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Transgenic mice with osteoblast-targeted insulin-like growth factor-I show increased bone remodeling
To determine the effects of locally-expressed insulin-like growth factor (IGF-I) on bone remodeling, a transgene was produced in which murine IGF-I cDNA was cloned downstream of a gene fragment comprising 3.6 kb of 5′ upstream regulatory sequence and most of the first intron of the rat Col1a1 gene....
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Published in: | Bone (New York, N.Y.) N.Y.), 2006-09, Vol.39 (3), p.494-504 |
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creator | Jiang, Jin Lichtler, Alexander C. Gronowicz, Gloria A. Adams, Douglas J. Clark, Stephen H. Rosen, Clifford J. Kream, Barbara E. |
description | To determine the effects of locally-expressed insulin-like growth factor (IGF-I) on bone remodeling, a transgene was produced in which murine IGF-I cDNA was cloned downstream of a gene fragment comprising 3.6 kb of 5′ upstream regulatory sequence and most of the first intron of the rat Col1a1 gene. The construct was expressed at the mRNA and protein level in transfected osteoblasts. Five lines of transgenic mice were generated by embryo microinjection. Transgene mRNA levels were highest in calvaria, long bone and tendon, and lower in skin. Serum IGF-I and body weight were increased in males and females only in the highest expressing line. Histomorphometry showed that transgenic calvaria were wider and had greater marrow area and bone area. Transgenic calvaria had increased osteoclast number per bone surface. Percent collagen synthesis and cell replication were increased in transgenic calvaria. Femur length, cortical width and cross-sectional area were increased in transgenic femurs of the highest expressing line, while femoral trabecular bone volume was little affected. Thus, broad overexpression of IGF-I in cells of the osteoblast lineage increased indices of bone formation and resorption. |
doi_str_mv | 10.1016/j.bone.2006.02.068 |
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The construct was expressed at the mRNA and protein level in transfected osteoblasts. Five lines of transgenic mice were generated by embryo microinjection. Transgene mRNA levels were highest in calvaria, long bone and tendon, and lower in skin. Serum IGF-I and body weight were increased in males and females only in the highest expressing line. Histomorphometry showed that transgenic calvaria were wider and had greater marrow area and bone area. Transgenic calvaria had increased osteoclast number per bone surface. Percent collagen synthesis and cell replication were increased in transgenic calvaria. Femur length, cortical width and cross-sectional area were increased in transgenic femurs of the highest expressing line, while femoral trabecular bone volume was little affected. Thus, broad overexpression of IGF-I in cells of the osteoblast lineage increased indices of bone formation and resorption.</description><identifier>ISSN: 8756-3282</identifier><identifier>EISSN: 1873-2763</identifier><identifier>DOI: 10.1016/j.bone.2006.02.068</identifier><identifier>PMID: 16644298</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Animals, Newborn ; Biological and medical sciences ; Body Weight ; Bone morphometry ; Bone remodeling ; Bone Remodeling - physiology ; Cell Line ; Cell Lineage ; Col1a1 promoter ; Female ; Femur - cytology ; Femur - metabolism ; Fundamental and applied biological sciences. Psychology ; Gene Expression ; IGF-I ; Insulin-Like Growth Factor I - genetics ; Insulin-Like Growth Factor I - metabolism ; Male ; Mice ; Mice, Transgenic ; Osteoblast ; Osteoblasts - metabolism ; Phenotype ; Rats ; Skeleton and joints ; Skull - anatomy & histology ; Skull - metabolism ; Tomography, Emission-Computed ; Transgenes - genetics ; Transgenic ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Vertebrates: osteoarticular system, musculoskeletal system</subject><ispartof>Bone (New York, N.Y.), 2006-09, Vol.39 (3), p.494-504</ispartof><rights>2006 Elsevier Inc.</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-e6eb31abfe8c0e2815c7014b44d9cadb73445be8b24c6ee9c4d7e8fe619d26e33</citedby><cites>FETCH-LOGICAL-c415t-e6eb31abfe8c0e2815c7014b44d9cadb73445be8b24c6ee9c4d7e8fe619d26e33</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=18050039$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16644298$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiang, Jin</creatorcontrib><creatorcontrib>Lichtler, Alexander C.</creatorcontrib><creatorcontrib>Gronowicz, Gloria A.</creatorcontrib><creatorcontrib>Adams, Douglas J.</creatorcontrib><creatorcontrib>Clark, Stephen H.</creatorcontrib><creatorcontrib>Rosen, Clifford J.</creatorcontrib><creatorcontrib>Kream, Barbara E.</creatorcontrib><title>Transgenic mice with osteoblast-targeted insulin-like growth factor-I show increased bone remodeling</title><title>Bone (New York, N.Y.)</title><addtitle>Bone</addtitle><description>To determine the effects of locally-expressed insulin-like growth factor (IGF-I) on bone remodeling, a transgene was produced in which murine IGF-I cDNA was cloned downstream of a gene fragment comprising 3.6 kb of 5′ upstream regulatory sequence and most of the first intron of the rat Col1a1 gene. The construct was expressed at the mRNA and protein level in transfected osteoblasts. Five lines of transgenic mice were generated by embryo microinjection. Transgene mRNA levels were highest in calvaria, long bone and tendon, and lower in skin. Serum IGF-I and body weight were increased in males and females only in the highest expressing line. Histomorphometry showed that transgenic calvaria were wider and had greater marrow area and bone area. Transgenic calvaria had increased osteoclast number per bone surface. Percent collagen synthesis and cell replication were increased in transgenic calvaria. Femur length, cortical width and cross-sectional area were increased in transgenic femurs of the highest expressing line, while femoral trabecular bone volume was little affected. Thus, broad overexpression of IGF-I in cells of the osteoblast lineage increased indices of bone formation and resorption.</description><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Biological and medical sciences</subject><subject>Body Weight</subject><subject>Bone morphometry</subject><subject>Bone remodeling</subject><subject>Bone Remodeling - physiology</subject><subject>Cell Line</subject><subject>Cell Lineage</subject><subject>Col1a1 promoter</subject><subject>Female</subject><subject>Femur - cytology</subject><subject>Femur - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression</subject><subject>IGF-I</subject><subject>Insulin-Like Growth Factor I - genetics</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Osteoblast</subject><subject>Osteoblasts - metabolism</subject><subject>Phenotype</subject><subject>Rats</subject><subject>Skeleton and joints</subject><subject>Skull - anatomy & histology</subject><subject>Skull - metabolism</subject><subject>Tomography, Emission-Computed</subject><subject>Transgenes - genetics</subject><subject>Transgenic</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Vertebrates: osteoarticular system, musculoskeletal system</subject><issn>8756-3282</issn><issn>1873-2763</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqF0ctu1DAUBmCrAtFp4QW6QNnALqlvsR2JDaqAVqrEpqwtX06mHpK42J6O-vY4mpG6g5U33390fH6ErgjuCCbietfZuEBHMRYdph0W6gxtiJKspVKwN2ijZC9aRhU9Rxc57zDGbJDkHTonQnBOB7VB_iGZJW9hCa6Zg4PmEMpjE3OBaCeTS1tM2kIB34Ql76ewtFP4Dc02xUN1o3ElpvauyY_xUIVLYHK1615Ngjl6qJHte_R2NFOGD6f3Ev36_u3h5ra9__nj7ubrfes46UsLAiwjxo6gHAaqSO8kJtxy7gdnvJWM896CspQ7ATA47iWoEQQZPBXA2CX6fJz7lOKfPeSi55AdTJNZIO6zFkriQVL5X0gGxQQTokJ6hC7FnBOM-imF2aQXTbBeS9A7vX5WryVoTHUtoYY-nqbv7Qz-NXK6egWfTsBkZ6axVuBCfnUK92tV1X05OqhHew6QdHYBFgc-JHBF-xj-tcdfHOGngg</recordid><startdate>20060901</startdate><enddate>20060901</enddate><creator>Jiang, Jin</creator><creator>Lichtler, Alexander C.</creator><creator>Gronowicz, Gloria A.</creator><creator>Adams, Douglas J.</creator><creator>Clark, Stephen H.</creator><creator>Rosen, Clifford J.</creator><creator>Kream, Barbara E.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><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>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20060901</creationdate><title>Transgenic mice with osteoblast-targeted insulin-like growth factor-I show increased bone remodeling</title><author>Jiang, Jin ; Lichtler, Alexander C. ; Gronowicz, Gloria A. ; Adams, Douglas J. ; Clark, Stephen H. ; Rosen, Clifford J. ; Kream, Barbara E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-e6eb31abfe8c0e2815c7014b44d9cadb73445be8b24c6ee9c4d7e8fe619d26e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biological and medical sciences</topic><topic>Body Weight</topic><topic>Bone morphometry</topic><topic>Bone remodeling</topic><topic>Bone Remodeling - physiology</topic><topic>Cell Line</topic><topic>Cell Lineage</topic><topic>Col1a1 promoter</topic><topic>Female</topic><topic>Femur - cytology</topic><topic>Femur - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression</topic><topic>IGF-I</topic><topic>Insulin-Like Growth Factor I - genetics</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Osteoblast</topic><topic>Osteoblasts - metabolism</topic><topic>Phenotype</topic><topic>Rats</topic><topic>Skeleton and joints</topic><topic>Skull - anatomy & histology</topic><topic>Skull - metabolism</topic><topic>Tomography, Emission-Computed</topic><topic>Transgenes - genetics</topic><topic>Transgenic</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Vertebrates: osteoarticular system, musculoskeletal system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiang, Jin</creatorcontrib><creatorcontrib>Lichtler, Alexander C.</creatorcontrib><creatorcontrib>Gronowicz, Gloria A.</creatorcontrib><creatorcontrib>Adams, Douglas J.</creatorcontrib><creatorcontrib>Clark, Stephen H.</creatorcontrib><creatorcontrib>Rosen, Clifford J.</creatorcontrib><creatorcontrib>Kream, Barbara E.</creatorcontrib><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>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Bone (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiang, Jin</au><au>Lichtler, Alexander C.</au><au>Gronowicz, Gloria A.</au><au>Adams, Douglas J.</au><au>Clark, Stephen H.</au><au>Rosen, Clifford J.</au><au>Kream, Barbara E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transgenic mice with osteoblast-targeted insulin-like growth factor-I show increased bone remodeling</atitle><jtitle>Bone (New York, N.Y.)</jtitle><addtitle>Bone</addtitle><date>2006-09-01</date><risdate>2006</risdate><volume>39</volume><issue>3</issue><spage>494</spage><epage>504</epage><pages>494-504</pages><issn>8756-3282</issn><eissn>1873-2763</eissn><abstract>To determine the effects of locally-expressed insulin-like growth factor (IGF-I) on bone remodeling, a transgene was produced in which murine IGF-I cDNA was cloned downstream of a gene fragment comprising 3.6 kb of 5′ upstream regulatory sequence and most of the first intron of the rat Col1a1 gene. The construct was expressed at the mRNA and protein level in transfected osteoblasts. Five lines of transgenic mice were generated by embryo microinjection. Transgene mRNA levels were highest in calvaria, long bone and tendon, and lower in skin. Serum IGF-I and body weight were increased in males and females only in the highest expressing line. Histomorphometry showed that transgenic calvaria were wider and had greater marrow area and bone area. Transgenic calvaria had increased osteoclast number per bone surface. Percent collagen synthesis and cell replication were increased in transgenic calvaria. Femur length, cortical width and cross-sectional area were increased in transgenic femurs of the highest expressing line, while femoral trabecular bone volume was little affected. Thus, broad overexpression of IGF-I in cells of the osteoblast lineage increased indices of bone formation and resorption.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>16644298</pmid><doi>10.1016/j.bone.2006.02.068</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Animals, Newborn Biological and medical sciences Body Weight Bone morphometry Bone remodeling Bone Remodeling - physiology Cell Line Cell Lineage Col1a1 promoter Female Femur - cytology Femur - metabolism Fundamental and applied biological sciences. Psychology Gene Expression IGF-I Insulin-Like Growth Factor I - genetics Insulin-Like Growth Factor I - metabolism Male Mice Mice, Transgenic Osteoblast Osteoblasts - metabolism Phenotype Rats Skeleton and joints Skull - anatomy & histology Skull - metabolism Tomography, Emission-Computed Transgenes - genetics Transgenic Vertebrates: anatomy and physiology, studies on body, several organs or systems Vertebrates: osteoarticular system, musculoskeletal system |
title | Transgenic mice with osteoblast-targeted insulin-like growth factor-I show increased bone remodeling |
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