Thrombospondins and Novel TSR-containing Proteins, R-spondins, Regulate Bone Formation and Remodeling
Thrombospondins (TSPs) are a family of five secreted multimeric matricellular proteins that share homology in the type II and III repeats and carboxy-terminal region. Type I repeats, also known as properdin or thrombospondin repeats (TSRs), are found in TSP1/2, but not TSP3-5. A variety of other sec...
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description | Thrombospondins (TSPs) are a family of five secreted multimeric matricellular proteins that share homology in the type II and III repeats and carboxy-terminal region. Type I repeats, also known as properdin or thrombospondin repeats (TSRs), are found in TSP1/2, but not TSP3-5. A variety of other secreted proteins contain TSRs, including the novel extracellular molecules, R-spondins. TSP family and many TSR-containing proteins, including R-spondins, are highly expressed in skeletal tissues during development and postnatal. TSP2 regulates the osteoblast lineage, influencing bone mass and geometry, as well as response to fracture healing, ovariectomy, and mechanical loading. Compound knockout mice of TSPs have revealed important mechanistic insights. TSP1/2 knockout mice have craniofacial dysmorphism, and TSP1/3/5 compound knockout mice display growth plate abnormalities. R-spondins promote osteoblast differentiation and R-spondin-2 deficiency results in skeletal developmental defects. Overall, TSP and other TSR molecules influence multiple aspects of bone development and remodeling. |
doi_str_mv | 10.1007/s11914-010-0017-0 |
format | Article |
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Type I repeats, also known as properdin or thrombospondin repeats (TSRs), are found in TSP1/2, but not TSP3-5. A variety of other secreted proteins contain TSRs, including the novel extracellular molecules, R-spondins. TSP family and many TSR-containing proteins, including R-spondins, are highly expressed in skeletal tissues during development and postnatal. TSP2 regulates the osteoblast lineage, influencing bone mass and geometry, as well as response to fracture healing, ovariectomy, and mechanical loading. Compound knockout mice of TSPs have revealed important mechanistic insights. TSP1/2 knockout mice have craniofacial dysmorphism, and TSP1/3/5 compound knockout mice display growth plate abnormalities. R-spondins promote osteoblast differentiation and R-spondin-2 deficiency results in skeletal developmental defects. 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Type I repeats, also known as properdin or thrombospondin repeats (TSRs), are found in TSP1/2, but not TSP3-5. A variety of other secreted proteins contain TSRs, including the novel extracellular molecules, R-spondins. TSP family and many TSR-containing proteins, including R-spondins, are highly expressed in skeletal tissues during development and postnatal. TSP2 regulates the osteoblast lineage, influencing bone mass and geometry, as well as response to fracture healing, ovariectomy, and mechanical loading. Compound knockout mice of TSPs have revealed important mechanistic insights. TSP1/2 knockout mice have craniofacial dysmorphism, and TSP1/3/5 compound knockout mice display growth plate abnormalities. R-spondins promote osteoblast differentiation and R-spondin-2 deficiency results in skeletal developmental defects. Overall, TSP and other TSR molecules influence multiple aspects of bone development and remodeling.</description><subject>Animals</subject><subject>Bone and Bones - cytology</subject><subject>Bone and Bones - metabolism</subject><subject>Bone Regeneration - physiology</subject><subject>Bone Remodeling - physiology</subject><subject>Epidemiology</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Orthopedics</subject><subject>Osteoblasts - metabolism</subject><subject>Thrombospondins - metabolism</subject><issn>1544-1873</issn><issn>1544-2241</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqXwAWxQdmwwePxomiVUFJAqQKWsLSd2SqrELnaCxN_jkpYlqxlpzr3SHITOgVwDIelNAMiAYwIEEwIpJgdoCIJzTCmHw90Ok5QN0EkIa0IoBc6O0YASTsUY2BCZ5Yd3Te7Cxlld2ZAoq5Nn92XqZPm2wIWzrapsZVfJq3eticRVssB7Ou5m1dWqNcmdsyaZOd-otnL2t2ZhGqdNHcOn6KhUdTBnuzlC77P75fQRz18enqa3c1wwygnOMs3KXGmeT0SRaip0pgUfEw18olPgIEpRApQpm4zLssgFz6FQWpBUjXMFho3QZd-78e6zM6GVTRUKU9fKGtcFmTKWUU6piCT0ZOFdCN6UcuOrRvlvCURu5cperoxy5VauJDFzsWvv8sbov8TeZgRoD4R4sivj5dp13saP_2n9AUpMhQM</recordid><startdate>201006</startdate><enddate>201006</enddate><creator>Hankenson, Kurt D.</creator><creator>Sweetwyne, Mariya T.</creator><creator>Shitaye, Hailu</creator><creator>Posey, Karen L.</creator><general>Current Science Inc</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>7X8</scope></search><sort><creationdate>201006</creationdate><title>Thrombospondins and Novel TSR-containing Proteins, R-spondins, Regulate Bone Formation and Remodeling</title><author>Hankenson, Kurt D. ; Sweetwyne, Mariya T. ; Shitaye, Hailu ; Posey, Karen L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3240-99d3fbad4b85c7d25d9d5460d148d71415f5f11f7386ffcb54b1cad507a6ba1e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Bone and Bones - cytology</topic><topic>Bone and Bones - metabolism</topic><topic>Bone Regeneration - physiology</topic><topic>Bone Remodeling - physiology</topic><topic>Epidemiology</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Orthopedics</topic><topic>Osteoblasts - metabolism</topic><topic>Thrombospondins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hankenson, Kurt D.</creatorcontrib><creatorcontrib>Sweetwyne, Mariya T.</creatorcontrib><creatorcontrib>Shitaye, Hailu</creatorcontrib><creatorcontrib>Posey, Karen L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Current osteoporosis reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hankenson, Kurt D.</au><au>Sweetwyne, Mariya T.</au><au>Shitaye, Hailu</au><au>Posey, Karen L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thrombospondins and Novel TSR-containing Proteins, R-spondins, Regulate Bone Formation and Remodeling</atitle><jtitle>Current osteoporosis reports</jtitle><stitle>Curr Osteoporos Rep</stitle><addtitle>Curr Osteoporos Rep</addtitle><date>2010-06</date><risdate>2010</risdate><volume>8</volume><issue>2</issue><spage>68</spage><epage>76</epage><pages>68-76</pages><issn>1544-1873</issn><eissn>1544-2241</eissn><abstract>Thrombospondins (TSPs) are a family of five secreted multimeric matricellular proteins that share homology in the type II and III repeats and carboxy-terminal region. Type I repeats, also known as properdin or thrombospondin repeats (TSRs), are found in TSP1/2, but not TSP3-5. A variety of other secreted proteins contain TSRs, including the novel extracellular molecules, R-spondins. TSP family and many TSR-containing proteins, including R-spondins, are highly expressed in skeletal tissues during development and postnatal. TSP2 regulates the osteoblast lineage, influencing bone mass and geometry, as well as response to fracture healing, ovariectomy, and mechanical loading. Compound knockout mice of TSPs have revealed important mechanistic insights. TSP1/2 knockout mice have craniofacial dysmorphism, and TSP1/3/5 compound knockout mice display growth plate abnormalities. R-spondins promote osteoblast differentiation and R-spondin-2 deficiency results in skeletal developmental defects. Overall, TSP and other TSR molecules influence multiple aspects of bone development and remodeling.</abstract><cop>New York</cop><pub>Current Science Inc</pub><pmid>20425613</pmid><doi>10.1007/s11914-010-0017-0</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Bone and Bones - cytology Bone and Bones - metabolism Bone Regeneration - physiology Bone Remodeling - physiology Epidemiology Humans Medicine Medicine & Public Health Orthopedics Osteoblasts - metabolism Thrombospondins - metabolism |
title | Thrombospondins and Novel TSR-containing Proteins, R-spondins, Regulate Bone Formation and Remodeling |
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