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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Veröffentlicht in:The Journal of biological chemistry 2011-01, Vol.286 (4), p.2648-2657
Hauptverfasser: Zanotti, Stefano, Smerdel-Ramoya, Anna, Canalis, Ernesto
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Smerdel-Ramoya, Anna
Canalis, Ernesto
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.
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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. 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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><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 &amp; 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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.</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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