MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression
Embryonic skeletogenesis and postnatal bone development require the transfer of calcium from the mother to the offspring during pregnancy and lactation. Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an a...
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Veröffentlicht in: | The Journal of biological chemistry 2016-02, Vol.291 (8), p.3959-3966 |
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creator | Kushwaha, Priyanka Khedgikar, Vikram Sharma, Deepika Yuen, Tony Gautam, Jyoti Ahmad, Naseer Karvande, Anirudha Mishra, Prabhat R. Trivedi, Prabodh K. Sun, Li Bhadada, Sanjay K. Zaidi, Mone Trivedi, Ritu |
description | Embryonic skeletogenesis and postnatal bone development require the transfer of calcium from the mother to the offspring during pregnancy and lactation. Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an anabolic phase around weaning during which there is a remarkable recovery of the maternal skeleton. However, the mechanism(s) of this anabolic response remain(s) largely unknown. We identified eight differentially expressed miRNAs by array profiling, of which miR-874-3p was highly expressed at weaning, a time when bone loss was noted to recover. We report that this weaning-associated miRNA is an anabolic target. Therefore, an agomir of miR-874-3p induced osteoblast differentiation and mineralization. These actions were mediated through the inhibition of Hdac1 expression and enhanced Runx2 transcriptional activation. When injected in vivo, the agomir significantly increased osteoblastogenesis and mineralization, reversed bone loss caused by ovariectomy, and increased bone strength. We speculate that elevated miR-874-3p expression during weaning enhances bone formation and that this miRNA may become a therapeutic target for conditions of bone loss. |
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Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an anabolic phase around weaning during which there is a remarkable recovery of the maternal skeleton. However, the mechanism(s) of this anabolic response remain(s) largely unknown. We identified eight differentially expressed miRNAs by array profiling, of which miR-874-3p was highly expressed at weaning, a time when bone loss was noted to recover. We report that this weaning-associated miRNA is an anabolic target. Therefore, an agomir of miR-874-3p induced osteoblast differentiation and mineralization. These actions were mediated through the inhibition of Hdac1 expression and enhanced Runx2 transcriptional activation. When injected in vivo, the agomir significantly increased osteoblastogenesis and mineralization, reversed bone loss caused by ovariectomy, and increased bone strength. We speculate that elevated miR-874-3p expression during weaning enhances bone formation and that this miRNA may become a therapeutic target for conditions of bone loss.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M115.687152</identifier><identifier>PMID: 26663087</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>animal model ; Animals ; bone ; bone morphogenetic protein (BMP) ; Calcification, Physiologic - physiology ; cell differentiation ; Cell Differentiation - physiology ; Core Binding Factor Alpha 1 Subunit - biosynthesis ; Core Binding Factor Alpha 1 Subunit - genetics ; drug discovery ; Epigenesis, Genetic - physiology ; Female ; Gene Expression Regulation, Enzymologic - physiology ; Gene Regulation ; gene silencing ; histone deacetylase 1 (HDAC1) ; Histone Deacetylase 1 - genetics ; Histone Deacetylase 1 - metabolism ; Mice ; microRNA (miRNA) ; MicroRNAs - genetics ; MicroRNAs - metabolism ; osteoblast ; Osteoblasts - cytology ; Osteoblasts - metabolism ; osteoporosis ; Pregnancy ; Weaning</subject><ispartof>The Journal of biological chemistry, 2016-02, Vol.291 (8), p.3959-3966</ispartof><rights>2016 © 2016 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2016 by The American Society for Biochemistry and Molecular Biology, Inc.</rights><rights>2016 by The American Society for Biochemistry and Molecular Biology, Inc. 2016 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-c443t-c241e03f5c0c128c9d6dea3c91a09eeb1143ef1c13360be5309380638249c6e43</citedby><cites>FETCH-LOGICAL-c443t-c241e03f5c0c128c9d6dea3c91a09eeb1143ef1c13360be5309380638249c6e43</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/PMC4759174/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759174/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26663087$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kushwaha, Priyanka</creatorcontrib><creatorcontrib>Khedgikar, Vikram</creatorcontrib><creatorcontrib>Sharma, Deepika</creatorcontrib><creatorcontrib>Yuen, Tony</creatorcontrib><creatorcontrib>Gautam, Jyoti</creatorcontrib><creatorcontrib>Ahmad, Naseer</creatorcontrib><creatorcontrib>Karvande, Anirudha</creatorcontrib><creatorcontrib>Mishra, Prabhat R.</creatorcontrib><creatorcontrib>Trivedi, Prabodh K.</creatorcontrib><creatorcontrib>Sun, Li</creatorcontrib><creatorcontrib>Bhadada, Sanjay K.</creatorcontrib><creatorcontrib>Zaidi, Mone</creatorcontrib><creatorcontrib>Trivedi, Ritu</creatorcontrib><title>MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Embryonic skeletogenesis and postnatal bone development require the transfer of calcium from the mother to the offspring during pregnancy and lactation. Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an anabolic phase around weaning during which there is a remarkable recovery of the maternal skeleton. However, the mechanism(s) of this anabolic response remain(s) largely unknown. We identified eight differentially expressed miRNAs by array profiling, of which miR-874-3p was highly expressed at weaning, a time when bone loss was noted to recover. We report that this weaning-associated miRNA is an anabolic target. Therefore, an agomir of miR-874-3p induced osteoblast differentiation and mineralization. These actions were mediated through the inhibition of Hdac1 expression and enhanced Runx2 transcriptional activation. When injected in vivo, the agomir significantly increased osteoblastogenesis and mineralization, reversed bone loss caused by ovariectomy, and increased bone strength. We speculate that elevated miR-874-3p expression during weaning enhances bone formation and that this miRNA may become a therapeutic target for conditions of bone loss.</description><subject>animal model</subject><subject>Animals</subject><subject>bone</subject><subject>bone morphogenetic protein (BMP)</subject><subject>Calcification, Physiologic - physiology</subject><subject>cell differentiation</subject><subject>Cell Differentiation - physiology</subject><subject>Core Binding Factor Alpha 1 Subunit - biosynthesis</subject><subject>Core Binding Factor Alpha 1 Subunit - genetics</subject><subject>drug discovery</subject><subject>Epigenesis, Genetic - physiology</subject><subject>Female</subject><subject>Gene Expression Regulation, Enzymologic - physiology</subject><subject>Gene Regulation</subject><subject>gene silencing</subject><subject>histone deacetylase 1 (HDAC1)</subject><subject>Histone Deacetylase 1 - genetics</subject><subject>Histone Deacetylase 1 - metabolism</subject><subject>Mice</subject><subject>microRNA (miRNA)</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>osteoblast</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - metabolism</subject><subject>osteoporosis</subject><subject>Pregnancy</subject><subject>Weaning</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFv1DAQRi0EotvCmRvKkUu2ntix4wvSqlooUluktghuluNMFpesE-ykYv99HaVU5YAvI3ueP1vzCHkHdA1U8tO72q4vAcq1qCSUxQuyAlqxnJXw4yVZUVpAroqyOiLHMd7RtLiC1-SoEEIwWskV8ZfOhv76apNVkudsyLZ_MIwxu_mFHY6myzbe1H3nbLZtW7Spsx3cDj2OzpquO2TNFJzfZd_R-LnWh-xmGoaAMc7b88ZYSJnLQe_fkFet6SK-fawn5Nun7e3ZeX7x9fOXs81FbjlnY24LDkhZW1pqoaisakSDhlkFhirEGoAzbMECY4LWWDKqWEUFqwqurEDOTsjHJXeY6j02Fv0YTKeH4PYmHHRvnP63491PvevvNZelAjkHfHgMCP3vCeOo9y5a7DrjsZ-iBikkFRJkldDTBU2DjDFg-_QMUD1b0smSni3pxVK68f757574v1oSoBYA04zuHQYdrUNvsXEhSdBN7_4b_gBufaIP</recordid><startdate>20160219</startdate><enddate>20160219</enddate><creator>Kushwaha, Priyanka</creator><creator>Khedgikar, Vikram</creator><creator>Sharma, Deepika</creator><creator>Yuen, Tony</creator><creator>Gautam, Jyoti</creator><creator>Ahmad, Naseer</creator><creator>Karvande, Anirudha</creator><creator>Mishra, Prabhat R.</creator><creator>Trivedi, Prabodh K.</creator><creator>Sun, Li</creator><creator>Bhadada, Sanjay K.</creator><creator>Zaidi, Mone</creator><creator>Trivedi, Ritu</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160219</creationdate><title>MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression</title><author>Kushwaha, Priyanka ; Khedgikar, Vikram ; Sharma, Deepika ; Yuen, Tony ; Gautam, Jyoti ; Ahmad, Naseer ; Karvande, Anirudha ; Mishra, Prabhat R. ; Trivedi, Prabodh K. ; Sun, Li ; Bhadada, Sanjay K. ; Zaidi, Mone ; Trivedi, Ritu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-c241e03f5c0c128c9d6dea3c91a09eeb1143ef1c13360be5309380638249c6e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>animal model</topic><topic>Animals</topic><topic>bone</topic><topic>bone morphogenetic protein (BMP)</topic><topic>Calcification, Physiologic - physiology</topic><topic>cell differentiation</topic><topic>Cell Differentiation - physiology</topic><topic>Core Binding Factor Alpha 1 Subunit - biosynthesis</topic><topic>Core Binding Factor Alpha 1 Subunit - genetics</topic><topic>drug discovery</topic><topic>Epigenesis, Genetic - physiology</topic><topic>Female</topic><topic>Gene Expression Regulation, Enzymologic - physiology</topic><topic>Gene Regulation</topic><topic>gene silencing</topic><topic>histone deacetylase 1 (HDAC1)</topic><topic>Histone Deacetylase 1 - genetics</topic><topic>Histone Deacetylase 1 - metabolism</topic><topic>Mice</topic><topic>microRNA (miRNA)</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>osteoblast</topic><topic>Osteoblasts - cytology</topic><topic>Osteoblasts - metabolism</topic><topic>osteoporosis</topic><topic>Pregnancy</topic><topic>Weaning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kushwaha, Priyanka</creatorcontrib><creatorcontrib>Khedgikar, Vikram</creatorcontrib><creatorcontrib>Sharma, Deepika</creatorcontrib><creatorcontrib>Yuen, Tony</creatorcontrib><creatorcontrib>Gautam, Jyoti</creatorcontrib><creatorcontrib>Ahmad, Naseer</creatorcontrib><creatorcontrib>Karvande, Anirudha</creatorcontrib><creatorcontrib>Mishra, Prabhat R.</creatorcontrib><creatorcontrib>Trivedi, Prabodh K.</creatorcontrib><creatorcontrib>Sun, Li</creatorcontrib><creatorcontrib>Bhadada, Sanjay K.</creatorcontrib><creatorcontrib>Zaidi, Mone</creatorcontrib><creatorcontrib>Trivedi, Ritu</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</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>Kushwaha, Priyanka</au><au>Khedgikar, Vikram</au><au>Sharma, Deepika</au><au>Yuen, Tony</au><au>Gautam, Jyoti</au><au>Ahmad, Naseer</au><au>Karvande, Anirudha</au><au>Mishra, Prabhat R.</au><au>Trivedi, Prabodh K.</au><au>Sun, Li</au><au>Bhadada, Sanjay K.</au><au>Zaidi, Mone</au><au>Trivedi, Ritu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2016-02-19</date><risdate>2016</risdate><volume>291</volume><issue>8</issue><spage>3959</spage><epage>3966</epage><pages>3959-3966</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Embryonic skeletogenesis and postnatal bone development require the transfer of calcium from the mother to the offspring during pregnancy and lactation. Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an anabolic phase around weaning during which there is a remarkable recovery of the maternal skeleton. However, the mechanism(s) of this anabolic response remain(s) largely unknown. We identified eight differentially expressed miRNAs by array profiling, of which miR-874-3p was highly expressed at weaning, a time when bone loss was noted to recover. We report that this weaning-associated miRNA is an anabolic target. Therefore, an agomir of miR-874-3p induced osteoblast differentiation and mineralization. These actions were mediated through the inhibition of Hdac1 expression and enhanced Runx2 transcriptional activation. When injected in vivo, the agomir significantly increased osteoblastogenesis and mineralization, reversed bone loss caused by ovariectomy, and increased bone strength. We speculate that elevated miR-874-3p expression during weaning enhances bone formation and that this miRNA may become a therapeutic target for conditions of bone loss.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26663087</pmid><doi>10.1074/jbc.M115.687152</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | animal model Animals bone bone morphogenetic protein (BMP) Calcification, Physiologic - physiology cell differentiation Cell Differentiation - physiology Core Binding Factor Alpha 1 Subunit - biosynthesis Core Binding Factor Alpha 1 Subunit - genetics drug discovery Epigenesis, Genetic - physiology Female Gene Expression Regulation, Enzymologic - physiology Gene Regulation gene silencing histone deacetylase 1 (HDAC1) Histone Deacetylase 1 - genetics Histone Deacetylase 1 - metabolism Mice microRNA (miRNA) MicroRNAs - genetics MicroRNAs - metabolism osteoblast Osteoblasts - cytology Osteoblasts - metabolism osteoporosis Pregnancy Weaning |
title | MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression |
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