Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Journal of bone and mineral research 2013-10, Vol.28 (10), p.2094-2108
Main Authors: Li, Changjun, Xing, Qiujuan, Yu, Bing, Xie, Hui, Wang, Weishan, Shi, Chenhui, Crane, Janet L, Cao, Xu, Wan, Mei
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c5422-aa430cb44ae257d3865d7adf0beef9c753549ced0f77b5169542987c36b3de763
cites cdi_FETCH-LOGICAL-c5422-aa430cb44ae257d3865d7adf0beef9c753549ced0f77b5169542987c36b3de763
container_end_page 2108
container_issue 10
container_start_page 2094
container_title Journal of bone and mineral research
container_volume 28
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
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3787713</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1443375755</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5422-aa430cb44ae257d3865d7adf0beef9c753549ced0f77b5169542987c36b3de763</originalsourceid><addsrcrecordid>eNp1kU1P3DAQhi1UBFvaA38AReqlHAJ2xl-5VGqXb21VhOBs2Y5TvMrGi51Q7b-vlwUElXqakeaZRzN6Edon-IhgXB3PzSIekZpXW2hCWAUl5ZJ8QBMsJS0xBbKLPqY0xxhzxvkO2q2A45pIPEFXJz7FcTn40BehLWY317zwuU2DC6bTaUiF6cY-l-HeFSb0rtC9NqHzttB28I9-WK0Xr28vPqHtVnfJfX6ue-ju7PR2elHOfp1fTr_PSstoVZVaU8DWUKpdxUQDkrNG6KbFxrm2toIBo7V1DW6FMIzwOm_VUljgBhonOOyhbxvvcjQL11jXD1F3ahn9QseVCtqr95Pe36vf4VGBkEIQyIKvz4IYHkaXBrXwybqu070LY1KEUgDBBGMZ_fIPOg9j7PN7mQIAKSTUmTrcUDaGlKJrX48hWK0TUuuE1DqhzB68vf6VfIkkA8cb4I_v3Or_JnX14-fNk_IvjN2a5Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1433387839</pqid></control><display><type>article</type><title>Disruption of LRP6 in osteoblasts blunts the bone anabolic activity of PTH</title><source>Oxford Journals Online</source><creator>Li, Changjun ; Xing, Qiujuan ; Yu, Bing ; Xie, Hui ; Wang, Weishan ; Shi, Chenhui ; Crane, Janet L ; Cao, Xu ; Wan, Mei</creator><creatorcontrib>Li, Changjun ; Xing, Qiujuan ; Yu, Bing ; Xie, Hui ; Wang, Weishan ; Shi, Chenhui ; Crane, Janet L ; Cao, Xu ; Wan, Mei</creatorcontrib><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><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 &amp; Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>ProQuest Health &amp; 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>
fulltext fulltext
identifier ISSN: 0884-0431
ispartof Journal of bone and mineral research, 2013-10, Vol.28 (10), p.2094-2108
issn 0884-0431
1523-4681
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3787713
source Oxford Journals Online
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T18%3A59%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Disruption%20of%20LRP6%20in%20osteoblasts%20blunts%20the%20bone%20anabolic%20activity%20of%20PTH&rft.jtitle=Journal%20of%20bone%20and%20mineral%20research&rft.au=Li,%20Changjun&rft.date=2013-10&rft.volume=28&rft.issue=10&rft.spage=2094&rft.epage=2108&rft.pages=2094-2108&rft.issn=0884-0431&rft.eissn=1523-4681&rft.coden=JBMREJ&rft_id=info:doi/10.1002/jbmr.1962&rft_dat=%3Cproquest_pubme%3E1443375755%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5422-aa430cb44ae257d3865d7adf0beef9c753549ced0f77b5169542987c36b3de763%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1433387839&rft_id=info:pmid/23609180&rfr_iscdi=true