of osteoclast differentiation markers induced in vitro by macrophage colony‐stimulating factor (M‐CSF) and receptor activator of NF‐κB ligand (RANKL) remains unaffected. Swap‐70−/− mice develop osteopetrosis with increased bone mass, abnormally dense bone, and impaired osteoclast function. Ectopic expression of SWAP‐70 in Swap‐70−/− osteoclasts in vitro rescues their deficiencies in bone resorption and F‐actin ring formation. Rescue requires a functional pleckstrin homology (PH) domain, known to support membrane localization of SWAP‐70, and the F‐actin binding domain. Transplantation of SWAP‐70–proficient bone marrow into Swap‐70−/− mice restores osteoclast resorption capacity in vivo. The identification of the role of SWAP‐70 in promoting osteoclast function through modulating membrane‐proximal F‐actin rearrangements reveals a new pathway to control osteoclasts and bone homeostasis. © 2012 American Society for Bone and Mineral Research.</description><identifier>ISSN: 0884-0431</identifier><identifier>EISSN: 1523-4681</identifier><identifier>DOI: 10.1002/jbmr.1670</identifier><identifier>PMID: 22648978</identifier><identifier>CODEN: JBMREJ</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Actins - metabolism ; Animals ; Biological and medical sciences ; BONE ; Bone and Bones - pathology ; Bone Resorption - complications ; Bone Resorption - pathology ; Cell Line ; Cell Movement ; DNA-Binding Proteins - deficiency ; DNA-Binding Proteins - metabolism ; F-ACTIN ; Fundamental and applied biological sciences. Psychology ; Guanine Nucleotide Exchange Factors - deficiency ; Guanine Nucleotide Exchange Factors - metabolism ; Humans ; Indexing in process ; Mice ; Minor Histocompatibility Antigens ; Nuclear Proteins - deficiency ; Nuclear Proteins - metabolism ; Organ Size ; Osteoblasts - pathology ; OSTEOCLASTS ; Osteoclasts - metabolism ; Osteoclasts - pathology ; Osteopetrosis - complications ; Osteopetrosis - pathology ; RESORPTION ; Skeleton and joints ; SWAP-70 ; Vertebrates: osteoarticular system, musculoskeletal system</subject><ispartof>Journal of bone and mineral research, 2012-10, Vol.27 (10), p.2085-2096</ispartof><rights>Copyright © 2012 American Society for Bone and Mineral Research</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 American Society for Bone and Mineral Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5550-3efa15e6fd25ab9ddc38175c9f294cc5ec968fc3db527d7a3c48cd6b61596f763</citedby><cites>FETCH-LOGICAL-c5550-3efa15e6fd25ab9ddc38175c9f294cc5ec968fc3db527d7a3c48cd6b61596f763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26351539$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22648978$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garbe, Annette I</creatorcontrib><creatorcontrib>Roscher, Anne</creatorcontrib><creatorcontrib>Schüler, Christiane</creatorcontrib><creatorcontrib>Lutter, Anne-Helen</creatorcontrib><creatorcontrib>Glösmann, Martin</creatorcontrib><creatorcontrib>Bernhardt, Ricardo</creatorcontrib><creatorcontrib>Chopin, Michael</creatorcontrib><creatorcontrib>Hempel, Ute</creatorcontrib><creatorcontrib>Hofbauer, Lorenz C</creatorcontrib><creatorcontrib>Rammelt, Stefan</creatorcontrib><creatorcontrib>Egerbacher, Monika</creatorcontrib><creatorcontrib>Erben, Reinhold G</creatorcontrib><creatorcontrib>Jessberger, Rolf</creatorcontrib><title>Regulation of bone mass and osteoclast function depend on the F-actin modulator SWAP-70</title><title>Journal of bone and mineral research</title><addtitle>J Bone Miner Res</addtitle><description>Bone remodeling involves tightly regulated bone‐resorbing osteoclasts and bone‐forming osteoblasts. Determining osteoclast function is central to understanding bone diseases such as osteoporosis and osteopetrosis. Here, we report a novel function of the F‐actin binding and regulatory protein SWAP‐70 in osteoclast biology. F‐actin ring formation, cell morphology, and bone resorption are impaired in Swap‐70−/− osteoclasts, whereas the expression of osteoclast differentiation markers induced in vitro by macrophage colony‐stimulating factor (M‐CSF) and receptor activator of NF‐κB ligand (RANKL) remains unaffected. Swap‐70−/− mice develop osteopetrosis with increased bone mass, abnormally dense bone, and impaired osteoclast function. Ectopic expression of SWAP‐70 in Swap‐70−/− osteoclasts in vitro rescues their deficiencies in bone resorption and F‐actin ring formation. Rescue requires a functional pleckstrin homology (PH) domain, known to support membrane localization of SWAP‐70, and the F‐actin binding domain. Transplantation of SWAP‐70–proficient bone marrow into Swap‐70−/− mice restores osteoclast resorption capacity in vivo. The identification of the role of SWAP‐70 in promoting osteoclast function through modulating membrane‐proximal F‐actin rearrangements reveals a new pathway to control osteoclasts and bone homeostasis. © 2012 American Society for Bone and Mineral Research.</description><subject>Actins - metabolism</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>BONE</subject><subject>Bone and Bones - pathology</subject><subject>Bone Resorption - complications</subject><subject>Bone Resorption - pathology</subject><subject>Cell Line</subject><subject>Cell Movement</subject><subject>DNA-Binding Proteins - deficiency</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>F-ACTIN</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>Guanine Nucleotide Exchange Factors - deficiency</topic><topic>Guanine Nucleotide Exchange Factors - metabolism</topic><topic>Humans</topic><topic>Indexing in process</topic><topic>Mice</topic><topic>Minor Histocompatibility Antigens</topic><topic>Nuclear Proteins - deficiency</topic><topic>Nuclear Proteins - metabolism</topic><topic>Organ Size</topic><topic>Osteoblasts - pathology</topic><topic>OSTEOCLASTS</topic><topic>Osteoclasts - metabolism</topic><topic>Osteoclasts - pathology</topic><topic>Osteopetrosis - complications</topic><topic>Osteopetrosis - pathology</topic><topic>RESORPTION</topic><topic>Skeleton and joints</topic><topic>SWAP-70</topic><topic>Vertebrates: osteoarticular system, musculoskeletal system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garbe, Annette I</creatorcontrib><creatorcontrib>Roscher, Anne</creatorcontrib><creatorcontrib>Schüler, Christiane</creatorcontrib><creatorcontrib>Lutter, Anne-Helen</creatorcontrib><creatorcontrib>Glösmann, Martin</creatorcontrib><creatorcontrib>Bernhardt, Ricardo</creatorcontrib><creatorcontrib>Chopin, Michael</creatorcontrib><creatorcontrib>Hempel, Ute</creatorcontrib><creatorcontrib>Hofbauer, Lorenz C</creatorcontrib><creatorcontrib>Rammelt, Stefan</creatorcontrib><creatorcontrib>Egerbacher, Monika</creatorcontrib><creatorcontrib>Erben, Reinhold G</creatorcontrib><creatorcontrib>Jessberger, Rolf</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of bone and mineral research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garbe, Annette I</au><au>Roscher, Anne</au><au>Schüler, Christiane</au><au>Lutter, Anne-Helen</au><au>Glösmann, Martin</au><au>Bernhardt, Ricardo</au><au>Chopin, Michael</au><au>Hempel, Ute</au><au>Hofbauer, Lorenz C</au><au>Rammelt, Stefan</au><au>Egerbacher, Monika</au><au>Erben, Reinhold G</au><au>Jessberger, Rolf</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of bone mass and osteoclast function depend on the F-actin modulator SWAP-70</atitle><jtitle>Journal of bone and mineral research</jtitle><addtitle>J Bone Miner Res</addtitle><date>2012-10</date><risdate>2012</risdate><volume>27</volume><issue>10</issue><spage>2085</spage><epage>2096</epage><pages>2085-2096</pages><issn>0884-0431</issn><eissn>1523-4681</eissn><coden>JBMREJ</coden><abstract>Bone remodeling involves tightly regulated bone‐resorbing osteoclasts and bone‐forming osteoblasts. Determining osteoclast function is central to understanding bone diseases such as osteoporosis and osteopetrosis. Here, we report a novel function of the F‐actin binding and regulatory protein SWAP‐70 in osteoclast biology. F‐actin ring formation, cell morphology, and bone resorption are impaired in Swap‐70−/− osteoclasts, whereas the expression of osteoclast differentiation markers induced in vitro by macrophage colony‐stimulating factor (M‐CSF) and receptor activator of NF‐κB ligand (RANKL) remains unaffected. Swap‐70−/− mice develop osteopetrosis with increased bone mass, abnormally dense bone, and impaired osteoclast function. Ectopic expression of SWAP‐70 in Swap‐70−/− osteoclasts in vitro rescues their deficiencies in bone resorption and F‐actin ring formation. Rescue requires a functional pleckstrin homology (PH) domain, known to support membrane localization of SWAP‐70, and the F‐actin binding domain. Transplantation of SWAP‐70–proficient bone marrow into Swap‐70−/− mice restores osteoclast resorption capacity in vivo. The identification of the role of SWAP‐70 in promoting osteoclast function through modulating membrane‐proximal F‐actin rearrangements reveals a new pathway to control osteoclasts and bone homeostasis. © 2012 American Society for Bone and Mineral Research.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22648978</pmid><doi>10.1002/jbmr.1670</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actins - metabolism Animals Biological and medical sciences BONE Bone and Bones - pathology Bone Resorption - complications Bone Resorption - pathology Cell Line Cell Movement DNA-Binding Proteins - deficiency DNA-Binding Proteins - metabolism F-ACTIN Fundamental and applied biological sciences. Psychology Guanine Nucleotide Exchange Factors - deficiency Guanine Nucleotide Exchange Factors - metabolism Humans Indexing in process Mice Minor Histocompatibility Antigens Nuclear Proteins - deficiency Nuclear Proteins - metabolism Organ Size Osteoblasts - pathology OSTEOCLASTS Osteoclasts - metabolism Osteoclasts - pathology Osteopetrosis - complications Osteopetrosis - pathology RESORPTION Skeleton and joints SWAP-70 Vertebrates: osteoarticular system, musculoskeletal system |
title | Regulation of bone mass and osteoclast function depend on the F-actin modulator SWAP-70 |
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