HES1 (Hairy and Enhancer of Split 1) Is a Determinant of Bone Mass
HES1 (hairy and enhancer of split) is a transcription factor that regulates osteoblastogenesis in vitro. The skeletal effects of HES1 misexpression were studied. Transgenic mice where a 3.6-kilobase fragment of the collagen type 1 α1 promoter directs HES1 overexpression were created. Transgenics wer...
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description | HES1 (hairy and enhancer of split) is a transcription factor that regulates osteoblastogenesis in vitro. The skeletal effects of HES1 misexpression were studied. Transgenic mice where a 3.6-kilobase fragment of the collagen type 1 α1 promoter directs HES1 overexpression were created. Transgenics were osteopenic due to decreased osteoblast function in female and increased bone resorption in male mice. HES1 impaired osteoblastogenesis in vitro, and transgenic osteoblasts enhanced the resorptive activity of co-cultured osteoclast precursors. Mice homozygous for a Hes1 loxP-targeted allele were bred to transgenics, where the paired-related homeobox gene enhancer or the osteocalcin promoter direct Cre recombinase expression to inactivate Hes1 in the limb bud or in osteoblasts. To avoid genetic compensation, Hes1 was inactivated in the context of the global deletion of Hes3 and Hes5. Hes3 and Hes5 null mice had no skeletal phenotype. Hes1 inactivation in the limb bud increased femoral length and trabecular number. Hes1 inactivation in osteoblasts increased trabecular bone volume, number, and connectivity due to increased mineral apposition rate and suppressed bone resorption. Hes1 inactivation in vitro increased alkaline phosphatase expression and suppressed the resorptive activity of co-cultured osteoclast precursors. In conclusion, by inhibiting osteoblast function and inducing bone resorption, HES1 is an intracellular determinant of bone mass and structure. |
doi_str_mv | 10.1074/jbc.M110.183038 |
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The skeletal effects of HES1 misexpression were studied. Transgenic mice where a 3.6-kilobase fragment of the collagen type 1 α1 promoter directs HES1 overexpression were created. Transgenics were osteopenic due to decreased osteoblast function in female and increased bone resorption in male mice. HES1 impaired osteoblastogenesis in vitro, and transgenic osteoblasts enhanced the resorptive activity of co-cultured osteoclast precursors. Mice homozygous for a Hes1 loxP-targeted allele were bred to transgenics, where the paired-related homeobox gene enhancer or the osteocalcin promoter direct Cre recombinase expression to inactivate Hes1 in the limb bud or in osteoblasts. To avoid genetic compensation, Hes1 was inactivated in the context of the global deletion of Hes3 and Hes5. Hes3 and Hes5 null mice had no skeletal phenotype. Hes1 inactivation in the limb bud increased femoral length and trabecular number. Hes1 inactivation in osteoblasts increased trabecular bone volume, number, and connectivity due to increased mineral apposition rate and suppressed bone resorption. Hes1 inactivation in vitro increased alkaline phosphatase expression and suppressed the resorptive activity of co-cultured osteoclast precursors. In conclusion, by inhibiting osteoblast function and inducing bone resorption, HES1 is an intracellular determinant of bone mass and structure.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M110.183038</identifier><identifier>PMID: 21084301</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alkaline Phosphatase - biosynthesis ; Alkaline Phosphatase - genetics ; Alleles ; Animals ; Basic Helix-Loop-Helix Transcription Factors - genetics ; Basic Helix-Loop-Helix Transcription Factors - metabolism ; Bone ; Bone Density - physiology ; Bone Diseases, Metabolic - genetics ; Bone Diseases, Metabolic - metabolism ; Bone Diseases, Metabolic - pathology ; Bone Formation ; Bone Resorption ; Cell Differentiation ; Cells, Cultured ; Coculture Techniques ; Collagen Type I - genetics ; Collagen Type I - metabolism ; Developmental Biology ; Enhancer Elements, Genetic - genetics ; Female ; Femur - metabolism ; Femur - pathology ; Gene Deletion ; Gene Expression Regulation, Enzymologic - genetics ; Gene Knock-out ; Helix-Loop-Helix Transcription Factors ; Homeodomain Proteins - genetics ; Homeodomain Proteins - metabolism ; Homozygote ; Male ; Mice ; Mice, Transgenic ; Notch Pathway ; Organ Size - physiology ; Osteoblast ; Osteoblasts - metabolism ; Osteoblasts - pathology ; Osteoclast ; Osteoclasts - metabolism ; Promoter Regions, Genetic ; Trabecular Microarchitecture ; Transcription Factor HES-1</subject><ispartof>The Journal of biological chemistry, 2011-01, Vol.286 (4), p.2648-2657</ispartof><rights>2011 © 2011 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2011 by The American Society for Biochemistry and Molecular Biology, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c596t-638e8a79dd195ddce7c67786d51da77becece9a33827993e0f39e0c44b94cafb3</citedby><cites>FETCH-LOGICAL-c596t-638e8a79dd195ddce7c67786d51da77becece9a33827993e0f39e0c44b94cafb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024760/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024760/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21084301$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zanotti, Stefano</creatorcontrib><creatorcontrib>Smerdel-Ramoya, Anna</creatorcontrib><creatorcontrib>Canalis, Ernesto</creatorcontrib><title>HES1 (Hairy and Enhancer of Split 1) Is a Determinant of Bone Mass</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>HES1 (hairy and enhancer of split) is a transcription factor that regulates osteoblastogenesis in vitro. The skeletal effects of HES1 misexpression were studied. Transgenic mice where a 3.6-kilobase fragment of the collagen type 1 α1 promoter directs HES1 overexpression were created. Transgenics were osteopenic due to decreased osteoblast function in female and increased bone resorption in male mice. HES1 impaired osteoblastogenesis in vitro, and transgenic osteoblasts enhanced the resorptive activity of co-cultured osteoclast precursors. Mice homozygous for a Hes1 loxP-targeted allele were bred to transgenics, where the paired-related homeobox gene enhancer or the osteocalcin promoter direct Cre recombinase expression to inactivate Hes1 in the limb bud or in osteoblasts. To avoid genetic compensation, Hes1 was inactivated in the context of the global deletion of Hes3 and Hes5. Hes3 and Hes5 null mice had no skeletal phenotype. Hes1 inactivation in the limb bud increased femoral length and trabecular number. Hes1 inactivation in osteoblasts increased trabecular bone volume, number, and connectivity due to increased mineral apposition rate and suppressed bone resorption. Hes1 inactivation in vitro increased alkaline phosphatase expression and suppressed the resorptive activity of co-cultured osteoclast precursors. In conclusion, by inhibiting osteoblast function and inducing bone resorption, HES1 is an intracellular determinant of bone mass and structure.</description><subject>Alkaline Phosphatase - biosynthesis</subject><subject>Alkaline Phosphatase - genetics</subject><subject>Alleles</subject><subject>Animals</subject><subject>Basic Helix-Loop-Helix Transcription Factors - genetics</subject><subject>Basic Helix-Loop-Helix Transcription Factors - metabolism</subject><subject>Bone</subject><subject>Bone Density - physiology</subject><subject>Bone Diseases, Metabolic - genetics</subject><subject>Bone Diseases, Metabolic - metabolism</subject><subject>Bone Diseases, Metabolic - pathology</subject><subject>Bone Formation</subject><subject>Bone Resorption</subject><subject>Cell Differentiation</subject><subject>Cells, Cultured</subject><subject>Coculture Techniques</subject><subject>Collagen Type I - genetics</subject><subject>Collagen Type I - metabolism</subject><subject>Developmental Biology</subject><subject>Enhancer Elements, Genetic - genetics</subject><subject>Female</subject><subject>Femur - metabolism</subject><subject>Femur - pathology</subject><subject>Gene Deletion</subject><subject>Gene Expression Regulation, Enzymologic - genetics</subject><subject>Gene Knock-out</subject><subject>Helix-Loop-Helix Transcription Factors</subject><subject>Homeodomain Proteins - genetics</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Homozygote</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Notch Pathway</subject><subject>Organ Size - physiology</subject><subject>Osteoblast</subject><subject>Osteoblasts - metabolism</subject><subject>Osteoblasts - pathology</subject><subject>Osteoclast</subject><subject>Osteoclasts - metabolism</subject><subject>Promoter Regions, Genetic</subject><subject>Trabecular Microarchitecture</subject><subject>Transcription Factor HES-1</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFPHCEUh4mp0dX23FvLrXoYhYEZ4NKk2rVroulha-KNMPBGMbOwhVkT__uyGWvqwRQOhLyPHw8-hD5SckKJ4KcPnT25ptudZITJHTSjRLKKNfT2HZoRUtNK1Y3cRwc5P5AyuKJ7aL8uFGeEztDZYr6k-GhhfHrCJjg8D_cmWEg49ni5HvyI6TG-zNjg7zBCWvlgwrgtnsUA-Nrk_B7t9mbI8OF5PUQ3F_Nf54vq6uePy_NvV5VtVDtWLZMgjVDOUdU4Z0HYVgjZuoY6I0QHtkxlGJO1UIoB6ZkCYjnvFLem79gh-jrlrjfdCkpAGJMZ9Dr5lUlPOhqvX1eCv9d38VEzUnPRkhLw5Tkgxd8byKNe-WxhGEyAuMlaEc5F-TL1X1KKmtaCKl7I04m0KeacoH_phxK9VaSLIr1VpCdF5cSnf5_xwv91UoDPE9CbqM1d8lnfLOtSIKUzXvQWQk0ElO9-9JB0th6KNecT2FG76N-8_g-bZqdv</recordid><startdate>20110128</startdate><enddate>20110128</enddate><creator>Zanotti, Stefano</creator><creator>Smerdel-Ramoya, Anna</creator><creator>Canalis, Ernesto</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</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>7QP</scope><scope>5PM</scope></search><sort><creationdate>20110128</creationdate><title>HES1 (Hairy and Enhancer of Split 1) Is a Determinant of Bone Mass</title><author>Zanotti, Stefano ; Smerdel-Ramoya, Anna ; Canalis, Ernesto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c596t-638e8a79dd195ddce7c67786d51da77becece9a33827993e0f39e0c44b94cafb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Alkaline Phosphatase - biosynthesis</topic><topic>Alkaline Phosphatase - genetics</topic><topic>Alleles</topic><topic>Animals</topic><topic>Basic Helix-Loop-Helix Transcription Factors - genetics</topic><topic>Basic Helix-Loop-Helix Transcription Factors - metabolism</topic><topic>Bone</topic><topic>Bone Density - physiology</topic><topic>Bone Diseases, Metabolic - genetics</topic><topic>Bone Diseases, Metabolic - metabolism</topic><topic>Bone Diseases, Metabolic - pathology</topic><topic>Bone Formation</topic><topic>Bone Resorption</topic><topic>Cell Differentiation</topic><topic>Cells, Cultured</topic><topic>Coculture Techniques</topic><topic>Collagen Type I - genetics</topic><topic>Collagen Type I - metabolism</topic><topic>Developmental Biology</topic><topic>Enhancer Elements, Genetic - genetics</topic><topic>Female</topic><topic>Femur - metabolism</topic><topic>Femur - pathology</topic><topic>Gene Deletion</topic><topic>Gene Expression Regulation, Enzymologic - genetics</topic><topic>Gene Knock-out</topic><topic>Helix-Loop-Helix Transcription Factors</topic><topic>Homeodomain Proteins - genetics</topic><topic>Homeodomain Proteins - metabolism</topic><topic>Homozygote</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Notch Pathway</topic><topic>Organ Size - physiology</topic><topic>Osteoblast</topic><topic>Osteoblasts - metabolism</topic><topic>Osteoblasts - pathology</topic><topic>Osteoclast</topic><topic>Osteoclasts - metabolism</topic><topic>Promoter Regions, Genetic</topic><topic>Trabecular Microarchitecture</topic><topic>Transcription Factor HES-1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zanotti, Stefano</creatorcontrib><creatorcontrib>Smerdel-Ramoya, Anna</creatorcontrib><creatorcontrib>Canalis, Ernesto</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>AGRIS</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>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zanotti, Stefano</au><au>Smerdel-Ramoya, Anna</au><au>Canalis, Ernesto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HES1 (Hairy and Enhancer of Split 1) Is a Determinant of Bone Mass</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2011-01-28</date><risdate>2011</risdate><volume>286</volume><issue>4</issue><spage>2648</spage><epage>2657</epage><pages>2648-2657</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>HES1 (hairy and enhancer of split) is a transcription factor that regulates osteoblastogenesis in vitro. The skeletal effects of HES1 misexpression were studied. Transgenic mice where a 3.6-kilobase fragment of the collagen type 1 α1 promoter directs HES1 overexpression were created. Transgenics were osteopenic due to decreased osteoblast function in female and increased bone resorption in male mice. HES1 impaired osteoblastogenesis in vitro, and transgenic osteoblasts enhanced the resorptive activity of co-cultured osteoclast precursors. Mice homozygous for a Hes1 loxP-targeted allele were bred to transgenics, where the paired-related homeobox gene enhancer or the osteocalcin promoter direct Cre recombinase expression to inactivate Hes1 in the limb bud or in osteoblasts. To avoid genetic compensation, Hes1 was inactivated in the context of the global deletion of Hes3 and Hes5. Hes3 and Hes5 null mice had no skeletal phenotype. Hes1 inactivation in the limb bud increased femoral length and trabecular number. Hes1 inactivation in osteoblasts increased trabecular bone volume, number, and connectivity due to increased mineral apposition rate and suppressed bone resorption. Hes1 inactivation in vitro increased alkaline phosphatase expression and suppressed the resorptive activity of co-cultured osteoclast precursors. In conclusion, by inhibiting osteoblast function and inducing bone resorption, HES1 is an intracellular determinant of bone mass and structure.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21084301</pmid><doi>10.1074/jbc.M110.183038</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alkaline Phosphatase - biosynthesis Alkaline Phosphatase - genetics Alleles Animals Basic Helix-Loop-Helix Transcription Factors - genetics Basic Helix-Loop-Helix Transcription Factors - metabolism Bone Bone Density - physiology Bone Diseases, Metabolic - genetics Bone Diseases, Metabolic - metabolism Bone Diseases, Metabolic - pathology Bone Formation Bone Resorption Cell Differentiation Cells, Cultured Coculture Techniques Collagen Type I - genetics Collagen Type I - metabolism Developmental Biology Enhancer Elements, Genetic - genetics Female Femur - metabolism Femur - pathology Gene Deletion Gene Expression Regulation, Enzymologic - genetics Gene Knock-out Helix-Loop-Helix Transcription Factors Homeodomain Proteins - genetics Homeodomain Proteins - metabolism Homozygote Male Mice Mice, Transgenic Notch Pathway Organ Size - physiology Osteoblast Osteoblasts - metabolism Osteoblasts - pathology Osteoclast Osteoclasts - metabolism Promoter Regions, Genetic Trabecular Microarchitecture Transcription Factor HES-1 |
title | HES1 (Hairy and Enhancer of Split 1) Is a Determinant of Bone Mass |
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