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Disruption of LRP6 in osteoblasts blunts the bone anabolic activity of PTH
ABSTRACT Mutations in low‐density lipoprotein receptor‐related protein 6 (LRP6) are associated with human skeletal disorders. LRP6 is required for parathyroid hormone (PTH)‐stimulated signaling pathways in osteoblasts. We investigated whether LRP6 in osteoblasts directly regulates bone remodeling an...
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Published in: | Journal of bone and mineral research 2013-10, Vol.28 (10), p.2094-2108 |
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container_title | Journal of bone and mineral research |
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creator | Li, Changjun Xing, Qiujuan Yu, Bing Xie, Hui Wang, Weishan Shi, Chenhui Crane, Janet L Cao, Xu Wan, Mei |
description | ABSTRACT
Mutations in low‐density lipoprotein receptor‐related protein 6 (LRP6) are associated with human skeletal disorders. LRP6 is required for parathyroid hormone (PTH)‐stimulated signaling pathways in osteoblasts. We investigated whether LRP6 in osteoblasts directly regulates bone remodeling and mediates the bone anabolic effects of PTH by specifically deleting LRP6 in mature osteoblasts in mice (LRP6 KO). Three‐month‐old LRP6 KO mice had a significant reduction in bone mass in the femora secondary spongiosa relative to their wild‐type littermates, whereas marginal changes were found in femoral tissue of 1‐month‐old LRP6 KO mice. The remodeling area of the 3‐month‐old LRP6 KO mice showed a decreased bone formation rate as detected by Goldner's Trichrome staining and calcein double labeling. Bone histomorphometric and immumohistochemical analysis revealed a reduction in osteoblasts but little change in the numbers of osteoclasts and osteoprogenitors/osteoblast precursors in LRP6 KO mice compared with wild‐type littermates. In addition, the percentage of the apoptotic osteoblasts on the bone surface was higher in LRP6 KO mice compared with wild‐type littermates. Intermittent injection of PTH had no effect on bone mass or osteoblastic bone formation in either trabecular and cortical bone in LRP6 KO mice, whereas all were enhanced in wild‐type littermates. Additionally, the anti‐apoptotic effect of PTH on osteoblasts in LRP6 KO mice was less significant compared with wild‐type mice. Therefore, our findings demonstrate that LRP6 in osteoblasts is essential for osteoblastic differentiation during bone remodeling and the anabolic effects of PTH. © 2013 American Society for Bone and Mineral Research. |
doi_str_mv | 10.1002/jbmr.1962 |
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Mutations in low‐density lipoprotein receptor‐related protein 6 (LRP6) are associated with human skeletal disorders. LRP6 is required for parathyroid hormone (PTH)‐stimulated signaling pathways in osteoblasts. We investigated whether LRP6 in osteoblasts directly regulates bone remodeling and mediates the bone anabolic effects of PTH by specifically deleting LRP6 in mature osteoblasts in mice (LRP6 KO). Three‐month‐old LRP6 KO mice had a significant reduction in bone mass in the femora secondary spongiosa relative to their wild‐type littermates, whereas marginal changes were found in femoral tissue of 1‐month‐old LRP6 KO mice. The remodeling area of the 3‐month‐old LRP6 KO mice showed a decreased bone formation rate as detected by Goldner's Trichrome staining and calcein double labeling. Bone histomorphometric and immumohistochemical analysis revealed a reduction in osteoblasts but little change in the numbers of osteoclasts and osteoprogenitors/osteoblast precursors in LRP6 KO mice compared with wild‐type littermates. In addition, the percentage of the apoptotic osteoblasts on the bone surface was higher in LRP6 KO mice compared with wild‐type littermates. Intermittent injection of PTH had no effect on bone mass or osteoblastic bone formation in either trabecular and cortical bone in LRP6 KO mice, whereas all were enhanced in wild‐type littermates. Additionally, the anti‐apoptotic effect of PTH on osteoblasts in LRP6 KO mice was less significant compared with wild‐type mice. Therefore, our findings demonstrate that LRP6 in osteoblasts is essential for osteoblastic differentiation during bone remodeling and the anabolic effects of PTH. © 2013 American Society for Bone and Mineral Research.</description><identifier>ISSN: 0884-0431</identifier><identifier>EISSN: 1523-4681</identifier><identifier>DOI: 10.1002/jbmr.1962</identifier><identifier>PMID: 23609180</identifier><identifier>CODEN: JBMREJ</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Anabolic Agents - pharmacology ; Animals ; Apoptosis - drug effects ; Apoptosis - genetics ; beta Catenin - metabolism ; Bone and Bones - drug effects ; Bone and Bones - metabolism ; Bone and Bones - pathology ; BONE REMODELING ; Bone Remodeling - drug effects ; Bone Remodeling - genetics ; Bone Resorption - metabolism ; Bone Resorption - pathology ; Bone Resorption - physiopathology ; Cell Differentiation - drug effects ; Cell Differentiation - genetics ; Cyclic AMP-Dependent Protein Kinases - metabolism ; Gene Deletion ; Gene Expression Regulation - drug effects ; GTP-Binding Protein alpha Subunits - metabolism ; Humans ; Integrases - metabolism ; Low Density Lipoprotein Receptor-Related Protein-6 - deficiency ; Low Density Lipoprotein Receptor-Related Protein-6 - metabolism ; LRP6 ; Mice ; Mice, Knockout ; Organ Size - drug effects ; OSTEOBLAST APOPTOSIS ; OSTEOBLAST DIFFERENTIATION ; Osteoblasts - drug effects ; Osteoblasts - metabolism ; Osteoblasts - pathology ; Osteogenesis - drug effects ; Parathyroid Hormone - pharmacology ; Phenotype ; PTH ; Signal Transduction - drug effects ; Signal Transduction - genetics</subject><ispartof>Journal of bone and mineral research, 2013-10, Vol.28 (10), p.2094-2108</ispartof><rights>2013 American Society for Bone and Mineral Research</rights><rights>2013 American Society for Bone and Mineral Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5422-aa430cb44ae257d3865d7adf0beef9c753549ced0f77b5169542987c36b3de763</citedby><cites>FETCH-LOGICAL-c5422-aa430cb44ae257d3865d7adf0beef9c753549ced0f77b5169542987c36b3de763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23609180$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Changjun</creatorcontrib><creatorcontrib>Xing, Qiujuan</creatorcontrib><creatorcontrib>Yu, Bing</creatorcontrib><creatorcontrib>Xie, Hui</creatorcontrib><creatorcontrib>Wang, Weishan</creatorcontrib><creatorcontrib>Shi, Chenhui</creatorcontrib><creatorcontrib>Crane, Janet L</creatorcontrib><creatorcontrib>Cao, Xu</creatorcontrib><creatorcontrib>Wan, Mei</creatorcontrib><title>Disruption of LRP6 in osteoblasts blunts the bone anabolic activity of PTH</title><title>Journal of bone and mineral research</title><addtitle>J Bone Miner Res</addtitle><description>ABSTRACT
Mutations in low‐density lipoprotein receptor‐related protein 6 (LRP6) are associated with human skeletal disorders. LRP6 is required for parathyroid hormone (PTH)‐stimulated signaling pathways in osteoblasts. We investigated whether LRP6 in osteoblasts directly regulates bone remodeling and mediates the bone anabolic effects of PTH by specifically deleting LRP6 in mature osteoblasts in mice (LRP6 KO). Three‐month‐old LRP6 KO mice had a significant reduction in bone mass in the femora secondary spongiosa relative to their wild‐type littermates, whereas marginal changes were found in femoral tissue of 1‐month‐old LRP6 KO mice. The remodeling area of the 3‐month‐old LRP6 KO mice showed a decreased bone formation rate as detected by Goldner's Trichrome staining and calcein double labeling. Bone histomorphometric and immumohistochemical analysis revealed a reduction in osteoblasts but little change in the numbers of osteoclasts and osteoprogenitors/osteoblast precursors in LRP6 KO mice compared with wild‐type littermates. In addition, the percentage of the apoptotic osteoblasts on the bone surface was higher in LRP6 KO mice compared with wild‐type littermates. Intermittent injection of PTH had no effect on bone mass or osteoblastic bone formation in either trabecular and cortical bone in LRP6 KO mice, whereas all were enhanced in wild‐type littermates. Additionally, the anti‐apoptotic effect of PTH on osteoblasts in LRP6 KO mice was less significant compared with wild‐type mice. Therefore, our findings demonstrate that LRP6 in osteoblasts is essential for osteoblastic differentiation during bone remodeling and the anabolic effects of PTH. © 2013 American Society for Bone and Mineral Research.</description><subject>Anabolic Agents - pharmacology</subject><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis - genetics</subject><subject>beta Catenin - metabolism</subject><subject>Bone and Bones - drug effects</subject><subject>Bone and Bones - metabolism</subject><subject>Bone and Bones - pathology</subject><subject>BONE REMODELING</subject><subject>Bone Remodeling - drug effects</subject><subject>Bone Remodeling - genetics</subject><subject>Bone Resorption - metabolism</subject><subject>Bone Resorption - pathology</subject><subject>Bone Resorption - physiopathology</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Differentiation - genetics</subject><subject>Cyclic AMP-Dependent Protein Kinases - metabolism</subject><subject>Gene Deletion</subject><subject>Gene Expression Regulation - drug effects</subject><subject>GTP-Binding Protein alpha Subunits - metabolism</subject><subject>Humans</subject><subject>Integrases - metabolism</subject><subject>Low Density Lipoprotein Receptor-Related Protein-6 - deficiency</subject><subject>Low Density Lipoprotein Receptor-Related Protein-6 - metabolism</subject><subject>LRP6</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Organ Size - drug effects</subject><subject>OSTEOBLAST APOPTOSIS</subject><subject>OSTEOBLAST DIFFERENTIATION</subject><subject>Osteoblasts - drug effects</subject><subject>Osteoblasts - metabolism</subject><subject>Osteoblasts - pathology</subject><subject>Osteogenesis - drug effects</subject><subject>Parathyroid Hormone - pharmacology</subject><subject>Phenotype</subject><subject>PTH</subject><subject>Signal Transduction - drug effects</subject><subject>Signal Transduction - genetics</subject><issn>0884-0431</issn><issn>1523-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kU1P3DAQhi1UBFvaA38AReqlHAJ2xl-5VGqXb21VhOBs2Y5TvMrGi51Q7b-vlwUElXqakeaZRzN6Edon-IhgXB3PzSIekZpXW2hCWAUl5ZJ8QBMsJS0xBbKLPqY0xxhzxvkO2q2A45pIPEFXJz7FcTn40BehLWY317zwuU2DC6bTaUiF6cY-l-HeFSb0rtC9NqHzttB28I9-WK0Xr28vPqHtVnfJfX6ue-ju7PR2elHOfp1fTr_PSstoVZVaU8DWUKpdxUQDkrNG6KbFxrm2toIBo7V1DW6FMIzwOm_VUljgBhonOOyhbxvvcjQL11jXD1F3ahn9QseVCtqr95Pe36vf4VGBkEIQyIKvz4IYHkaXBrXwybqu070LY1KEUgDBBGMZ_fIPOg9j7PN7mQIAKSTUmTrcUDaGlKJrX48hWK0TUuuE1DqhzB68vf6VfIkkA8cb4I_v3Or_JnX14-fNk_IvjN2a5Q</recordid><startdate>201310</startdate><enddate>201310</enddate><creator>Li, Changjun</creator><creator>Xing, Qiujuan</creator><creator>Yu, Bing</creator><creator>Xie, Hui</creator><creator>Wang, Weishan</creator><creator>Shi, Chenhui</creator><creator>Crane, Janet L</creator><creator>Cao, Xu</creator><creator>Wan, Mei</creator><general>Wiley Subscription Services, 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>7QP</scope><scope>7TS</scope><scope>K9.</scope><scope>5PM</scope></search><sort><creationdate>201310</creationdate><title>Disruption of LRP6 in osteoblasts blunts the bone anabolic activity of PTH</title><author>Li, Changjun ; Xing, Qiujuan ; Yu, Bing ; Xie, Hui ; Wang, Weishan ; Shi, Chenhui ; Crane, Janet L ; Cao, Xu ; Wan, Mei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5422-aa430cb44ae257d3865d7adf0beef9c753549ced0f77b5169542987c36b3de763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Anabolic Agents - pharmacology</topic><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Apoptosis - genetics</topic><topic>beta Catenin - metabolism</topic><topic>Bone and Bones - drug effects</topic><topic>Bone and Bones - metabolism</topic><topic>Bone and Bones - pathology</topic><topic>BONE REMODELING</topic><topic>Bone Remodeling - drug effects</topic><topic>Bone Remodeling - genetics</topic><topic>Bone Resorption - metabolism</topic><topic>Bone Resorption - pathology</topic><topic>Bone Resorption - physiopathology</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Differentiation - genetics</topic><topic>Cyclic AMP-Dependent Protein Kinases - metabolism</topic><topic>Gene Deletion</topic><topic>Gene Expression Regulation - drug effects</topic><topic>GTP-Binding Protein alpha Subunits - metabolism</topic><topic>Humans</topic><topic>Integrases - metabolism</topic><topic>Low Density Lipoprotein Receptor-Related Protein-6 - deficiency</topic><topic>Low Density Lipoprotein Receptor-Related Protein-6 - metabolism</topic><topic>LRP6</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Organ Size - drug effects</topic><topic>OSTEOBLAST APOPTOSIS</topic><topic>OSTEOBLAST DIFFERENTIATION</topic><topic>Osteoblasts - drug effects</topic><topic>Osteoblasts - metabolism</topic><topic>Osteoblasts - pathology</topic><topic>Osteogenesis - drug effects</topic><topic>Parathyroid Hormone - pharmacology</topic><topic>Phenotype</topic><topic>PTH</topic><topic>Signal Transduction - drug effects</topic><topic>Signal Transduction - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Changjun</creatorcontrib><creatorcontrib>Xing, Qiujuan</creatorcontrib><creatorcontrib>Yu, Bing</creatorcontrib><creatorcontrib>Xie, Hui</creatorcontrib><creatorcontrib>Wang, Weishan</creatorcontrib><creatorcontrib>Shi, Chenhui</creatorcontrib><creatorcontrib>Crane, Janet L</creatorcontrib><creatorcontrib>Cao, Xu</creatorcontrib><creatorcontrib>Wan, Mei</creatorcontrib><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>PubMed Central (Full Participant titles)</collection><jtitle>Journal of bone and mineral research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Changjun</au><au>Xing, Qiujuan</au><au>Yu, Bing</au><au>Xie, Hui</au><au>Wang, Weishan</au><au>Shi, Chenhui</au><au>Crane, Janet L</au><au>Cao, Xu</au><au>Wan, Mei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Disruption of LRP6 in osteoblasts blunts the bone anabolic activity of PTH</atitle><jtitle>Journal of bone and mineral research</jtitle><addtitle>J Bone Miner Res</addtitle><date>2013-10</date><risdate>2013</risdate><volume>28</volume><issue>10</issue><spage>2094</spage><epage>2108</epage><pages>2094-2108</pages><issn>0884-0431</issn><eissn>1523-4681</eissn><coden>JBMREJ</coden><abstract>ABSTRACT
Mutations in low‐density lipoprotein receptor‐related protein 6 (LRP6) are associated with human skeletal disorders. LRP6 is required for parathyroid hormone (PTH)‐stimulated signaling pathways in osteoblasts. We investigated whether LRP6 in osteoblasts directly regulates bone remodeling and mediates the bone anabolic effects of PTH by specifically deleting LRP6 in mature osteoblasts in mice (LRP6 KO). Three‐month‐old LRP6 KO mice had a significant reduction in bone mass in the femora secondary spongiosa relative to their wild‐type littermates, whereas marginal changes were found in femoral tissue of 1‐month‐old LRP6 KO mice. The remodeling area of the 3‐month‐old LRP6 KO mice showed a decreased bone formation rate as detected by Goldner's Trichrome staining and calcein double labeling. Bone histomorphometric and immumohistochemical analysis revealed a reduction in osteoblasts but little change in the numbers of osteoclasts and osteoprogenitors/osteoblast precursors in LRP6 KO mice compared with wild‐type littermates. In addition, the percentage of the apoptotic osteoblasts on the bone surface was higher in LRP6 KO mice compared with wild‐type littermates. Intermittent injection of PTH had no effect on bone mass or osteoblastic bone formation in either trabecular and cortical bone in LRP6 KO mice, whereas all were enhanced in wild‐type littermates. Additionally, the anti‐apoptotic effect of PTH on osteoblasts in LRP6 KO mice was less significant compared with wild‐type mice. Therefore, our findings demonstrate that LRP6 in osteoblasts is essential for osteoblastic differentiation during bone remodeling and the anabolic effects of PTH. © 2013 American Society for Bone and Mineral Research.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>23609180</pmid><doi>10.1002/jbmr.1962</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anabolic Agents - pharmacology Animals Apoptosis - drug effects Apoptosis - genetics beta Catenin - metabolism Bone and Bones - drug effects Bone and Bones - metabolism Bone and Bones - pathology BONE REMODELING Bone Remodeling - drug effects Bone Remodeling - genetics Bone Resorption - metabolism Bone Resorption - pathology Bone Resorption - physiopathology Cell Differentiation - drug effects Cell Differentiation - genetics Cyclic AMP-Dependent Protein Kinases - metabolism Gene Deletion Gene Expression Regulation - drug effects GTP-Binding Protein alpha Subunits - metabolism Humans Integrases - metabolism Low Density Lipoprotein Receptor-Related Protein-6 - deficiency Low Density Lipoprotein Receptor-Related Protein-6 - metabolism LRP6 Mice Mice, Knockout Organ Size - drug effects OSTEOBLAST APOPTOSIS OSTEOBLAST DIFFERENTIATION Osteoblasts - drug effects Osteoblasts - metabolism Osteoblasts - pathology Osteogenesis - drug effects Parathyroid Hormone - pharmacology Phenotype PTH Signal Transduction - drug effects Signal Transduction - genetics |
title | Disruption of LRP6 in osteoblasts blunts the bone anabolic activity of PTH |
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